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<title>ecancermedicalscience Articles RSS Feed</title>
<link>http://www.ecancermedicalscience.com/</link>
<description>This RSS feed lets you know when new articles are added to the ecancermedicalscience website.</description>
<webMaster>dev@2cs.com;lowens@brandcastmedia.com;linda.cairns@ifom-ieo-campus.it;gordon.mcvie@ieo.it;jonathan@ecancermedicalscience.com;</webMaster>
<language>en</language>
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<title><![CDATA[Safe practice and nursing care of patients receiving oral anticancer medicines: a position statement from UKONS]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2010.177</link>
<pubdate>Tue, 26 Jan 2010 00:00:00 GMT</pubdate>
<description><![CDATA[This position statement has been formulated by oncology nurses from the UK Oncology Nursing Society (UKONS) to provide guidance for nurses on safe practice with oral anticancer medicines. The ultimate aim is to ensure that patients are not only well informed and capable of managing their oral anticancer medicines but also supported safely and effectively while they are receiving these treatments.<br/>]]></description>
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<title><![CDATA[Essential considerations in the investigation of associations between insulin and cancer risk using prescription databases]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.174</link>
<pubdate>Fri, 11 Dec 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Studies of disease outcomes using administrative databases have identified a number of problems with the approach that suggest the need for a high level of expertise in their conduct. This is particularly true in the case of the investigation of the role of different insulins and the risk of cancer, which poses particular issues addressed herein.]]></description>
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<title><![CDATA[The role of funding and policies on innovation in cancer drug development]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2010.164</link>
<pubdate>Wed, 3 Feb 2010 00:00:00 GMT</pubdate>
<description><![CDATA[During the past two decades, cancer incidence has steadily increased due to aging populations, lifestyle and environmental factors, with great personal and national economic consequences. Concurrently, cancer treatments have improved with increased treatment options as well as lengthier disease and disease-free survival rates.<br/><br/>The latest innovation in cancer treatments are targeted biological treatments, joining the current arsenal of surgery, radiotherapy and chemotherapy, particularly significant<br/>in latter stage cancers associated with very poor survival.<br/><br/>Despite this latest breakthrough in cancer treatment, this has in fact only opened the door to beginning to understand the complexity of cancer on a molecular and genetic basis. Oncology research and development (R&D) has the highest failure rate for new molecular entities (NME) and significantly higher development costs. Although tremendous scientific and economic barriers exist, the oncology development market<br/>has increased two-fold over the past five years.<br/><br/>This report aims to map current oncology R&D funding and management, primarily in Europe and the USA, to examine public-private relationships, current oncology R&D strategies and oncology innovation policies. Its objectives are:<br/><br/> - To map current funding and management of oncology R&D via questionnaire<br/>surveys and interviews of oncology experts;<br/> - To produce a high-resolution bibliometric analysis of oncology drug R&D in<br/>order to better understand the public-private mix in research activity;<br/> - To investigate the cumulative life-time funding of specific oncology drugs;<br/> - To review current public policy affecting oncology drug R&D, specifically, public<br/>R&D investment policies, transnational investment policies, regulatory policies,<br/>and drug reimbursement policies; and<br/> - To propose future oncology policies supporting the R&D process.]]></description>
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<title><![CDATA[Imatinib in gastrointestinal stromal tumour (GIST): Northern Cancer Network Experience]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2010.162</link>
<pubdate>Mon, 14 Dec 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Imatinib treatment in metastatic or inoperable gastrointestinal stromal tumours (GIST) has shifted the paradigm of treatment of this disease.  Successful clinical trials of imatinib led to rapid regulatory approval and, in England and Wales, National Institute for Health and Clinical Excellence (NICE) guidance on use of this technology.  NICE recommend detailed audit of their guidelines in clinical practice.  This audit reflects that guidance and was designed to document the use of imatinib in routine clinical practice.  <br/><br/>Methods:  We conducted a retrospective audit of patients with GIST treated with imatinib from 1st February 2002 to 31st March 2007.  Information gathered included patient demographics, disease characteristics, and details of treatment administered, treatment response, toxicities and follow-up data.  The primary objective was to record disease control rate (DCR), defined as a lack of progression on computed tomography (CT) at 3 months.  Secondary end points of this audit were progression-free and overall survival.  These were compared with published clinical trial results.  <br/><br/>Results:  Thirty six consecutive patients with a diagnosis of GIST treated with imatinib were identified.  Median age of patients was 70.1 years.  At the time of analysis, patients have been followed up for a median of 41.6 months.  In total, patients were treated for a median of 15.8 months.  Treatment was generally well tolerated with a small percentage of patients experiencing grade 3/4 toxicities.  Disease control was observed in 30 patients (DCR, 83.3 %, 95% CI 67.2-93.6, intention to treat analysis).  The median progression free survival (PFS) in this cohort was 23.7 months (95% CI 12.9-34.4); while the median overall survival (OS) was 39.7 months (95%CI 22.8-56.5).  <br/><br/>Conclusion: Our data demonstrated that the treatment of unselected GIST patients within the NICE guidance compares favourably to previously published data of randomised registration studies of imatinib.  Of note, the median age of this cohort is some 10 years older than that reported in the trials.  Imatinib was well tolerated with acceptable treatment-related adverse events.<br/>]]></description>
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<title><![CDATA[Preoperative systemic therapy in locally advanced  breast cancer: a single institution experience]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.161</link>
<pubdate>Mon, 12 Oct 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Locally advanced breast cancer (LABC) is common in developing countries and it frequently affects younger women. Patients do very poorly when treated by locoregional therapy alone; therefore, preoperative systemic therapy (PST) is commonly used. Materials and Methods: Medical records of  64 Saudi patients with LABC treated with PST in a single institution were retrospectively reviewed. Results: At diagnosis, most patients were young (median age 41 years), and had poor clinicopathological characteristics. Following surgery, complete pathologic response (pCR) in the breast was achieved in 13 patients (20%). Of 62 patients with known nodal status, 22 (34%) had negative axillary nodes. Presence of estrogen receptor (ER) negative tumor was the only dependent variable that predicted pCR in the breast (P = 0.03). At a median follow-up of 42 months, the median progression-free survival (PFS) was 48 months (95% CI, 20-76 months) and the projected 5-year overall survival (OS) was 68%. The recently published scoring system (J Clin Oncol. 2008 Jan 10;26(2):246-52), was the only variable that independently influenced PFS, while ER negative tumors and presence of lymphovascular space invasion were the only factors that adversely affected OS. Conclusions: Despite the use of standard multimodality approach in the management of patients with LABC, prognosis remains guarded.]]></description>
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<title><![CDATA[Why vitamin D for cancer patients?]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.160</link>
<pubdate>Wed, 30 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Several epidemiological, pre-clinical and clinical studies support Vitamin D as a preventive and therapeutic cancer agent.<br/>Background<br/>Vitamin D and cancer: Calcitriol, the biologically active form of vitamin D (1,25(OH)D), exerts its effects mainly through binding to nuclear vitamin D receptor (VDR). Calcitriol has been shown to be an antiproliferative, prodifferentiation, proapoptotic agent and an inhibitor of cell migration. Animal and human in vitro studies strongly indicate that vitamin D may have benefits for many forms of cancer. Inadequate levels of circulating 25-hydroxy-vitamin D (25(OH)D) are associated with an increased risk and poor prognosis of several types of cancer.<br/>Vitamin D and melanoma: Cutaneous malignant melanoma (CMM) represents a major public health issue: rates in Italy have almost doubled in the last decade and CMM is frequent among young adults. For resected stage II melanoma no standard adjuvant treatment exists and 5-year overall survival is about 70%.<br/>Cultured melanoma cells can synthesise calcitriol from 25(OH)D and express the VDR. Moreover, 1,25(OH)D has antiproliferative and prodifferentiation effects in human melanoma cells. 1,25(OH)D has been shown to induce apoptosis in human melanoma cell lines and has an inhibitory effect on the spreading of melanoma cells in vitro.<br/>Preliminary results on Vitamin D: Epidemiological data indicate that vitamin D deficiency is relatively common in Europe. In an Italian study, we found that 85% of the participants had insufficient levels of 25(OH)D. We have shown through a meta-analysis of randomized trials that vitamin D supplementation is associated with a significant reduction (7%) in total mortality in healthy subjects and an association between VDR and 25(OH)D and CMM progression has also been demonstrated. We have also reported significant associations between VDR polymorphisms and incidence of skin cancer. In early supplementation trials, the lack of effect on cancer incidence has been attributed to insufficient vitamin D supplementation, stressing the need to better study vitamin D bioavailability.<br/>In fact, a recent IARC report highlighted the need for new randomised trials, based on results from our meta-analyses on 25(OH)D serum levels and cancer risk.<br/>Clinical trial and biomarkers studies<br/>In order to assess whether vitamin D supplementation could improve prognosis of CMM, an Italian multicentre trial in stage II resected melanoma patients was planned to monitor changes in 25(OH)D. The study will address two important questions regarding the relationship between the biology of VDR and (i) vitamin D metabolism (ii) CMM prognosis. This will involve investigating the association between VDR polymorphisms and Breslow thickness, the most important prognostic factor of CMM, and between 25(OH)D serum level, vitamin D supplementation and VDR.<br/>We will also evaluate at baseline whether VDR polymorphisms are associated with Breslow thickness and whether we obtain significant increase in 25(OH)D serum levels during the first year of supplementation. We will quantify the percentages of patients who have desirable levels of 25(OH)D and if not the mean time to reach that level. The findings from this study will be of large interest because Vitamin D could have anticancer benefits for a wide spectrum of cancers.]]></description>
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<title><![CDATA[Denis Burkitt and the African lymphoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.159</link>
<pubdate>Wed, 30 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Burkitt's lymphoma has provided a model for the understanding of the epidemiology, the molecular abnormalities that induce tumours, and the treatment of other lymphomas.  It is important to remember that the early phases of this work were conducted in Africa where today, unfortunately, the disease usually results in death because of limited resources, even though most children in more developed countries are cured. This must be changed. In addition, it is time to re-explore, <br/>with modern techniques, some of the questions that were raised some 50 years ago shortly after Burkitt�s first description, as well as new questions that can be asked only in the light of modern understanding of the immune system and the molecular basis of tumor development. The African lymphoma has taught us much, but there is a great deal still to be learned. <br/>]]></description>
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<title><![CDATA[Correlation between administered treatment and patient's Living Will]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.158</link>
<pubdate>Tue, 29 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Respecting the wishes of an adequately informed patient should be a priority in any health structure. A patient with advanced or terminal cancer should be allowed to express their will during the most important phases of their illness. Unfortunately this is seldom the case, and in general instructions regarding an individuals medical care preferences, i.e. their Living Will, expressed when healthy, often change with the onset of a serious illness.<br/>At the European Institute of Oncology (IEO) a clinical study is ongoing to verify whether, during clinical practice, the patient is adequately informed to sign an informed consent, in a fully aware manner, that will allow the patient and doctor to share in the decisions regarding complex treatment strategies (Living Will). A further aim of the study is to verify if health workers, both in hospital and at home, respect the patients will.<br/>The observational study Respecting the patients wishes: correlation between administered treatment and that accepted by the patient in their Living Will was approved by the IEO Ethical Committee in April 2008.<br/>]]></description>
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<title><![CDATA[Role of traditional and new biomarkers in breast carcinogenesis]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.157</link>
<pubdate>Thu, 29 Oct 2009 00:00:00 GMT</pubdate>
<description><![CDATA[During the last decades several biomarkers have been investigated for their possible role as predictors of breast cancer risk, development, prognosis and treatment efficacy.<br/>The discovery of biomarkers strongly associated with breast carcinogenesis has an enormous potential especially for the selection of subjects at high-risk for developing breast cancer who may benefit from chemopreventive treatments.<br/>Although the number of analyzed biomarkers continue to increase, an unique biomarker for breast cancer risk prediction has not been identified and it is more likely that a panel of biomarkers should be taken into account. Anyhow, further studies are needed to validate breast cancer biomarkers evaluation for individual risk assessment.<br/>This review summarizes main biomarkers that have found to have significant roles at different stages of breast carcinogenesis with updates from the more recent literature.]]></description>
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<title><![CDATA[Might salicylate exert benefits against childhood cancer?]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2010.156</link>
<pubdate>Tue, 19 Jan 2010 00:00:00 GMT</pubdate>
<description><![CDATA[Childhood cancers are a broad range of diseases.  Research on the chemopreventive potential of non-steroidal anti-inflammatory drugs (NSAIDs), such as aspirin (acetylsalicylate) has yet to be fully directed to childhood cancers.  A prima facie hypothesis on salicylate and childhood cancer would therefore be based on several factors.  Firstly, salicylate inhibits the production of inflammatory prostaglandins which have been shown to stimulate the growth of cancer cells. Secondly, salicylate inhibits the growth of cancer cells in preclinical models.  Thirdly, salicylate is a natural component of fruits and vegetables so it is consumed within the diet.  Further research, some lines are identified, are recommended.]]></description>
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<title><![CDATA[Oxaliplatin: Preclinical perspectives on the mechanisms of action, response and resistance]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.153</link>
<pubdate>Thu, 24 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Oxaliplatin is a third-generation platinum compound that has shown a wide range of antitumor activity in metastatic cancer and in multiple cell lines. It contains a diaminocyclohexane carrier ligand and is one of the least toxic platinum agents. In the past decade, the use of oxaliplatin for the treatment of colorectal cancer has become increasingly popular because neither cisplatin nor carboplatin demonstrate significant activity. Similar to cisplatin, oxaliplatin binds to DNA leading to GG intrastrand cross-links. Oxaliplatin differs from its parent compounds in its mechanisms of action, cellular response and development of resistance, which are not fully understood.  Like most chemotherapeutic agents, efficacy of oxaliplatin is limited by the development of cellular resistance. ERCC1 (Excision Repair Cross-Complementation group 1) mediated nucleotide excision repair pathway appears to be the major pathway involved in processing oxaliplatin because loss of mismatch repair does not lead to oxaliplatin resistance. Recent findings support the involvement of many genes and different pathways in developing oxaliplatin resistance. This mini-review focuses on the effects of oxaliplatin treatment cell lines with special emphasis to colorectal cell lines.]]></description>
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<title><![CDATA[Detection of a cardiac mass by [18F]FDG-PET/CT: a rare case]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.152</link>
<pubdate>Wed, 19 Aug 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Intra-cardiac masses present an important problem in cardiology. The differential diagnosis includes tumours, which may be primary (benign or malignant) or metastatic, and infected mural thrombi.<br/><br/>Myxomas, sarcomas, breast, lung, and renal cancer represent the commonest causes of primary benign, malignant and metastatic intra-cardiac masses respectively.<br/><br/>Recent studies have shown that cardiac involvement in malignant lymphoma is common but under-investigated.<br/>Diagnostic imaging techniques for detection of cardiac masses include echocardiography, CT and MRI, with echocardiography having the highest sensitivity. We propose that 18-F-PET/CT may play an important role in the detection and evaluation of intra-cardiac masses.<br/><br/>]]></description>
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<title><![CDATA[A parathyroid carcinoma within a cold thyroid nodule]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.150</link>
<pubdate>Fri, 18 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[We report a case of a 71-year-old woman which was referred to our Institute with a solid nodule in the right thyroid lobe and hypercalcemia.<br/>Ultrasound revealed a well-vascularized right thyroid nodule that was identified as a cold area by 99mTc-sodium pertechnetate scan. Fine-needle aspiration showed a follicular lesion and blood tests revealed hypercalcemia and hyperparathyroidism.<br/>A 99mTc-methoxyisobutylisonitrile (99mTc-Sestamibi) scan was subsequently performed revealing a focal area of increased uptake in the right thyroid lobe, within the cold area detected by the thyroid scan.<br/>A right emithyroidectomy and right superior and inferior parathyroidectomy was performed and histopathological examination showed a parathyroid carcinoma (immunohistochemistry positive for PTH and chromogranin A, Ki-67 10%) associated with follicular hyperplasia.]]></description>
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<title><![CDATA[Case mix at the European Institute of Oncology: first report of the Tumour Registry, years 2000-2002]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.149</link>
<pubdate>Wed, 21 Oct 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Introduction: An institutional and centralized hospital-based tumour registry (TR) is the ideal supporting tool for the organization and management of clinical data in a comprehensive cancer center. The purpose of this paper is to describe the development of the TR at the European Institute of Oncology (IEO) in Milan, Italy, from its origin to its current applications.<br/><br/>Material and methods: After a series of meetings with members of administrative, clinical, research and informatics departments, the TR was activated in March 2006 with the aim to collect data on all the individuals referring to the Institute, with or at risk of developing a tumour. It was implemented on an Oracle-based interface. A minimum data set of variables was defined and data collection was divided into four forms, which together gather all the relevant data on patients, tumors, treatments and subsequent events.<br/><br/>Results: After a 6-month pilot period, which involved the training of the tumour registrars, adjustments to the structure of the registry, development of data quality control procedure and finalization of the operative protocol, from September 2006 the data collection has been fully operative. Five registrars have been chronologically entering data of all individuals who visited the IEO for the first time since 1st January 2000. As of March 2009, data on 69,637 individuals and 43,567 tumours has been reviewed, recoded and registered in the TR. Twenty-two percent of the tumors (n=9,578) were first invasive primaries, diagnosed and treated at the IEO; the most common sites were breast (n=4,972), lung (n=627), intestines (n=479) and prostate (n=376).<br/>Conclusion: The IEO TR has proven functional and reliable in monitoring the activity of the Hospital, allowing extraction of data from any subpopulation with characteristics of interest. The structured and centralized TR represents an important tool for our research-oriented Institution.]]></description>
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<title><![CDATA[The evolution of treatment for early breast cancer: what's next?]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.148</link>
<pubdate>Tue, 9 Jun 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Across Europe, the outlook for women diagnosed with early breast cancer is likely to be far better now than at the start of my career. Effective screening programmes mean women are being diagnosed earlier, and greatly improved surgical techniques have also made a significant impact. Post surgery, the evolution of adjuvant therapy has meant that we now have an armoury of effective treatments to stop breast cancer returning, although debate continues on how these treatments should be used for maximum benefit.]]></description>
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<title><![CDATA[Long QT syndrome and torsade de pointes after anthracycline chemotherapy]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.147</link>
<pubdate>Mon, 8 Jun 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Anthracycline chemotherapy, which represents the treatment of choice for many hematologic and metastatic cancers, unfortunately carries with it the possibility of both early cardiotoxic phenomena, occuring during chemotherapy, and also late cardiotoxic manifestations, occuring even months or years from the completion of treatment.<br/><br/>The clinical manifestations of early cardiotoxicity commonly include: ventricular premature beats, supraventricular tachycardia, cardiomyopathy and sudden death.<br/><br/>This study confirms the necessity for close cardiac monitoring of patients undergoing anthracycline therapy. Such monitoring should not only comprise echocardiographic monitoring for left ventricular systo-diastolic dysfunction, but also electrocardiographic monitoring (QTc) in order to exclude electrophysiological changes possibly related to life threatening arrhythmias (10).<br/><br/>]]></description>
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<title><![CDATA[Computerized nuclear morphometry in the diagnosis of thyroid lesions with predominant follicular pattern]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.146</link>
<pubdate>Thu, 17 Sep 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Differential diagnosis of thyroid lesions with predominantly follicular pattern is one of the most common problems in thyroid pathology.  Development of more objective and reproducible tools for diagnosis is needed. This work aimed at studying the role of nuclear morphometry in differential diagnosis of different thyroid lesions having predominant follicular pattern<br/>Material and methods: Semiautomatic image analysis system was used to measure a total of 8 nuclear parameters in 48 thyroid lesions including seven nodular goiter (NG), 14 follicular adenoma (FA), 14 follicular carcinoma (FC) and 13 follicular variant papillary carcinoma (FVPC).<br/><br/>Results: The parameters related to nuclear size (area, perimeter, MaxD, MinD, nuclear size) and shape (L/S ratio, Form_AR) were significantly higher in neoplastic group (FA, FC, FVPC) when compared to non-neoplastic group (NG) P<0.05.  The perimeter was the most reliable parameter (area under the cure (AUC)=97%) followed by area, MaxD, and size (all have AUC= 96%) then form-AR (90%), LS ratio (86%) and the least reliable was Min D (79%). Within the neoplastic group, most parameters related to size and shape of the nuclei was significantly higher in FVPC than in FA and FC (p &#8804; 0.05).  Nuclear area and size (AUC 77%) were the most reliable parameters for differentiation between FVPC and FA.   The best cut off values for diagnosing FVPC are nuclear area &#8805;39.9m2 and nuclear size &#8805;27.7m2.  However, there was no quantitative difference between FC and FA.<br/><br/>Conclusion: Nuclear morphometric parameters may help in the differentiation between neoplastic and non-neoplastic thyroid lesions and between FVPC and follicular neoplasms (FC and FA) but they have no value in the differentiation between FC and FA.<br/><br/><br/><br/>]]></description>
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<title><![CDATA[Cell-cell fusion as a potential target in cancer therapy]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.145</link>
<pubdate>Thu, 6 Aug 2009 00:00:00 GMT</pubdate>
<description><![CDATA[In the fight against cancer, new and more specific targets are needed. Here we offer an example of a potential target that has not been widely studied, namely, the syncytin protein. Syncytin is expressed mainly in the human placenta and is implicated in placental syncytiotrophoblast cell fusion. Not much is known about the role of syncytin in cancer, but the existing data call for more intense research. Its retroviral origins and particular tissue distribution make syncytin an interesting potential target in cancer therapy.]]></description>
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<title><![CDATA[Phase II study of 'high dose' celecoxib and metronomic 'low dose' cyclophosphamide and methotrexate in patients with relapsed and refactory lymphoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.144</link>
<pubdate>Wed, 5 Aug 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Introduction:  Relapsed histologically aggressive non-Hodgkin's lymphoma (NHL) has a poor prognosis; relapsed patients who respond to 2nd line chemotherapy have a better outcome after BMT, while those who don't respond to 2nd line or are unfit for BMT have a worse prognosis and new treatments are needed. Angiogenesis is increased in aggressive NHL and could be targeted by selective cyclooxygenase-2 inhibition and metronomic chemotherapy. <br/><br/>Aim of the study: Assessment of the toxicity of metronomic chemotherapy and the response and progression free survival of relapsed DLCBL patients.<br/><br/>Patients and methods: forty patients with the diagnosis of relapsed and / or refractory DLCBL. Patients included in this study may have received any number of preceding therapies (as long as one had included an Anthracycline) and were not candidates for BMT. They received Cyclophosphamide tab (50 mg p.o. q.d), Methotrexate tab (2.5 mg p.o 4 times/week) and high-dose Celecoxib tab (400 mg p.o. b.i.d.) until disease progression or toxicity.<br/><br/>Results: All of the 40 patients included (median age, 56 years) were evaluable for response, 52% had a high international prognostic index at relapse, with a median follow-up of 8.4 months (range 4-23 months),<br/>32.5 % had a partial response and 50% has stable disease. Progression-free survival was 12 months. The median response duration was 9 months. Treatment protocol was well tolerated with no major toxicities. The most common toxicity was fatigue (57.5%), myelo-suppression and gastrointestinal side effects.<br/><br/>Conclusions: Low-dose Cyclophosphamide, Methotrexate and high-dose Celecoxib is well tolerated and active in pretreated diffuse large cell B lymphoma. Although thrombotic events were not observed during this study, Close surveillance for arterial and venous thrombotic events is recommended.<br/><br/>]]></description>
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<title><![CDATA[Intraprostatic fiducial markers: a potential application for ultrasound-guided radiotherapy in prostate cancer]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.143</link>
<pubdate>Tue, 12 May 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Report on a two-phase test performed to assess the ability of the ultrasound-based B-mode Acquisition and Targeting (BAT) trans-abdominal system to identify non-dedicated fiducial markers implanted into the prostate gland for subsequent image-guided-radiotherapy.<br/><br/>Although further investigation is warranted in order to identify the optimal echogenic marker and to define its potential use for image-guided-radiotherapy in prostate cancer patients, we demonstrate the feasibility of the BAT system for the visualization of non US-dedicated markers. <br/>]]></description>
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<title><![CDATA[Comparison between endoscopic and surgical treatment of screen-detected vs. non-screen-detected colorectal cancers]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.142</link>
<pubdate>Tue, 12 May 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Since 2005 the Italian National Health System (NHS) has implemented a screening program for colorectal cancer for all citizens over 50. Screening tests are free for the target population (so called "Minimal Care Level" guaranteed for all Italian citizens). Invitees are asked to take an immunological test for Faecal Occult Blood (FOBT) every 2 years. Individuals with a positive FOBT test are invited to undergo a total colonoscopy in an SSN-accredited Endoscopy Department.<br/><br/>Each Italian Region has a Centre for the coordination of the screening program which employs a dedicated software that can trace the course of each citizen within the program.<br/><br/>The "Screening Centre" has a database that can provide a detailed, real-time situation of the program: it is therefore possible to compare the characteristics of screen-detected and non-screen-detected cancers.<br/><br/>The target population for the screening program includes all citizens aged 50 to 70, except "high-risk" subjects [family history; serious, persistent IBD; previous colorectal surgery; recent non-screen-related FOBT and/or colonoscopy; apparent digestive-tract symptoms (proctorrhagia; abdominal pain; bowel irregularities, etc.)].]]></description>
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<title><![CDATA[Report of the EORTC-PAMM Meeting, Brussels, March 16-18th, 2009]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.141</link>
<pubdate>Thu, 2 Apr 2009 00:00:00 GMT</pubdate>
<description><![CDATA[For the first time, the 2009 Pharmacology and Molecular Mechanisms (PAMM) winter meeting was organized in connection with the EGAM (EORTC Groups Annual Meeting) in Brussels. Furthermore, the PAMM participated in an additional plenary session together with the PathoBiology Group (PBG) and the functional imaging group during the EGAM itself, in which the Laboratory Research Division (LRD) summarized their expertise in translational research and gave an overview of what it can offer to the Disease Oriented Groups (DOGs). The emphasis of the joint meeting was on novel concepts in cancer treatment and on new approaches to monitor therapy and implement personalized strategies.<br/><br/>Three main subtopics that could be possibly canvassed out of whole meeting, namely: a) apoptosis and signaling, b) cancer stem cells, c) cancer genome and epigenome profiling.<br/>]]></description>
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<title><![CDATA[Male breast cancer: A review]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.140</link>
<pubdate>Fri, 20 Mar 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Male breast cancer (MBC) is rare, with the peak age of onset at 71 years.  BRCA2 mutations are more frequent than BRCA1 with 20% of cases giving a family history. Risk factors for MBC are poorly understood and include working in high ambient temperatures and exhaust fume exposure. MBC is associated with hyperestrogenic states found in liver disease, Klinefelter?'s syndrome, gonadal dysfunction or obesity.  Most information on treatment of MBC is derived from large randomised trials carried out in female patients. The small numbers of MBC seen in any unit annually has precluded significant  trials being carried out.  <br/><br/>Diagnosis and treatment of MBC is similar to that of female patients but men tend to be treated with mastectomy rather than breast conserving surgery. The mainstay of adjuvant therapy or palliative treatment for advanced disease is endocrine, mostly tamoxifen. Prognosis of male patients is equal to that of stage-matched women, but men tend to fare worse because of delay in presentation leading to a large proportion of patients presenting with stage III or IV disease. Increased input is needed for psychological support for male breast cancer patients. Specific therapeutic questions about MBC need international trials to obtain meaningful answers.]]></description>
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<title><![CDATA[Laboratory-based management of microbiological alerts: Effects of an automated system on the surveillance and treatment of nosocomial infections in an oncology hospital]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.137</link>
<pubdate>Tue, 31 Mar 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Prevention and surveillance programs are key to contain Nosocomial Infections (Nis).  At the European Institute of Oncology, surveillance based on ex-post data collection has always been done since the inception of hospital activity; laboratory-based surveillance of microbiological alert was not standardized. This study describes the issues related to the recent introduction in hospital routine of a laboratory-based automated surveillance system and its clinical impact on monitoring and treatment of Nis.<br/><br/>Methods: An interdisciplinary team defined the alerts and the actions to be taken in response; recipients of the alert messages were identified and software was programmed. Program features were created so their employment would generate a prompt notification of clinically critical results. After a training period, the program was introduced in the hospital routine.<br/><br/>Results: There were a total of 150 generated alerts; the main alert related to microorganisms requiring prompt patient isolation and/or public notification. Clinical use of the program was relevant in detection and immediate notification of Cytomegalovirus active infection in stem cell recipients and central venous catheter  related candidemia: the prompt administration of adequate treatment was possible hours in advance compared to the previous approach. <br/>Conclusions: A laboratory-based automated surveillance system is effective in facilitating the management of NIs; its clinical employment also leads to important clinical advantages in patient care.<br/>]]></description>
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<title><![CDATA[Is there a role for 'modified VAD' in the treatment of multiple myeloma?]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.136</link>
<pubdate>Thu, 4 Jun 2009 00:00:00 GMT</pubdate>
<description><![CDATA[BACKGROUND In recent years the popularity of VAD has been tempered but we believe it still has a role in a particular patient group. The aim of our study was to demonstrate if lower doses of drugs in VAD could reduce toxicity without affecting efficacy. METHODS From January 1997 to January 2007, 56 previously untreated multiple myeloma patients were treated with 'modified VAD': a continuous infusion of Vincristine (0.4mg/sqm)and Doxorubicin (9mg/sqm) on days 1 to 3 and Dexamethasone 40mg for 5 consecutive days (iv on days 1  to 3 and then orally on days 4 and 5). RESULTS  According to the Blad et al. criteria, the overall response rate (CR, nCR, VGPR, PR) was 60%: CR and nCR10%, VGPR and PR 50%, SD 40%. This regimen was well tolerated.CONCLUSIONS In our experience, the modified VAD maintains its validity in older untreated or relapsed patients. However in light of newer thalidomide-based combination therapies, which have higher response rates and are better in mobilizing stem cells the role of VAD has changed.]]></description>
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<title><![CDATA[Communication skills and raising awareness in clinical practice: An Italian experience]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.135</link>
<pubdate>Wed, 11 Feb 2009 00:00:00 GMT</pubdate>
<description><![CDATA[The importance of communication as an essential component of healthcare is widely accepted throughout the literature. Its importance is especially relevant when dealing with patients with a cancer diagnosis, who may be facing difficult or complex decisions about treatment options and end of life care issues. Despite acceptance of its value, research has indicated continuing dissatisfaction with communication skills. Although several counties have made recommendations towards integration of communication skills training for healthcare professionals caring for patients with cancer, this is not mandatory. <br/><br/>Using reflection on clinical practice, a pilot project was undertaken to look at staff perceptions of communication skills, best practice methods and training opportunities within a haemato-oncology unit in a cancer hospital in Italy. A questionnaire was distributed to medical and nursing staff members of the unit (n=32) and focused on communication practice, information giving, difficult situations and training. Forty-three percent of staff responded. The global perception of overall effectiveness of communication skills of the responders regarding communication of diagnosis, prognosis and condition was high. Practical aspects of giving information about disease, prognosis and treatment to patients and relatives, were highlighted in terms of the importance of environment - type and availability, having the personnel necessary for this type of communication and patient choice. Different methods and techniques for communication were reported, however this appeared independent of medical or nursing background, and time in clinical practice. The overall, the views of the team (stratified), showed no great difference between years of practice or profession. This projects has been fundamental in raising awareness of the issue of communication and encouragement of reflection on daily practice in order to give some direction for service development, in an area where the need for communication skills training is not currently seen as mandatory but may be beneficial not only for patients but staff well-being.<br/><br/>Areas for our future practice development include training, addressing environmental issues, team-working and developing written information to support verbal information.<br/>]]></description>
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<title><![CDATA[A competency based educational programme for research nurses: An Italian experience]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.134</link>
<pubdate>Wed, 18 Mar 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Background The EU Directive states the requirement of staff working in trials to be qualified by education, training and experience [14]. This includes the research nurse, however, in the transition from ward nurse to research nurse, new and highly developed skills and knowledge are required in order to work effectively. <br/><br/>Methods An educational programme was developed, which included a review of current knowledge and baseline practice, development of competencies related to the role of research nurse, haemato-oncology and clinical trial education to support this advanced practice for nurses in clinical trials. <br/><br/>Results Overall, the feedback on the course by the nurses was very positive, and the nurses were able to undertake the role of research nurse within specified clinical trials<br/><br/>Conclusions The role of the research nurse is complex and varied. First level nurse training does not cover all aspects for the performance and skills required for this role. By assessing the practice environment and requirements of nurses working in clinical trials, it was possible to recognise previous education, skills and knowledge of the nurses and develop a programme to complement this. Job specific training and competencies have been helpful in clarifying and defining key areas of a previously poorly defined role, and have assisted these nurse in performing as research nurses within in clinical trials.<br/>]]></description>
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<title><![CDATA[Detection of Methylation in the CpG islands of the P<sup>16INK4A</sup>, RASSF 1A and Methyl-Guanine Methyl-Transferase (MGMT) gene promoters in Pancreatic Adenocarcinoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.131</link>
<pubdate>Thu, 15 Jan 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Pancreatic cancer consists of an accumulation of genetic and epigenetic alterations. Recently, aberrant methylation of CpG islands of cancer-related genes has emerged as an important epigenetic mechanism of their transcriptional dysregulation during tumour development. <br/><br/>Therefore, new diagnostic methods, for early detection based on a better understanding of the molecular biology of pancreatic cancer, are required.<br/><br/>We examin the methylation status of p16INK4A, RASSF 1A and MGMT genes considered to be inactivated by promoter methylation in several tumours.]]></description>
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<title><![CDATA[QTc prolongation assessment in anticancer drug development: Clinical and methodological issues]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.130</link>
<pubdate>Mon, 12 Jan 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Cardiac safety assessments are commonly employed in the clinical development of investigational oncology medications. In anticancer drug development there has been increasing consideration for the potential of a compound to cause adverse electrocardiographic changes, especially QT interval prolongation, which can be associated with risk for torsades de pointes and sudden death. Irrespective of overt clinical toxicities, QTc assessment can potentially influence decision making at many levels during the conduct of clinical studies, including eligibility for protocol therapy, dose delivery or discontinuation, and analyses of optimal dose for subsequent development. Given the potential for serious and irreversible morbidity from cardiac adverse events, it is understandable that cardiac safety results can have broad impact on study conduct and patient management. The methodologies for risk management of QTc prolongation for non cardiac drugs have been developed out of experiences primarily from drugs used to treat non life-threatening illnesses in a chronic setting such as antibiotics or antihistamines. Extrapolating these approaches to drugs for treating cancer over an acute period may not be appropriate. Few specific guidelines are available for risk management of cardiac safety in the development and use of oncology drugs. In this manuscript, clinical and methodological issues related to QTc prolongation assessment will be reviewed. Discussions about limitations in phase I design and oncology drug development will be highlighted. Efforts are needed to refine strategies for risk management, avoiding unintended consequences that negatively affect patient access and clinical development of promising new cancer treatments. A thoughtful risk management plan generated by an organized collaboration between oncologists, cardiologists, and regulatory agencies to support a development program essential for oncology agents with cardiac safety concerns.<br/><br/>]]></description>
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<title><![CDATA[Distinct pattern of mutations of conserved regions of TP53 in colorectal cancer patients in  the Kashmiri population: An emerging high risk area]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.129</link>
<pubdate>Fri, 9 Jan 2009 00:00:00 GMT</pubdate>
<description><![CDATA[BACKGROUND: Colorectal cancer is (CRC) one of the leading causes of mortality and morbidity. The kashmir valley, in northern India, has been described as a high risk area for colorectal cancer. AIM: The aim was to make a preliminary attempt to study mutations in exons 5-8 (the DNA binding domain) of the tumour suppressor gene TP53, in 42 CRC patients from Kashmir. MATERIALS AND METHODS: The study population consisted of 42 patients diagnosed with colorectal cancer. Mutations in exons 58 of the TP53 gene were detected by means of single strand conformation polymorphism (SSCP). All samples which showed different band migration patterns in the SSCP were confirmed by sequencing. RESULTS: The 28 mutations were found in the TP53 gene in 19 patients, comprised 23 substitutions (17 transitions + 6 transversions), and five insertions. The 23 substitutions represent 18 missense mutations, leading to amino acid substitutions, 2 nonsense mutations leading to stop codons, while the remaining 3 were silent mutations. The five insertions represented frame-shifts. Two of 28 mutations (7.14%) have not been previously reported in colon cancer samples and were identified as novel TP53 mutations. Comparison of the mutation profile with other ethnic populations and regions reflected both differences and similarities indicating co-exposure to a unique set of risk factors. CONCLUSIONS: Mutation of the TP53 gene is one of the commonest genetic changes in the development of human colorectal cancer. The high frequency of TP53 gene mutations implicates TP53 as a predominant factor for colorectal cancer in the high risk ethnic Kashmiri population.]]></description>
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<title><![CDATA[Overexpression of c-Myc oncoprotein in oral squamous cell carcinoma in the south Indian population]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.128</link>
<pubdate>Mon, 23 Feb 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Oral neoplasm constitutes a predominant class of cancer that is encountered in South India. This is in large part due to the elevated risk of oncogenesis as a result of the habit of chewing of quids containing betel leaves, areca nut and smokeless tobacco. An array of molecular events are induced during the transformation of the buccal epithelium, among them the over-expression of oncogene products.<br/><br/>c-Myc protein, a regulator of a number of key cellular signaling pathways, plays a pivotal role in a number of malignancies.  The present study was undertaken to evaluate expression of c-Myc protein in tumors of the oral cavity from the South Indian population,that are predominantly oral squamous cell carcinoma (OSCC). c-Myc protein was overexpressed in 80% of the cases studied.  <br/><br/>Taking into account the pivotal role demonstrated for c-Myc in tumorigenesis as well as its potential as a therapeutic target, our observations suggest a key role in the genesis of OSCC in this population. <br/>]]></description>
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<title><![CDATA[Cardio-oncology: A new medical issue]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.126</link>
<pubdate>Mon, 15 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Due to the increasing number of long-term cancer survivors, the ageing of the population, as well as the increased incidence and prevalence of oncologic and cardiovascular diseases, the number of patients presenting oncologic and cardiologic comorbidities are increasing. Accordingly, there is a rapidly growing need for a comprehensive and proficient management of patients in whom the two comorbidities exist, and for cancer patients whose clinical history and oncologic treatment put them at higher risk for developing cardiovascular problems, in order to provide the optimal treatment in every situation, and to avoid the possibility that the development of the second disease does not lead to a reduction of therapeutic opportunities for the patient. A new discipline, Cardioncology, has been created to deal with this need. Its aim is to investigate new strategies, collect new evidence-based indications, and develop interdisciplinary expertise in order to manage this growing category of patients. Cardioncology deals with the following main clinical and research areas: Early diagnosis of cardiotoxicity, risk stratification and preventions, treatment and monitoring of cardiotoxicity.]]></description>
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<title><![CDATA[Sentinel lymph node biopsy: Technique validation at the Setbal Medical Centre - Portugal]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.124</link>
<pubdate>Thu, 15 Jan 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Aims: To evaluate the accuracy of sentinel lymph node biopsy in breast cancer patients at this institution, using combined technetium-99m (99mTc) sulphur colloid and patent blue vital dye.<br/>Methods: From March 2007 to July 2008, 50 patients with a tumour less than 3cm with clinically negative axillary lymph nodes underwent sentinel lymph node biopsy (SLNB) followed by axillary lymph node dissection (ALND). Subareolar 99mTc sulphur colloid injection was performed the day before surgery and patent blue vital dye was also injected subareolarly at least 5 minutes before surgery. Sentinel lymph node was identified during the surgical procedure using a gamma probe and direct vision. All sentinel nodes underwent frozen section analysis. Later haematoxylin & eosin staining and immunohistochemical analysis were performed. Finally, SLNB was compared with standard ALND for its ability to accurately reflect the final pathological status of the axillary nodes.<br/>Results: The sentinel lymph node (SLN) was identified in 48 of 50 patients (96%). The number of sentinel lymph nodes ranged from 1-4 (mean 1.48) and non sentinel nodes ranged from 7-27 (mean 14.33). Of the 48 patients with successfully identified SLNs, 29.17% (14/48) were histologically positive. Sensivity of the SLN to predict axilla was 93.75%; accuracy was 97.96%. The SLN was falsely negative in one patient  6.25% (1/16).<br/>Conclusions: This validation study proves the accuracy of the SLNB and its reasonable false negative rate. The SLNB represents a major advance in the surgical treatment of breast cancer as a minimally invasive procedure predicting the axillary lymph node status and can now be used as the standard method of staging in patients with early breast cancer at this institution.]]></description>
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<title><![CDATA[A screening and prevention program serving an ethnically diverse population of women at high risk of developing breast and/or ovarian cancer]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.123</link>
<pubdate>Mon, 16 Mar 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Introduction: We describe a screening and prevention program primarily targeting underserved minority women at high risk of breast and/or ovarian cancer. Women attending this Bellevue Hospital Center (BHC) clinic were either self-referred from a variety of special outreach programs or referred internally by medical professionals caring for relatives or friends. Our objective was to delineate referral sources and preliminary risk-assessment findings in relation to demographic features in this population. <br/><br/>Methods:  Following a detailed family and personal history intake and physical exam, each woman on their initial visit is categorized into low (standard) risk, high, and indeterminate risk groups.  Women found to be at high risk of developing breast and/or ovarian cancer are referred for further testing, additional screening measures, or participation in chemoprevention trials. All other women are counseled concerning follow-up and life style issues.<br/><br/>Results:  Between 2003 and 2007, 171 women for whom complete information was obtained, were analyzed. Thirty four of the women were Caucasians (19.8%) and 137 (80.2%) were ethnically diverse minority women. Sixty two (36.2%) were found to be at high risk with a median age of 42 years. The majority of the high risk women were referred to the clinic by medical professionals (58%), most of which were from within the BHC health care system.  Trends in genetic testing results indicate fewer mutations among high risk Asians than among other ethnicities.<br/><br/>Conclusion:  Accurate risk assessments and implementation of screening and prevention measures have been challenging during the first few years of operation. Nevertheless, the need for providing consultation from internal referrals, and the potential for genetic and psychosocial research in an ethnically diverse population are powerful incentives for continuing to evolve these services. <br/>]]></description>
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<title><![CDATA[Azacitidine prolongs overall survival and reduces infections and hospitalisations in patients with WHO-defined acute myeloid leukaemia compared with conventional care regimens: An update]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.121</link>
<pubdate>Wed, 10 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Azacitidine (AZA), as demonstrated in the phase III trial (AZA-001), is the first MDS treatment to significantly prolong overall survival (OS) in higher-risk MDS patients (pts) (Blood 2007; 110:817). Approximately one third of the pts enrolled in AZA-001 were FAB RAEB-T (&#8805;20%-30% blasts) and now meet the WHO criteria for acute myeloid leukaemia (AML) (Blood 1999;17:3835). Considering the poor prognosis (median survival <1 year) and the poor response to chemotherapy in these pts, this subgroup analysis evaluated the effects of AZA vs conventional care regimens (CCR) on OS and on response rates in pts with WHO AML.]]></description>
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<title><![CDATA[The effects of continued azacitidine treatment cycles on response in higher-risk patients with myelodysplastic syndromes: An update]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.118</link>
<pubdate>Mon, 8 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The international, phase III, multicenter AZA-001 trial demonstrated azacitidine (AZA) is the first treatment to significantly extend overall survival (OS) in higher-risk Myelodysplastic Syndromes (MDS) patients (Fenaux, Blood 2007;110:817). The current treatment paradigm, which is based on a relationship between complete remission (CR) and survival, is increasingly being questioned (Cheson, Blood 2006;108:419). Results of AZA-001 show CR is sufficient but not necessary to prolong OS (List, J Clin Oncol 26:2008;abstr 7006). Indeed, the AZA CR rate in AZA-001 was modest (17%), while partial remission (PR, 12%) and haematologic improvement (HI, 49%) were also predictive of prolonged survival. This analysis was conducted to assess the median number of AZA treatment cycles associated with achievement of first response, as measured by IWG 2000-defined CR, PR, or HI (major + minor). The number of treatment cycles from first response to best response was also measured.]]></description>
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<title><![CDATA[Breast reconstruction after nipple/areola-sparing mastectomy using cell-enhanced fat grafting]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2009.116</link>
<pubdate>Fri, 5 Jun 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Success of fat grafting in breast reconstruction depends on fat retention. The use of stem cells enriched fat graft is an alternative method for graft stability.<br/><br/>Case Report: A case of nipple-areola sparing mastectomy double stage reconstruction with the use of stem cells enhanced fat graft is reported.<br/><br/>Conclusions: Fat grafting is growing like a new and promising tool in the reconstruction of nipple and areola sparing mastectomies in the way to restore a sufficient and reliable subcutaneous space in the mastectomy flap. This combined with an anatomical gel implant offer a integrated system to achieve a natural shaped breast.]]></description>
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<title><![CDATA[Molecular characterisation of signalling pathways in cancer stem cells]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.115</link>
<pubdate>Tue, 2 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[To avoid artifacts introduced by culturing cells for extended periods of time, it is crucial to use low-passage patient-derived tumour cells. The ability to enrich, isolate and assay subpopulations of cells that behave as cancer stem cells (CSCs) from these primary cell lines is essential before performing characterizations such as gene expression profiling. We have isolated cells from glioblastomas which show characteristics of CSCs. Although glioblastomas contain only a relatively small amount of putative CSCs, these cells express many genes which seem to be worthy targets for future therapies.]]></description>
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<title><![CDATA[Cancer stem cells in melanoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.114</link>
<pubdate>Mon, 1 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The identification of cancer stem cells in various malignancies led to the hypothesis that these cells have the exclusive ability of self-renewal, contribute to the plasticity of the tumors and may be the cause for ineffective cancer therapies. Several markers of melanoma stem cells have been described in recent studies including CD133, CD166 [1], Nestin and BMI-1 2. Further studies are necessary to identify, better define, and understand origin and function of cancer stem cells. If confirmed that cancer stem cells play an important role in malignancy, therapeutic strategies may need to be redirected towards these cells to circumvent the failure of conventional therapies.<br/><br/>]]></description>
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<title><![CDATA[Pegylated Liposomal Doxorubicin (PLD): Enhanced skin toxicity in areas of vitiligo]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.111</link>
<pubdate>Tue, 9 Dec 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Pegylated liposomal doxorubicin (PLD; Doxil; Caelyx) is widely used for the treatment of ovarian cancer. It is a stable formulation encapsulating doxorubicin in a "Stealth" (i.e., pegylated) liposome with a half-life of about 72 hours. This drastically altered pharmacology confers to it a considerably lower risk of cardiotoxicity, no acute emesis, and near absence of alopecia or problems with extravasation necrosis. On the other hand, PLD's dose-limiting toxicity is cutaneous1. Since the original phase I report2, cutaneous toxicities reported with PLD fall into four common categories: the well known hand-foot syndrome (also called palmoplantar erythrodysesthesia, or PPE), a diffuse follicular rash, intertrigo-like eruption, and hyperpigmentation including melanotic macules.]]></description>
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<title><![CDATA[Co-existence of breast and ovarian cancers in BRCA germ-line mutation carriers]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.109</link>
<pubdate>Tue, 25 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Abstract:<br/>The co-existence of breast and ovarian cancers in the same individual should raise suspicion of a hereditary process.  Patients with either BRCA1 or BRCA2 germline mutations have an average risk of 39% and 11% respectively of developing ovarian cancer by the age of 70 they have a risk of 35-85% of developing breast cancer in their lifetime .  We report here unusual pathologic features in a BRCA2 germ-line mutation carrier recently diagnosed with synchronous breast and ovarian cancers, and summarize the findings in 6 other women who were diagnosed with ovarian cancer either simultaneously with the diagnosis of breast cancer or at varying times after the diagnosis.  While in most instances this may be a coincidental occurrence in highly susceptible individuals, the patient we highlight raises the provocative hypothesis that at times breast cancer metastasizes to the ovaries of mutation carriers and stimulates the development of an ovarian cancer as well as other cancers.  In addition, these ovarian cancers may have different mechanisms of metastases predisposing them to travel to unusual sites.  <br/>]]></description>
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<title><![CDATA[A randomised trial evaluating Bevacizumab as adjuvant therapy following resection of AJCC stage IIB, IIC and III cutaneous melanoma: An update]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.108</link>
<pubdate>Wed, 12 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[At present there are no standard therapies for the adjuvant treatment of malignant melanoma. Patients with primary tumours with a high Breslow thickness (stages IIB and IIc) or with resected loco-regional nodal disease (stage III) are at a high-risk of developing metastasis and subsequent disease-related death. Given this, it is important that novel therapies are investigated in the adjuvant melanoma setting. Since angiogenesis is essential for primary tumour growth and the development of metastasis, anti-angiogenic agents are attractive potential therapeutic candidates for clinical trials in the adjuvant setting. Therefore, we initiated a Phase II trial in resected high-risk cutaneous melanoma assessing the efficacy of bevacizumab versus observation.<br/><br/>In the interim safety data analysis, we demonstrate that bevacizumab is a safe therapy in the adjuvant melanoma setting with no apparent increase in the surgical complication rate after either primary tumour resection and/or loco-regional lymphadenectomy.<br/> <br/><br/>]]></description>
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<title><![CDATA[Phase 0 workshop at the 20th EORTC-NCI-AACR symposium, Geneva]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.107</link>
<pubdate>Wed, 12 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Are Phase 0 clinical trials really necessary?<br/><br/>This question was posed by James Doroshow (National Cancer Institute, Bethesda, US) at the 20th EORT-NCI-AARC symposium on Molecular Targets and Cancer Therapeutics (Geneva, 21-24 October 2008). Together with E. Leo (Beerse, Belgium), James Doroshow - since 2004 Director of the Division of Cancer Treatment and Diagnosis at NCI- was co-chairing the workshop on Phase 0 clinical trials. In his introduction to the speakers, Doroshow raised six open questions, namely whether Phase 0 trials are useful, ethically acceptable, feasible, whether they speed up the drug development process and save money, and whether there is room for improvement.]]></description>
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<title><![CDATA[SPECT/CT 90Y-Bremsstrahlung images for dosimetry during therapy]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.106</link>
<pubdate>Tue, 11 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background: The characteristics of 90Y, suitable for therapy, are demoted by the lack of -emission. Alternative methods, using analogues labelled with 111In or 86Y, are generally applied to image 90Y-conjugates, with some inevitable drawbacks. New generation SPECT/CT image systems offer improved Bremsstrahlung images. Intent of this brief communication is to show that high quality 90Y-Bremsstrahlung SPECT-CT images can be obtained, allowing to evaluate the biodistribution of pure -emitter therapeutical agents, also during the course of therapy.<br/><br/>Methods: The hybrid system Siemens Symbia-T2 was used for the acquisition of a patient administered with 1.7 GBq of 90Y-DOTATATE. The following parameters were set for SPECT: 80(50%) keV and 120(30%) keV energy windows medium energy collimators 128x128 matrix, 64 projections (40s/step). Low-dose CT was acquired (80mAs) for attenuation correction. Images were reconstructed with the OSEM 3D-Fast algorithm. <br/><br/>Results: Post-therapy SPECT-CT 90Y-Bremsstrahlung images of a patient undergoing receptor peptide radionuclide therapy are presented. 90Y-Bremsstrahlung images obtained are suitable for tumour and normal organ dosimetry, offering detailed information on biodistribution, comparable to 111In-diagnostic images.<br/><br/>Conclusions: The improvement on Bremsstrahlung images allows to address diagnostic examinations to patient recruitment and to restrict ample dosimetry evaluation only to treated patients. This could avoid the need of a different radionuclide or isotope to mimic therapy. The clinical impact might be notable, being dosimetry and toxicity information essential in radionuclide therapy especially in patients with risk factors.<br/><br/>]]></description>
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<title><![CDATA[Does neoadjuvant chemotherapy increase breast conservation in operable breast cancer: an Egyptian experience]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.104</link>
<pubdate>Thu, 9 Apr 2009 00:00:00 GMT</pubdate>
<description><![CDATA[Introduction: The role of adjuvant chemotherapy in breast cancer is well established as are the indications. Likewise the role of neoadjuvant chemotherapy in locally advanced breast cancer is well established. The use of neoadjuvant chemotherapy in operable breast cancer has only recently become of interest to researchers.<br/><br/>Patients and methods: This study included 34 cases of operable breast cancer that were given 4 cycles of neoadjuvant chemotherapy in the form of FEC100 then subjected to surgery. Surgery done was either breast conserving surgery (BCS) or modified radical mastectomy. All patients completed the treatment regimen and no patients were excluded from the study. All surgical specimens were studied pathologically for chemotherapy effect.<br/><br/>Results: An overall objective response was observed in 70.6% of the patients. Seven patients (20.6%) experienced a clinical complete response (cCR), seventeen patients (50.0%) had partial response , nine patients (26.5%) had no change of their disease, and only one patient had disease progression. Of the seven patients who had a cCR, only four patients (11.8%) had pathologic complete response (pCR), while pCR for the whole group was14.7 %( 5/34). Tumor size of more than 2 cm was observed in 28patients (82.4%) at time of presentation, while tumor size of 2 cm or less was seen in 6 patients (17.6%) only. After completion of the course of chemotherapy, twenty three patients (67.6%) were observed to have tumors of 2 cm or less that allowed for less extensive resections. Twenty three patients underwent breast conservative surgery (67.6%) while modified radical mastectomy was performed in 11 patients (32.4%).<br/><br/>Conclusion: : The use of neoadjuvant chemotherapy in operable breast cancer in this study was associated with tumor and axillary downstaging which increased the proportion of cases undergoing breast conservation, with acceptable side effects and reasonable cost. During the limited follow up time of this study no loco regional recurrences were observed and one distant treatment failure was recorded. Its impact, if any, on overall or disease-free survival is still ongoing.<br/> <br/>]]></description>
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<title><![CDATA[Gemcitabine-induced progressive and sustained tumour response  in a patient with multi-drug resistant uterine leiomyosarcoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.102</link>
<pubdate>Mon, 24 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Despite the combination of gemcitabine (GCB) and docetaxel showed a benefit on disease-free survival and overall survival than GCB alone in patients with soft tissue sarcoma, GCB mono-chemotherapy should be a preferable option respect with the combination, because of its lower toxicity profile and its possibility to be administered continuously for a long-time period.<br/><br/>Case Report: We report a clinical case of a woman with advanced high grade uterine leiomyosarcoma refractory to ifosfamide, doxorubicin and trabectedin, who experienced a sustained and progressive response to GCB alone.<br/><br/>Conclusions:  Gemcitabine also when given as a mono-chemotherapy can obtain a long lasting tumour control in heavy pre-treated patients with uterine LMS and should be considered as a possible option for this subset of patients.<br/>]]></description>
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<title><![CDATA[Potential contribution of aspirin to cancer control programmes]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.100</link>
<pubdate>Wed, 12 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Abstract<br/><br/>Chemoprevention describes the potential of chemicals to intervene and block multistage carcinogenesis.  Aspirin (acetylsalicylate) is showing cancer chemopreventive potential and the medicine has public health potential given that low-doses also reduce the risk of cardiovascular events by up to 30%.  Whilst recognising that aspirin has undesirable effects, perhaps the medicine may compliment other cancer control programmes such as screening and lifestyle measures.  Furthermore, perhaps the cancer chemopreventive potential of aspirin might be mediated, at least in part, by salicylate which is present in fruits and vegetables.  Salicylate might therefore be considered to be a nutraceutical.  Furthermore, there are a number of matters that arise including the potential for the public health field to further advocate the self-care preventive agenda, which might include aspirin.  Perhaps it is now timely for a conference on the public health potential of aspirin to be convened.<br/><br/>Key words : <br/>aspirin, cancer control, salicylate, nutraceutical, public health          <br/>]]></description>
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<title><![CDATA[Poorly differentiated synovial sarcoma of the vagina: A case report and a clinical literature review]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.99</link>
<pubdate>Wed, 19 Nov 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Synovial sarcomas (SS) account for 5 to 10 percent of soft-tissue sarcomas, and typically arise in the para-articular regions of adolescents and young adults. Nonetheless, SS can rarely occur in other regions of the body. Here we present a first clinical literature report of a patient with a SS arising from the vaginal wall. A 40 year-old patient who present a necrotic polypoid lesion measuring 50 mm and extending from the external urethral meatus to the middle part of the anterior vaginal wall. The Biopsy showed a poorly differentiated SS with abundant necrosis and a SYT-SSX1 mutation. Staging CT scan was negative for distant metastases.  The patient, prior to the radical surgery, received neoadjuvant chemotherapy (ifosfamide and epirubicin) for three cycles. She underwent post operative external and brachytherapy (50 Gy) due to close margins (< 1mm) on pathologic specimen. She relapsed eleven and sixteen months later with lung metastases which both times were successfully removed by surgical resection. At twenty-five months from diagnosis, the patient is alive without further evidence of disease. In summary, in the presence of unfavourable prognosis factors, the neoadjuvant chemotherapy could be the primary approach to reduce the tumor size and the risk of distant micro-metastases allowing a less aggressive radical surgery if tumor is located in non-extremity site. Multidisciplinary approach, if no influencing overall survival and disease free survival, may improve the quality of life. In fact in our patient we obtained a complete clinical control in the pelvis avoiding pelvic exenteration with neoadjuvant chemotherapy.]]></description>
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<title><![CDATA[Construction of knowledge and perception of mammography in the UK]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.98</link>
<pubdate>Tue, 30 Sep 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Objective: The benefit of mammography is overestimated among UK women although the National Health Service (NHS) offers comprehensive information about breast screening with its official pamphlet. This study examined how women in the UK construct their views of mammography and how they interpret the information of the NHS pamphlets and newspaper articles about breast screening.<br/><br/>Methods: Focus groups and individual interviews to 11 female participants aged 26-58 were conducted using a base-line questionnaire.<br/><br/>Result: Many participants possessed knowledge about mammography which was different from the facts of medical consensus. Various factors, including self beliefs, experience of breast cancer or being screened with a mammogram, and stories from friends and relatives, could influence intertwiningly on the participants view about breast screening with a mammogram. Skeptical attitudes towards the media description of breast screening issues were revealed. The participants felt that the NHS pamphlets offered enough information about breast screening.<br/><br/>Conclusion: The women in this study showed that people may not be surrounded by the practical information sources to know about mammogram efficacy until they are invited to the breast screening. In order to achieve democratic discussion over breast screening including mammography, the NHS and mass media have a room for further cooperation to provide the full picture of breast screening to the public. <br/>]]></description>
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<title><![CDATA[Intra-operative measurement of tumour size in breast cancer and its comparison with other methods: A prospective study]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.96</link>
<pubdate>Fri, 26 Sep 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Accurate measurement of breast tumor size determines staging and prognosis. Discrepancy amongst clinical examination (CE), ultrasonography (USG), mammography (MG), pathological examination (PE), and magnetic resonance imaging (MRI) has been reported.  But few studies have evaluated changes in breast tumor size from the operating table to the laboratory.<br/><br/>Objectives and Methods:  A prospective study was designed to assess the intra-operative (IO) tumor size in 29 patients of breast cancer presenting to a tertiary care center in Delhi, and to compare it with CE, USG, and PE. <br/><br/>Observations and Results: Twenty-nine patients (mean age: 47 years), presenting with invasive duct carcinoma (stage IIIA: 31%, stage IIB: 28%), were included in the study. Comparison with mean IO (4.2 cm) revealed that both USG and PE underestimated tumor size by a mean of 0.35 cm (8.4 %), and 0.45 cm (10.7%) respectively, in most patients. CE tended to overestimate size by 0.82 cm (19.8%). All 3 modalities showed statistically significant correlation with IO (maximum Pearsons correlation co-efficient for PE=0.937, p<0.001 R2 =0.877, maximum for PE). Two-way analysis of variance revealed mean difference in size to be statistically significant (p=0.000) only between CE and IO.  <br/><br/>Discussion: Formalin processing causes changes in tumor dimensions in the breast, causing reduction in tumor size. It may also have a bearing on the assessment of surgical margins in breast conservation surgery. Immediate postoperative measurement of the specimen is ideal. Protocol for specimen fixation should be standardized.<br/>]]></description>
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<title><![CDATA[Report of the Integrative Molecular Cancer Epidemiology International Symposium, Lyon, France]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.95</link>
<pubdate>Thu, 11 Sep 2008 00:00:00 GMT</pubdate>
<description><![CDATA[An international Symposium on Integrative Molecular Cancer Epidemiology took place in Lyon, France, on 3rd-5th July 2008. The Symposium focused on aetiologic and mechanistic aspects of molecular and genetic cancer epidemiology research and was divided into three following sections: 1) Molecular epidemiology - Application of novel molecular markers to cancer epidemiology 2) Genomic epidemiology in the era of whole genome scan 3) Integrative molecular epidemiology  Visions for the future. Participants included epidemiologists, geneticists, biochemical and molecular biologists, pharmacologists, pathologists and all researchers interested in this field. The Symposium was very useful to provide a complete and clear overview of the present and future of molecular cancer epidemiology. It was also useful both to encourage international scientific collaboration between investigators working in this specific research field, and to stimulate transdisciplinary research with experts of other research areas. Highlights of each of the scientific presentations are summarised below.<br/><br/><br/>]]></description>
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<title><![CDATA[Epithelial-myoepithelial parotid carcinoma after kidney transplantation]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.92</link>
<pubdate>Thu, 21 Aug 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The occurrence of a second malignant neoplasm (SMN) in patients who have been submitted to kidney transplantation is increasing and causes concern parotid carcinoma is rarely reported after transplantation and may be related to long-term chemotherapy.<br/><br/>Salivary gland carcinomas displaying exclusively myoepithelial differentiation- myoepithelial carcinoma (EMC) are rare, less than 1% of all salivary gland tumours. MEC arises most commonly in the parotid gland and usually occurs in women. The histopathologic features, immuno- histochemical profile, and clinical behaviour remains controversial.<br/>]]></description>
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<title><![CDATA[A phase II study of thalidomide and temozolomide in patients with brain metastases from malignant melanoma. Lymphopenia correlates with response]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.91</link>
<pubdate>Fri, 15 Aug 2008 00:00:00 GMT</pubdate>
<description><![CDATA[BACKGROUND: CNS metastases develop in nearly half of patients with advanced melanoma and in 15-20 % CNS is the first site of relapse. Median overall survival is short, ranging from 2 to 4 months, and 1-year survival is only 10 to 15 %. THA has been shown to have both antiangiogenetic and immunomodulating effects. TMZ is an oral alkylating agent with an excellent oral bio-availability and it is highly lipophilic with an ability to penetrate the blood-brain barrier. TMZ and THA in combination were tested in patients with brain metastases from malignant melanoma (MM).<br/><br/>METHODS: Between June 2004 and February 2007 patients with measurable metastatic melanoma in progression and PS < 1 received TMZ in a dose of 150 mg/m2 qd for 7 days, followed by 7 days off therapy and THA in 200 mg qd, both orally administered. Concomitant treatment with steroids was allowed. PBMCs were collected from the last 14 consecutive patients for evaluation of immune parameters. <br/><br/>RESULTS: 40 screened patients were eligible and evaluable for response and 39 were evaluable for toxicity. 25 patients had asymptomatic and 15 symptomatic brain metastases. The toxicity was primarily grade 1-2 with no grade 4 or treatment related deaths. Four patients had tromboembolic events grade 3. One pt obtained a CR and 5 PR in the CNS, while 2 had CR and 4 PR outside CNS. Overall response rate was 17.5%. We found a significant positive correlation between lymphopenia and objective response.<br/><br/>CONCLUSIONS: The combination treatment was well tolerated but with more frequent thromboembolic events compared to single drug TMZ or THA. The treatment demonstrated activity in CNS as well as outside CNS. The correlation between lymphopenia and objective response needs further investigation.]]></description>
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<title><![CDATA[Defeating cancer with antidepressants]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.88</link>
<pubdate>Thu, 21 Aug 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Prostaglandins are ephemeral, infinitesimal signalers self-regulating every cell in the body, including those subserving mood and immunity. At first they were perceived as a master switch, but now are believed to regulate every component of cellular microanatomy and physiology, including those of the organelles, cytoskeleton, proteins, enzymes, nucleic acids and mitochondria. Prostaglandins are responsible, paradoxically, for cell function and dysfunction. Excessive prostaglandin synthesis depresses immune function and may induce cancer. An ideal anticancer agent would inhibit prostaglandins in such a manner as to shut down the pathogenesis of cancer. In this article I will show that antidepressants have such properties.]]></description>
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<title><![CDATA[Report of the Second International Symposium on Molecular Epidemiology in Childhood Leukaemia and Embryonal Tumours, Rio de Janeiro, Brazil]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.86</link>
<pubdate>Thu, 5 Jun 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The recent International Symposium on Molecular-epidemiology in Embryonal tumours and paediatric leukaemia was held on March 4-6 2008 in Rio de Janeiro, Brazil. It was a very productive meeting in which studies relating to genetics and therapeutical trials, identification of risk factors in acute leukaemia neuroblastoma and Wilms tumours were presented. Over one hundred and twenty participants gathered for three days of fruitful discussions, including representatives of paediatrics, haematology, laboratory, epidemiology and pathology. Debates about strategies of applications of important biomarkers for clinical trials were discussed. Highlights of each of the scientific presentations are summarised below.]]></description>
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<title><![CDATA[Eurocan Plus Report: Feasibility Study for Coordination of National Cancer Research Activities]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.84</link>
<pubdate>Tue, 20 May 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The process that resulted in the submission and funding of the Eurocan+Plus Project by the 6th Framework Programme was initiated by the European Parliament.<br/><br/>This report summarises the key findings and conclusions of the Eurocan+Plus Project which ran between October 2005 and December 2007, and outlines proposals for action in the short and the longer term.<br/><br/>Participants in the Project represented themselves and not the institution where they work. The Project was in no way a formal collaboration between any governmental body, funding agency, research or medical institution of any of the 27 EU Member States. In this respect, proposals in this Summary Report and in other deliverables in no way represent a formal commitment ofany governmental or non-governmental institution for any idea proposed by the Project.<br/><br/>For more information on the topics developed in this report, interested readers are invited to consult the reports issued by the different Work Packages. These reports can be consulted on the Project website www.eurocanplus.eu.]]></description>
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<title><![CDATA[Syzygium cumini inhibits growth and induces apoptosis in cervical cancer cell lines: A primary study]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.83</link>
<pubdate>Thu, 21 Aug 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Cervical cancer is common among women in the Indian subcontinent and the incidences and death rates are gradually increasing over the years. Several dietary phytochemicals have been reported to have growth inhibitory and apoptotic effect on HeLa and other cervical cell lines. In this study, using Hoechst 33342 staining, MTT, Annexin V-FLUOS/PI  and TUNEL assays we demonstrated that Syzygium cumini extract inhibits the growth and induces apoptosis in HeLa and SiHa cervical cancer cell lines in a dose and time dependent manner. The phytochemical, its mode of action, and safety issues are yet to be determined.]]></description>
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<title><![CDATA[A Randomised Prospective Study of Extended Tocopherol and Pentoxifylline Therapy, in Addition to Carbogen, in the Treatment of Radiation Late Effects]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.81</link>
<pubdate>Mon, 9 Jun 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Purpose: Pentoxifylline (PTX) and tocopherol (Vitamin E) are antioxidants previously shown to be useful in combination in the treatment of late radiation induced toxicity. The purpose of this study was to investigate the benefit of combination therapy with carbogen pentoxifylline and tocopherol in the mitigation of late radiation effects. As the optimal duration of PTX and tocopherol treatment has not been fully established, we studied short versus extended treatment duration.   <br/> <br/>Methods: We conducted a phase II prospective randomised study of short versus prolonged treatment with pentoxifylline (800 mg) and tocopherol (1000 IU) orally once daily in patients with grade 3 toxicity post radical radiotherapy. In addition, all 18 patients received inhaled carbogen (95% oxygen + 5% CO2) over 90 minutes, 5 days per, week for 3 weeks. The primary endpoint was improvement in maximum Lent-Soma toxicity scores.<br/>	<br/>Results: Maximum Lent-Soma scores improved in six of the eighteen patients (response rate 33%). The proportion of patients responding to treatment in the prolonged treatment arm B was more than double than in the shorter arm A, but this did not reach statistical significance (p  0.321). Two patients who had prolonged treatment (arm B) had complete resolution of their symptoms which was maintained at 2 and 3 years follow up. <br/>           <br/>Conclusions: We recommend prolonged treatment for 12 months, with PTX and tocopherol in combination with carbogen therapy, in the management of late radiation effects.<br/>]]></description>
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<title><![CDATA[Changes in Cancer Incidence and Mortality in England & Wales and a comparison of cancer deaths in the Major Developed Countries by Age and Sex 1979-2002 in context of GDP Expenditure on Health]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.80</link>
<pubdate>Mon, 28 Jul 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background<br/>The successful treatment of cancer is a major health and political issue in England & Wales and also in the Major Developed Countries (MDC). All Malignancy deaths by age and gender are analysed to determine how successful the MDC were in reducing cancer deaths between 1979-2002 within the context of the each nations Gross-Domestic-Product-Expenditure-on-Health (GDPEH) over the period.<br/><br/>Method<br/>Incidence rates of new cancers in England & Wales are examined for 1979-80 to 2003-04 to highlight extent of the problem. Set in the context of GDREH for each MDC 1980-2002 as an indicator of how each nation has responded to the challenge of cancer. The changing cancer mortality rates for England & Wales are compared with each MDC by age and sex using WHO All Malignancies mortality rates over the period 1979-81 to 2000-02.  Chi square tests are used to compare outcomes between England & Wales with each MDC.<br/><br/>Results<br/>1] Mens All Age malignancy incidence in England & Wales rose 48% and womens 51% with notable rises for females aged 15-34 and 55-74years.<br/>2] Every MDC increased GDPEH substantially UK up to 9.3% but remains 8th of ten MDC and still below the MDC average (9.85%).<br/>3] England & Wales mens average (15-74years) deaths were 3rd highest in 1979-81 but fell to 8th by 2000-02 declining significantly more than 7 other MDC.<br/>England & Wales womens average (15-74 years) rates were highest in 1979-81 and in 2000-02 but declined significantly more than most MDC in every age band from 35-74 years.<br/>4] Most MDC countries mens rates declined significantly more than their womens except Japan and Spain but the improvements in mens cancer death were not matched in womens rates especially the 35-54s. <br/> Conclusions: Rising incidence poses problems for every MDC but especially for England & Wales as does the relatively low Anglo-Welsh GDPEH whilst poorer womens results should be a matter of concern for most MDC. The reductions in cancer deaths reflects well on all front-line services indicating what can be achieved with improved GDDPEH but should not obscure the challenge of the rising incidence of cancer.]]></description>
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<title><![CDATA[Efficacy of 90Y Ibritumomab-Tiuxetan Treatment in a Case of Resistant Gastric Malt Non Hodgkin's Lymphoma]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.79</link>
<pubdate>Thu, 13 Mar 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Treatment modalities for resistant/relapsing gastric mucosa associated lymphoid tissue (MALT) non Hodgkins Lymphoma (NHL) are not yet well standardized. In the past most patients were treated surgically with a gastrectomy while more recently radiotherapy (RT) and systemic approaches (chemotherapy and immunotherapy) have been used with improving results.<br/><br/>Here we report the case of a patient affected by MALT NHL resistant to antibiotics chemotherapy and immunotherapy who achieved a durable complete remission after radio-immunotherapy treatment with Zevalin (90Y ibritumomab-tiuxetan) administered in a single standard dose. This observation must be confirmed on a larger series but suggests that radio-immunotherapy may be a valid approach in treating MALT NHL patients relapsing or those resistant to conventional therapies so avoiding more aggressive and toxic approaches.<br/>]]></description>
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<title><![CDATA[Surgical 'damage control' treatment of a large retroperitoneal liposarcoma encasing a horse-shoe kidney]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.77</link>
<pubdate>Mon, 7 Jul 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Damage control is a surgical strategy for severely compromised trauma patients based on speed control of life-threatening injuries that aims to rapidly resuscitate patients in intensive care unit (ICU). We report about the use of such therapeutic strategy in a patient affected by a retroperitoneal sarcoma concomitant to a horse-shoe kidney, a relatively rare anatomical malformation.]]></description>
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<title><![CDATA[2007 EORTC-NCI-ASCO Annual Meeting:  Molecular Markers in Cancer]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.75</link>
<pubdate>Mon, 18 Feb 2008 00:00:00 GMT</pubdate>
<description><![CDATA[The recent EORTC-NCI-ASCO Annual Meeting on Molecular Markers in Cancer was held on November 15-17, 2007 in Brussels, Belgium.  It was the largest meeting to-date and marked the first year in which the American Association of Clinical Oncology (ASCO) joined in the efforts of the European Organisation for Research and Treatment of Cancer (EORTC) and the National Cancer Institute (NCI) in organizing this annual event. More than 300 clinicians, pathologists, laboratory scientists and representatives from regulatory agencies and the pharmaceutical industry came together for three days of intense discussion, debate and reflection on the latest biomarker therapeutic discoveries, strategies and clinical applications. The poster discussion sessions featured 79 research abstracts.  The three most outstanding abstracts, all authored by young female researchers, were selected for presentation during the main meeting sessions.  Highlights of each scientific session are presented.]]></description>
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<title><![CDATA[Management training for hospital administrators: Sentinel lymph-node biopsy under local anaesthetic for carcinoma of the breast - organisational and economic impact]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.74</link>
<pubdate>Fri, 15 Feb 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Sentinel lymph-node biopsy under local anaesthetic for carcinoma of the breast: organisational and economic impact.<br/><br/>This study compares sentinel lymph-node biopsy carried out at the time of removal of the primary breast tumour, under general anaesthetic, with sentinel lymph-node biopsy carried out under local anaesthetic prior to the main operation.<br/><br/>It compares the total cost of the two treatment approaches, in terms of average income and of their impact on the subsequent programming of operations and hence on waiting lists and income.]]></description>
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<title><![CDATA[The effect of transdermal estradiol or oral conjugated oestrogen and fenretinide versus placebo on haemostasis and cardiovascular risk biomarkers in a randomised breast cancer chemoprevention trial]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.67</link>
<pubdate>Wed, 6 Feb 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Introduction:<br/>We have previously reported the favourable effect of transdermal estradiol (E2), relative to oral conjugated equine oestrogen (CEE), on ultrasensitive C-reactive protein after 12 months of treatment in a retinoid-placebo controlled two-by-two randomised breast cancer prevention trial (ref). Here we investigate the changes in lipids and clotting profile in patients of the same trial. <br/><br/>Methods and Results: <br/>Recent postmenopausal women were randomised to either oral CEE 0.625 mg/d and placebo (n=55), CEE and fenretinide 200 mg/d (n=56), transdermal E2 50 g/d and placebo (n=59), or E2 and fenretinide 200 mg/d (n=56). Sequential medroxyprogesterone acetate 10 mg/d was given in each group. After 12 months there was a statistically significant effect of the route of administration of hormone replacement therapy (HRT) on fibrinogen levels the median percent change being -5.7% with CEE and -1.1% with E2 (P=0.012). Total cholesterol decreased in all arms (P<0.0001). HDL-C decreased significantly with transdermal E2 (P=0.006) compared to oral CEE and with fenretinide relative to placebo (P<0.001). Triglycerides exhibited an opposite modulation by HRT route, with a 21.4% median increase with oral CEE and an 8.6% reduction with transdermal E2 (P<0.0001). Antithrombin-III showed a 4% borderline significant reduction in the fenretinide arm relative to placebo, irrespective of HRT administration route (P=0.055). <br/><br/>Conclusions:<br/>Our data indicate that transdermal E2 may be preferable to oral CEE based on its safer cardiovascular risk profile. Fenretinide modified some cardiovascular risk biomarkers and confirmed a safer profile compared to other retinoids.]]></description>
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<title><![CDATA[Post-genomic clinical trials - the perspective of ACGT]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.66</link>
<pubdate>Mon, 21 Jan 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Advancing Clinico Genomic Trials (ACGT) is an EU co-funded project that develops open-source semantic and grid-based technologies in support of post genomic clinical trials in cancer research. It addresses clinicians bio-researchers as well as software developers providing an open platform where novel and powerful services can be offered and put to use by practitioners in the field.<br/><br/>This article discusses the ACGT's approach to collecting and dealing with genomic data. It also looks at the ACGT's ultimate objective providing a unified technological infrastructure which will facilitate the seamless and secure access and analysis of multi-level clinical and genomic data enriched with high-performing knowledge discovery operations and services. <br/><br/>By doing so it is expected that the influence of genetic variation in oncogenesis will be revealed the molecular classification of cancer and the development of individualised therapies will be promoted and finally the in-silico tumour growth and therapy response will be realistically and reliably modelled.]]></description>
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<title><![CDATA[Full dose intraoperative radiotherapy with electrons (ELIOT) during breast conserving surgery: Experience with 1246 cases]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.65</link>
<pubdate>Tue, 26 Feb 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Abstract<br/>Background. Previous studies showed that after breast conserving surgery for breast cancer , Radiotherapy may be applied to the portion of the breast where the primary tumor was removed (partial breast irradiation - PBI) avoiding the irradiation of the whole breast. We developed a procedure of PBI consisting in a single high dose of radiotherapy of 21Gy with electrons equivalent to 58-60Gy in fractionated doses, delivered during the surgical session by a mobile linear accelerator, positioned close to the operating bed.<br/>Patients and methods From July 1999 to December 2006, 1246 patients with primary carcinoma less than 2.5 cm in diameter mostly over 48 years were treated with Electron IntraOperative Radiotherapy (ELIOT) at a single dose of 21Gy.<br/>Results. After a follow-up from 0.3 to 94.7 months (median 26), 24 patients (1.9 %) showed a local recurrence and 22 developed distant metastases. 16 patients died, 7 for breast carcinoma and 9 for others causes. The 5 years crude survival was 96.5%. Six cases (0.5%) developed serious breast fibrosis which resolved in two-three years. Other 40 patients suffered for mild fibrosis. Cosmetic results were good.<br/>Conclusions. ELIOT is a safe method for treating conservatively operated breasts, avoids the long period of postoperative radiotherapy greatly improving the quality of life and reduces the cost of Radiotherapy. ELIOT reduces radiation to normal surrounding tissues and deep organs. Results on short-term and middle-term toxicity are good. Data on local control are encouraging.]]></description>
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<title><![CDATA[Institutional guidelines and ongoing studies in management of liver tumours: The experience of the European Institute of Oncology]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.64</link>
<pubdate>Fri, 2 May 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background:<br/>An institutional task force on Upper Gastrointestinal Tumours is active at the European Institute of Oncology (EIO). Members decided to collect in a document the institutional guidelines on management of liver tumours (primary and metastatic). This article is aimed at presenting the current treatment guidelines as well as ongoing research protocols and trials in this field at EIO.<br/><br/>Methods:<br/>A steering committee convened to assign tasks to individual members. Contributions from experts in each treatment area were collected in a single document, in order to produce a draft for subsequent review from the aforementioned committee. Six drafts have been discussed and the final version approved.<br/><br/>Results:<br/>Surgical, Medical Oncology, Interventional Radiology, Nuclear Medicine and Radiation Therapy approaches, their roles in management of liver tumours and ongoing research trials are presented and discussed in this article.<br/><br/>Conclusions:<br/>At the European Institute of Oncology a multi-disciplinary integrated approach to liver tumours is a standard and several research ongoing projects are currently active in this field.]]></description>
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<title><![CDATA[Impact of a reduced dose intensity of adjuvant anthracycline based chemotherapy in a population-based cohort of stage I-II breast cancers]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2008.63</link>
<pubdate>Tue, 8 Jul 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Background: Reductions in the dose intensity (DI) of adjuvant anthracycline based chemotherapy in early stage breast cancer are frequently required due to treatment toxicity or poor tolerance, but the implications of a minimal reduction in DI on clinical outcome remain uncertain. <br/><br/>Patients and methods: Women with stage I-II breast cancer treated with adjuvant adriamycin and cyclophosphamide (AC) from 1990-1995 were identified in a provincial breast cancer database. Cases were classified into 4 cohorts 1: all cycles delivered at full dose and on time 2: one single dose reduction or dose delay 3: >1 dose reduction or dose delay 4: <2 cycles of chemotherapy delivered. <br/><br/>Results: 484 eligible cases were identified (cohort 1: n = 268 2: n= 88 3: n= 89 4: n= 39). Slight imbalances in lymph node status (p=0.05) and adjuvant hormonal therapy (p=0.05) were observed between the cohorts. 55% (267/484) of the patients had node-positive disease and 33% (158/484) were ER+. 45% of cases had a reduction in DI. With a median follow-up of 9.6 years, there were no significant differences in relapse-free survival (p=0.94), breast cancer-specific survival (p=0.87) or overall survival (p=0.86) between the 4 cohorts. Outcomes were independent of hormone receptor status.<br/><br/>Conclusions: Although toxicity related reductions in the DI of adjuvant AC chemotherapy for early stage breast cancer are common, they did not appear to significantly impact on clinical outcomes in this population-based cohort of women with stage I-II breast cancers. <br/>]]></description>
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<title><![CDATA[Does LigaSure(TM) reduce fluid drainage in axillary dissection? A randomised prospective clinical trial]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/eCMS.2007.61</link>
<pubdate>Thu, 29 Nov 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Background  Axillary lymph node dissection (ALND) is an integral part of breast cancer treatment. It is required in about 60% of patients. The placement of a drain in the axilla after an operation is current surgical practice. Short surgical stay programs increase operating efficiency and reduce medical care costs, without compromising quality of care. LigaSureTM is a new haemostatic device that  uses bipolar energy to seal vessels. The aim of this study was to determine whether axillary dissection with LigaSureTM reduces  the time of wound drainage, the duration of surgical intervention and the volume of drainage after treatment. <br/>Patients and Methods  This study is a prospective randomized controlled trial. 100 women with breast cancer who needed axillary dissection were randomized into the LigaSureTM or conventional axillary dissection group. Level I to III lymph node dissection was performed. A closed suction drain was always placed in the axilla and removed after 6-8 days or when fluid amount was < 60 cc in the previous 24 hours.<br/>Results  There were no significant differences between the two groups when considering the duration of surgical procedure: average duration was 70.7  24.66 minutes for LigaSureTM patients, while in the conventional dissection group the mean was 70.6  22.47 minutes (p=0.98). Total amount of drained fluid was 624.49 cc in the LigaSureTM axillary dissection group and 792.96 in the conventional ALND group; this difference did not achieve statistical significance (p=0.09);  the duration of draining was also similar with no statistical difference (p=0.15).<br/>Conclusions  The present study did not show clear advantages in LigaSureTM use for ALND, although it represents a good haemostatic device, especially in abdominal surgery.<br/><br/>Keywords  breast carcinoma; breast cancer surgery; axillary dissection; seroma; drain; haemostasis; LigaSure.]]></description>
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<title><![CDATA[Technique of sentinel lymph node biopsy and lymphatic mapping during laparoscopic colon resection for cancer]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.60</link>
<pubdate>Thu, 15 Nov 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Background: The utility of lymphnode mapping to improve staging in colon cancer is still under evaluation. Laparoscopic colectomy for colon cancer has been validated in multicentric trials. This study assessed the feasibility and technical aspects of lymphnode mapping in laparoscopic colectomy for colon cancer. Methods. Forty-two patients with histologically proven colon cancer were studied from January 2006 to September 2007. Exclusion criteria were: advanced disease (clinical stage III), rectal cancer, previous colon resection and contraindication to laparoscopy. Lymphnodal status was assessed preoperatively by computed tomography (CT) scan and intraoperatively with the aid of laparoscopic ultrasound. Before resection, 2-3 ml of Patent Blue V dye was injected subserosally around the tumor. Colored lymphnodes were marked as sentinel (SN) with metal clips or suture and laparoscopic colectomy with lymphadenectomy completed as normal. In case of failure of the intraoperative procedure an ex vivo SN biopsy was performed on the colectomy specimen after resection. Results. A total number of 904 lymphnodes were examined, with a median number of 22 lymphnodes harvested per patient. The SN detection rate was 100%, an ex vivo lymphnode mapping was necessary in 4 patients. Eleven (26.2%) patients had lymphnodal metastases and in 5 (45.5%) of these patients, SN was the only positive lymphnode. There were two (18.2%) false negative SN. In three cases (7.1%) with aberrant lymphatic drainage, lymphadenectomy was extended. The accuracy of SN mapping was 95.2% and negative predictive value was 93.9%. Conclusions: Laparoscopic lymphatic mapping and SN removal is feasible in laparoscopic colectomy for colon cancer. The ex vivo technique is useful as salvage technique in case of failure of the intraoperative procedure. Prospective studies are justified to determine the real accuracy and false negative rate of the technique.]]></description>
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<title><![CDATA[Response to neo-adjuvant chemotherapy for colorectal cancer liver metastases: A key for improving survival?]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.58</link>
<pubdate>Tue, 16 Oct 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Hepatic resection in metastatic disease from colorectal cancer offers the best chance in selected cases for long-term survival. Neoadjuvant chemotherapy (NACT) has been advocated in some cases initially deemed irresectable, with few reports of the efficacy of such a strategy and the influence of the response to chemotherapy on the outcome of radical hepatic resection. Methodology: Between December 1995 and May 2005, 27 patients with colorectal liver metastases, (7 males, 20 females, mean age: 58�� 8 years; range: 40-75) were treated with neoadjuvant chemotherapy. A 7 year survival analysis was performed. Chemotherapy included mainly 5-fluorouracil, leucovorin and either oxaliplatin or irinotecan for a median of 8 courses. <br/><br/>Sixteen patients (59%) had synchronous and 11 (41%) metachronous metastases. During pre-operative chemotherapy tumour regression occurred in 10 cases (37%); stable disease (SD) in a further 10 patients (37%) and progressive disease (PD) developed in 7 cases (26%). The 5 year overall survival for NACT responders was 64% and only 15% for non-responders (p=0.044).<br/><br/>The response to chemotherapy is likely to be a significant prognostic factor affecting survival after liver resection for cure.]]></description>
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<title><![CDATA[Elevated breast cancer risk among mothers of a population-based series of 2668 children with cancer]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.57</link>
<pubdate>Thu, 17 Jan 2008 00:00:00 GMT</pubdate>
<description><![CDATA[Aims: Although a previous study found high risk of breast cancer in mothers of children with soft tissue sarcomas, breast cancer risks in mothers of other childhood cancer largely remain unknown. The etiology is not fully understood. The present study explored this excess by varying type of childhood solid cancer and formulated a hypothesis.<br/><br/>Methods: Mothers of 2668 children with solid tumours included in the Manchester Childrens Tumour Registry, 1954-1996 were traced and followed up to 31st December 2000 through the UK National Health Service Central Register. Standardised Incidence Ratio(SIR), P-values and 95% confidence intervals were calculated from age and calendar year-specific female breast cancer incidence rates for England and Wales.<br/><br/>Results: There was a significant excess of breast cancer in mothers overall(SIR=1.3,95%CI=1.0-1.5) mainly due to mothers of children with rhabdomyosarcoma (RMS) (SIR=2.2, 95%CI=1.0-4.0), skin cancer(SIR=7.9, 95%CI=2.9-17.1), and central nervous system tumours(SIR=1.2, 95%CI=0.9-1.8). Maternal breast cancer risk was associated with late age at birth of the index child and male sex and young age at diagnosis in the index child. Risk was highest in the 10 years following the birth of the index. The pattern was seen most strongly in mothers of children with embryonal RMS.<br/><br/>Conclusion: There are excesses of breast cancer in mothers of children with solid tumours in general and specifically in RMS, skin and CNS. There appears to be a temporal relationship between certain tumours in children and breast cancer in their mothers, suggesting a origin of their respective pregnancy. We propose a mother-fetal<br/>interaction mechanism to explain this association.]]></description>
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<title><![CDATA[Developing a european grid infrastructure for cancer research: vision, architecture, and services]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecms.2007.56</link>
<pubdate>Fri, 21 Sep 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Life sciences are currently at the centre of an informational revolution. The nature and amount of information now available open directions of research that were once in the realm of science fiction. During this informational revolution, the data gathering capabilities have greatly surpassed the data analysis techniques. Data integration across heterogeneous data sources and data aggregation across different aspects of the biomedical spectrum, therefore, is at the centre of current biomedical and pharmaceutical R&D.<br/><br/>This paper reports on original results of the ACGT integrated project focusing on the design and development of a European Biomedical Grid infrastructure in support of multicentric, post genomic clinical trials on Cancer. Post-Genomic clinical trials (CTs) use multilevel clinical and genomic data and advanced computational analysis and visualization tools to test hypothesis in trying to identify the molecular reasons for a disease and the stratification of patients in terms of treatment. <br/><br/>The paper provides a presentation of the needs of users involved in post-genomic CTs, and presents indicative scenarios which drive the requirements of the engineering phase of the project. Subsequently, the initial architecture specified by the project is presented and its services are classified and discussed.  A range of such key services, including the Master Ontology on Cancer which lies at the heart of the integration architecture of the project, are presented. Special efforts have been taken to describe the methodological and technological framework of the project, enabling the creation of a legally compliant and trustful infrastructure.  <br/><br/>Finally, a short discussion of the forthcoming work is included and the potential involvement of the cancer research community in further development or utilization of the infrastructure is described.]]></description>
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<title><![CDATA[Robotic modified radical hysterectomy with pelvic lymphadenectomy]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.55</link>
<pubdate>Thu, 20 Sep 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Radical hysterectomy, the complete removal of a woman's uterus, is usually performed via an abdominal incision that requires a 3 to 5 day hospital stay and a 6 to 8 week recovery period. Now, in a handful of hospitals around the world, new robotic technology allows doctors to perform this procedure through small incisions that require a recovery time of only one night in the hospital and a significantly shorter recovery period at home. Watch such a procedure being carried out at the European Institute of Oncology.]]></description>
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<title><![CDATA[Policy Challenges for Cancer Research: A Call to Arms]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecancer.2008.53</link>
<pubdate>Tue, 18 Sep 2007 00:00:00 GMT</pubdate>
<description><![CDATA[Research has delivered remarkable benefits for cancer patients and their families since James Watson and Francis Crick wrote the now immortal line, "We wish to propose a structure for the salt of deoxyribonucleic acid" thus setting the molecular foundations for the modern era of cancer control.  The pace of technological innovation from fundamental scientific discoveries to the policy impact of huge population studies has been breathtaking. One has only to contrast a paper on the treatment of solid epithelial cancers written by Henri Tagnon and colleagues in 1966  with the myriad of chemotherapeutic approaches at the oncologists disposal today. Inevitably, as the tide of research has risen so it has bought the flotsam and jetsam of regulations and policies. Some have been helpful, many pointless and too many actually harmful. Naturally some of these regulatory and general policies (by this I mean those concerned with funding, structure and organisation) have been specifically targeted at cancer research, e.g. US National Cancer Act 1971, whilst others have been a product of the general regulatory environment with indirect consequences for cancer research, e.g. EU Data Protection Directive 1995. Policy issues thus cover a vast terrain criss-crossed by complex interdependencies between scientific areas, countries S&T policies and socio-political constructs. Unfortunately there has been little attention paid to the consequences of these policy issues from which the research community has, by and large, been passenger rather than driver.]]></description>
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<title><![CDATA[[18F] FDG uptake: pay attention to candies]]></title>
<link>http://www.ecancermedicalscience.com/view-article.asp?type=abstract&amp;doi=10.3332/ecms.2007.48</link>
<pubdate>Wed, 15 Aug 2007 00:00:00 GMT</pubdate>
<description><![CDATA[[18F]Fluorodeoxyglucose ([18F]FDG) is a positron emission radiotracer whose biodistribution is similar to glucose. The similar biodistribution of [18F]FDG and glucose in the human body requires a the fasting condition of at least 6 hours prior to performing a [18F]FDG Positron Emission Tomography ([18F]FDG PET) study.<br/><br/>In human studies, FDG PET images, in either the fasting state or the glucose-loaded state, have demonstrated that [18F]FDG uptake is decreased,in the tumour, and thus the PET image quality is impaired when plasma glucose levels are increased. All these results suggest that patients should fast before FDG PET studies and their plasma glucose concentration needs to be considered when assessing tumour glucose metabolism. For lymphomatous disease, the data  are contradictory and there are reports that insulin does not induce major changes in glucose uptake of lymphomatous tissue.<br/><br/>Here we report two cases of lymphoma in which [18F]FDG PET/Computed Tomography ([18F]FDG PET/CT) was used for chemotherapy response evaluation. in both cases initial [18F]FDG PET/CT scans were negative for neoplastic lesions but showed increased and diffuse FDG uptake in muscles. This led us to investigate better the importance of a fasting condition. A second [18F]FDG PET/CT performed 3-4 days later revealed pathological uptake in the lymphomatous lesions in both cases.<br/><br/>We demonstrate the importance of a euglycemic state  before [18F]FDG administration, and that a fasting period of at least 6 hours is required prior to administration.]]></description>
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