http://m.prnewswire.com/news-releases/oncolytics-biotech-inc-completes-patient-enrollment-in-uk-phase-i-clinical-trial-investigating-reolysin-in-combination-with-cyclophosphamide-in-patients-with-advanced-malignances-166384116.html

Oncolytics Biotech® Inc. Completes Patient Enrollment in U.K. Phase I Clinical Trial Investigating REOLYSIN® in Combination with Cyclophosphamide in Patients with Advanced Malignances

CALGARY, Aug. 16, 2012 /PRNewswire/ - Oncolytics Biotech Inc. ("Oncolytics") (TSX:ONC) (NASDAQ:ONCY) today announced that it has completed patient enrollment in its U.K. Phase I clinical trial using intravenously-administered REOLYSIN in combination with cyclophosphamide in patients with advanced malignancies (REO 012).

"We are pleased to complete enrollment of this technical study examining cyclophosphamide's potential to modulate the immune system's response to REOLYSIN," said Dr. Matt Coffey, COO of Oncolytics. "Studies of this type help to advance our understanding of the interaction between the immune system and our product."

The primary objective of the open label, dose-escalating, non-randomized, 36-patient study is to determine the Minimum Effective Immunomodulatory Dose (MED) of cyclophosphamide necessary to obtain successful immune modulation. Secondary objectives of the trial include assessing the safety profile of the combination and gathering any evidence of antitumor activity.

Eligible patients include those who have been diagnosed with advanced or metastatic solid tumors, including pancreatic, lung and ovarian cancers that are refractory to standard therapy, or for which no standard curative therapy exists.

The principal investigators for the study are Dr. James Spicer of King's College, London, Dr. Johann de Bono and Dr. Kevin Harrington of the Royal Marsden NHS Foundation Trust and the Institute of Cancer Research, London, and Professor Hardev Pandha of the Royal Surrey County Hospital NHS Trust, Surrey and Mount Alvernia Hospitals.

About Oncolytics Biotech Inc.

Oncolytics is a Calgary-based biotechnology company focused on the development of oncolytic viruses as potential cancer therapeutics. Oncolytics' clinical program includes a variety of human trials including a Phase III trial in head and neck cancers using REOLYSIN, its proprietary formulation of the human reovirus. For further information about Oncolytics, please visit: www.oncolyticsbiotech.com.

This press release contains forward-looking statements, within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements, including the Company's expectations related to the U.K. Phase I clinical trial with REOLYSIN in combination with cyclophosphamide , and the Company's belief as to the potential of REOLYSIN as a cancer therapeutic, involve known and unknown risks and uncertainties, which could cause the Company's actual results to differ materially from those in the forward-looking statements. Such risks and uncertainties include, among others, the availability of funds and resources to pursue research and development projects, the efficacy of REOLYSIN as a cancer treatment, the tolerability of REOLYSIN outside a controlled test, the success and timely completion of clinical studies and trials, the Company's ability to successfully commercialize REOLYSIN, uncertainties related to the research and development of pharmaceuticals and uncertainties related to the regulatory process. Investors should consult the Company's quarterly and annual filings with the Canadian and U.S. securities commissions for additional information on risks and uncertainties relating to the forward-looking statements. Investors are cautioned against placing undue reliance on forward-looking statements. The Company does not undertake to update these forward-looking statements, except as required by applicable laws.

SOURCE Oncolytics Biotech Inc.

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Universal health coverage achieved by Mexico in less than a decade

Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?

Increased incidence of brain metastases in BRCA1-related ovarian cancers.

http://www.ncbi.nlm.nih.gov/m/pubmed/22889437/?i=5&from=ovarian%20cancer

Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.

http://www.ncbi.nlm.nih.gov/m/pubmed/22890887/?i=3&from=ovarian%20cancer

Kramer explains results of the PLCO trial « NCI Benchmarks

http://benchmarks.cancer.gov/2012/08/kramer-explains-results-of-the-plco-trial/

Delays Plague Breast and Ovarian Cancer Research – The Jewish Daily Forward

-research

Launching a 'social networking war' against cancer

http://medicalxpress.com/news/2012-08-social-networking-war-cancer.html

Pre-test genetic counseling increases cancer knowledge for BRCA patients - podcast

http://m.medicalxpress.com/news/2012-08-pre-test-genetic-cancer-knowledge-brca.html

CCR: Pre-invasive ovarian mucinous tumors are characterized by CDKN2A and RAS pathway aberrations.

http://m.clincancerres.aacrjournals.org/content/early/2012/08/11/1078-0432.CCR-12-1103


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Health News - Mechanisms of Acquired Chemoresistance in Ovarian Cancer Identified

-Ovarian-Cancer-Identified.html?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+healthnewshc%2FOxfp+%28Health+News+from+HealthCanal.com%29&utm_content=Google+Reader

JTM | open access | Correlation of pretreatment drug induced apoptosis in ovarian cancer cells with patient survival and clinical response (MiCK assay)

JTM | Abstract | Correlation of pretreatment drug induced apoptosis in ovarian cancer cells with patient survival and clinical response

Conclusion

The MiCK assay can predict the chemotherapy associated with better outcomes in ovarian cancer patients. This study quantifies outcome benefits on which a prospective randomized trial can be developed.

BMC Palliative Care | Full text | A national study of chaplaincy services and end-of-life outcomes

BMC Palliative Care | Full text | A national study of chaplaincy services and end-of-life outcomes

open access: Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer

Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer

Olanzapine for the Relief of Nausea in Patients With Advanced Cancer and Incomplete Bowel Obstruction | DocGuide

Olanzapine for the Relief of Nausea in Patients With Advanced Cancer and Incomplete Bowel Obstruction | DocGuide

Cancer Australia Connect - July 2012 issue (includes resources, guidelines....)

Untitled Document

doc2doc forum: Why are 25% of deaths not being properly recorded?

http://tinyurl.com/dxg6gvn

Forums  »  Open clinical  »  General clinical  »  Why are 25% of deaths not being properly recorded?

Taking Action Health Equity in Canada - Canadian Doctors for Medicare

TakingActionHealthEquity

Incidence and predictors of venous thromboembolism (VTE) among ambulatory high-risk cancer patients undergoing chemotherapy in the United States - Khorana - 2012 - Cancer - Wiley Online Library

Abstract

BACKGROUND:

Recent studies suggest that thromboprophylaxis is beneficial in preventing venous thromboembolism (VTE) in cancer outpatients, but this is not widely adopted because of incomplete understanding of the contemporary incidence of VTE and concerns about bleeding. Therefore, the authors examined the incidence and predictors of VTE in ambulatory patients with bladder, colorectal, lung, ovary, pancreas, or gastric cancers.

METHODS:

Data were extracted from a large health care claims database of commercially insured patients in the United States between 2004 and 2009. Demographic and clinical characteristics of the cancer cohort (N = 17,284) and an age/sex-matched, noncancer control cohort were evaluated. VTE incidence was recorded during a 3-month to 12-month follow-up period after the initiation of chemotherapy. Multivariate analyses were conducted to identify independent predictors of VTE and bleeding.

RESULTS:

The mean age of the study population was 64 years, and 51% of patients were women. VTE occurred in 12.6% of the cancer cohort (n = 2170) over 12 months after the initiation of chemotherapy versus 1.4% of controls (n = 237; P < .0001); incidence ranged by cancer type from 19.2% (pancreatic cancer) to 8.2% (bladder cancer). Predictors of VTE included type of cancer, comorbidities (Charlson Comorbidity Index score or obesity), and commonly used specific antineoplastic or supportive care agents (cisplatin, bevacizumab, and erythropoietin).

CONCLUSIONS:

This large, contemporary, real-world analysis confirmed high rates of VTE in select patients with solid tumors and suggested that the incidence of VTE is high in the real-world setting. Awareness of the benefits of targeted thromboprophylaxis may result in a clinically significant reduction in the burden of VTE in this population. Cancer 2012. © 2012 American Cancer Society.

http://onlinelibrary.wiley.com/doi/10.1002/cncr.27772/abstract;jsessionid=48B8081B141F0857048BECC4CDB4F41D.d04t01

All-cause mortality and cancer incidence

http://www.ncbi.nlm.nih.gov/m/pubmed/22886909/

Roche’s Avastin may receive ovarian cancer recommendation from NICE if lower than approved dose is considered - FT.com

ADzHH

Social media in healthcare- a BMC Medicine twitter chat now on Storify!

Social media in healthcare- a BMC Medicine twitter chat now on Storify!

Following the publication of 'Medicine, morality and health care social media' in BMC Medicine, author Farris Timimi (Medical Director, Mayo Clinic Center for Social Media, @FarrisTimimi) and his colleague Lee Aase (Director, Mayo Clinic Center for Social Media, @LeeAase) joined BMC Medicine Editor Sabina Alam (@BMCMedicine) in a twitter chat to discuss the ideas raised in Timimi's commentary.

It was apparent there was consensus amongst the contributors of the twitter chat – social media should be used as a tool by healthcare providers to interact with patients. Some systems are already in place, but more work is required to develop the right kind of social media platforms, and perhaps more importantly, more physicians should be encouraged to learn how to use social media to engage with the general public. Whether the medical institutions should make this a requirement remains to be determined.

A summary of the discussion with a selection of the contributions can be viewed at Storify.

Following the success of this chat we are considering having more in the future. If you feel there are any topics that should be discussed please get in touch via email, or of course tweet at us ! (@BMCMedicine)

Patients with Lynch Syndrome Mismatch Repair Gene Mutations Are at Higher Risk for Not Only Upper Tract Urothelial Cancer but Also Bladder Cancer.

Patients with Lynch Syndrome Mismatch Repair Gene Mutations Are at Higher Risk for Not Only Upper Tract Urothelial Cancer but Also Bladder Cancer.

Patients with Lynch Syndrome Mismatch Repair Gene Mutations Are at Higher Risk for Not Only Upper Tract Urothelial Cancer but Also Bladder Cancer.

Eur Urol. 2012 Aug 2;

Authors: Skeldon SC, Semotiuk K, Aronson M, Holter S, Gallinger S, Pollett A, Kuk C, van Rhijn B, Bostrom P, Cohen Z, Fleshner NE, Jewett MA, Hanna S, Shariat SF, Van Der Kwast TH, Evans A, Catto J, Bapat B, Zlotta AR

Abstract

BACKGROUND: Lynch syndrome (LS), or hereditary nonpolyposis colorectal cancer, is caused by mutations in mismatch repair (MMR) genes. An increased risk for upper tract urothelial carcinoma (UTUC) has been described in this population; however, data regarding the risk for bladder cancer (BCa) are sparse. OBJECTIVE: To assess the risk of BCa in MMR mutation carriers and suggest screening and management recommendations. DESIGN, SETTING, AND PARTICIPANTS: Cancer data from 1980 to 2007 were obtained from the Familial Gastrointestinal Cancer Registry in Toronto for 321 persons with known MMR mutations: mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) (MLH1); mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) (MSH2); mutS homolog 6 (E. coli) (MSH6); and PMS2 postmeiotic segregation increased 2 (S. cerevisiae) (PMS2). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Standardized incidence ratios from the Ontario Cancer Registry, using the Surveillance Epidemiology and End Results public database, were used to compare cancer risk in patients with MMR mutations with the Canadian population. Microsatellite instability analysis and immunohistochemistry (IHC) of the MMR proteins were also performed and the results compared with matched sporadic bladder tumors. RESULTS AND LIMITATIONS: Eleven of 177 patients with MSH2 mutations (6.21%, p<0.001 compared with the Canadian population) were found to have BCa, compared with 3 of 129 patients with MLH1 mutations (2.32%, p>0.05). Of these 11 tumors, 81.8% lacked expression of MSH2 on IHC, compared with the matched sporadic cases, which all displayed normal expression of MSH2 and MLH1. The incidence of UTUC among MSH2 carriers was 3.95% (p<0.001), and all tumors were found to be deficient in MSH2 expression on IHC. Mutations in the intron 5 splice site and exon 7 of the MSH2 gene increased the risk of urothelial cancer. Limitations include possible inflated risk estimates due to ascertainment bias. CONCLUSIONS: LS patients with MSH2 mutations are at an increased risk for not only UTUC but also BCa and could be offered appropriate screening.

PMID: 22883484 [PubMed - as supplied by publisher]

[Ovarian cancer--modern approach to its origin and histogenesis].

[Ovarian cancer--modern approach to its origin and histogenesis].

[Ovarian cancer--modern approach to its origin and histogenesis].

Abstract

Ovarian cancers (OC) belong to a heterogeneous group of pathologies and are traditionally classified with regard to histological type and degree of differentiation. OC was hypothesized to originate from ovarian surface epithelium (OSE) and inclusion cysts epithelium (IC). Unfortunately this theory was never supported by any clinical or molecular evidence linking carcinogenesis with OSE and was refuted. OC subtypes demonstrate morphologic features that resemble Müllerian duct-derived epithelia of the genital tract. Investigations of the HOX gene family Müllerian epithelial differentiation markers, confirmed the HOX genes expression in many subtypes of OC but not in OSE. The first step towards connecting OC origin with other than OSE genital tract structures were epidemiological observations indicating a minor OC risk after tubal ligation in women with the BRCA mutation. The first in situ carcinoma was found in the Fallopian tube fimbriae. Further research confirmed the same mechanism in sporadic OC. Endometriosis and endometrium cells may be a highly probable place of endometrioid OC initiation. Mucinous types share common futures with gastrointestinal tract cancers and there one needs to search for their precursors. Clear cell carcinoma may arise from glandular epithelium of endocervix or from endometrioid foci. The new classification of OC was proposed in 2004, suggesting to divide all OC into two types: I and II. Type II includes serous and endometrioid G3 subtypes, carcinosarcomas and undifferentiated OC. They are responsible for 75% of OC morbidity identified usually in FIGO stages Ill or IV, have poor prognosis and relapse early The remaining hystiotypes, with better prognosis and earlier FIGO stages at time of diagnosis, were classified as type I. Serous and endometrioid poorly differentiated ovarian cancers demonstrate mutation in TP53 gene (type II) and highly differentiated ones, generally in BRAS and KRAS genes (type I). The differences in molecular pathways also confirm different patterns of carcinogenesis of both OC types. Modern approach to OC histogenesis and origin emphasizes the necessity to verify OC screening, detection and treatment methods.

PMID: 22880466 [PubMed - in process]

Clear Cell Carcinoma of the Female Genital Tract (Not Everything Is as Clear as it Seems).

Clear Cell Carcinoma of the Female Genital Tract (Not Everything Is as Clear as it Seems).

Clear Cell Carcinoma of the Female Genital Tract (Not Everything Is as Clear as it Seems).

Adv Anat Pathol. 2012 Sep;19(5):296-312

Abstract

Clear cell carcinoma has a storied history in the female genital tract. From the initial designation of ovarian clear cell adenocarcinoma as "mesonephroma" to the linkage between vaginal clear cell carcinoma and diethylstilbestrol exposure in utero, gynecologic tract clear cell tumors have puzzled investigators, posed therapeutic dilemmas for oncologists, and otherwise presented major differential diagnostic challenges for pathologists. One of the most common errors in gynecologic pathology is misdiagnosis of clear cell carcinoma, on both frozen section and permanent section. Given the poor response to platinum-based chemotherapy for advanced-stage disease and increased risk of thromboembolism, accurate diagnosis of clear cell carcinoma is important in the female genital tract. This review (1) presents the clinical and pathologic features of female genital tract clear cell carcinomas; (2) highlights recent molecular developments; (3) identifies areas of potential diagnostic confusion; and (4) presents solutions for these diagnostic problems where they exist.

PMID: 22885379 [PubMed 

Beyond Office Hours: New App, Patient Portal, to Allow U-M Patients Mobile Access to Health Records

http://www.newswise.com/articles/view/592545/?sc=rsla&utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+NewswiseLatestNews+%28Newswise%3A+Latest+News%29&utm_content=Google+Reader

Empathy in Healthcare's a Waste, Unless It's a Strategic Focus - Forbes

nless-its-a-strategic-focus/

Quality of Life in Patients after Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy: Is It Worth the Risk?

Quality of Life in Patients after Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy: Is It Worth the Risk?

Abstract

Objective  

To investigate the course of health-related quality of life (HQL) over time in patients with peritoneal carcinomatosis (PC)
after complete cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).

Methods  

Prospective, single-center, nonrandomized cohort study using the European Organization for Research and Treatment of Cancer
Quality of Life Questionnaire.

Results  

Ninety patients who underwent CRS and HIPEC for PC in our institution were enrolled in the study. Mean age was 56 years (range
27–77 years) (61 % female). Primary tumor was colorectal in 21 %, ovarian in 19 %, pseudomyxoma peritonei in 16 %, an appendix
tumor in 16 %, gastric cancer in 10 %, and peritoneal mesothelioma in 13 % of cases. Mean peritoneal carcinomatosis index
was 22 (range 2–39). Mean global health status score was 69 ± 25 preoperatively and 55 ± 20, 66 ± 22, 66 ± 23, 71 ± 23, and
78 ± 21 at months 1, 6, 12, 24, and 36, respectively. Physical and role function recovered significantly at 6 months and were
close to baseline at the 24-month measurement. Emotional function starting from a low baseline recovered to baseline by month
12. Cognitive and social function had slow recovery on follow-up. Fatigue, diarrhea, dyspnea, and sleep disturbance were symptoms
persistent at 6-month follow-up, improving later on in survivors.

Conclusions  

Survivors after CRS and HIPEC have postoperative quality of life similar to preoperatively, with most of the reduced elements
recovering after 6–12 months. We conclude that reduced quality of life of patients after CRS and HIPEC should not be used
as an argument to deny surgical therapy to these patients.

Ovarian cancer: emerging molecular-targeted therapies June 2012

‘Real inequalities’ a threat to medicare’s mission, incoming CMA chief says - The Globe and Mail

From The Globe and Mail:
'Real inequalities' a threat to medicare's mission, incoming CMA chief 

National Guideline Clearinghouse | Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.

Electronic health records: what does your signature signify?

Ovarian Cancer Clinical Trial: Patient Reported Symptoms in Ovarian Cancer (PRECISION) - ongoing

http://clinicaltrialsfeeds.org/clinical-trials/show/NCT01422265

Public funding for genomics: where does Canada stand?

Public funding for genomics: where does Canada stand?

After more than six years of funding exclusive projects in forestry and agriculture, Genome Canada has now announced a $67.5 million funding competition for large-scale genomics projects in human health, with focus on personalised medicine.ⁱ The human genomics community of this country understandably rejoiced at this long overdue announcement that gives them, for the first time in years, the means to compete internationally (http://www.genomecanada.ca/en/portfolio/research/2012-competition.aspx). Canada has been fairly generous in funding human-health related research but mostly through the Canadian Institutes of Health Research (CIHR) or the Canada Foundation for Innovation, neither of which has within its mandate to fund the type of specific multimillion-dollar project that is usually thought of as genomics. The typical CIHR grant, for example, rarely exceeds $1 million (200 000 over 5 years) in direct costs.

The elation over the announcement of this funding opportunity in late 2011 soon gave way to sober...

Postmenopausal hormone therapy and colorectal cancer risk by molecularly defined subtypes among older women

Postmenopausal hormone therapy and colorectal cancer risk by molecularly defined subtypes among older women

Background

Postmenopausal hormone (PMH) therapy may reduce colorectal cancer (CRC) risk, but existing data are inconclusive.

Objectives

To evaluate associations between PMH therapy and incident CRC, overall and by molecularly defined subtypes, in the population-based Iowa Women's Health Study of older women.

Methods

Exposure data were collected from Iowa Women's Health Study participants (55–69 years) at baseline (1986). Archived, paraffin-embedded tissue specimens for 553 CRC cases were collected and analysed to determine microsatellite instability (MSI-L/MSS or MSI-H), CpG island methylator phenotype (CIMP-negative or CIMP-positive) and BRAF mutation (BRAF-wildtype or BRAF-mutated) status. Multivariable Cox regression models were fit to estimate RRs and 95% CIs.

Results

PMH therapy (ever vs never use) was inversely associated with incident CRC overall (RR=0.82; 95% CI 0.72 to 0.93), with a significantly lower risk for MSI-L/MSS tumours (RR=0.75; 95% CI 0.60 to 0.94), and borderline significantly lower risks for CIMP-negative (RR=0.79; 95% CI 0.63 to 1.01) and BRAF-wildtype (RR=0.83; 95% CI 0.66 to 1.04) tumours. For PMH therapy >5 years, the subtype-specific risk estimates for MSI-L/MSS, CIMP-negative and BRAF-wildtype tumours were: RR=0.60, 95% CI 0.40 to 0.91; RR=0.68, 95% CI 0.45 to 1.03; and RR=0.70, 95% CI 0.47 to 1.05, respectively. PMH therapy was not significantly associated with the MSI-H, CIMP-positive or BRAF-mutated CRC subtypes.

Conclusions

In this prospective cohort study, PMH therapy was inversely associated with distinct molecularly defined CRC subtypes, which may be related to differential effects from oestrogen and/or progestin on heterogeneous pathways of colorectal carcinogenesis.

Sequential whole-body PET/MR scanner: concept, clinical use, and optimisation after two years in the clinic. The manufacturer’s perspective

Sequential whole-body PET/MR scanner: concept, clinical use, and optimisation after two years in the clinic. The manufacturer's perspective

Abstract  

PET and MRI are established clinical tools which provide complementary information, but clinical workflow limits widespread
clinical application of both modalities in combination. The two modalities are usually situated in different hospital departments
and operated and reported independently, and patients are referred for both scans, often consecutively. With the advent of
PET/MR as a new hybrid imaging modality there is now a possibility of addressing these concerns. There are two different design
philosophies for integrated PET/MR imaging—positioning PET inside the MRI magnet or in tandem, similar to PET/CT. The Ingenuity
TF PET/MR by Philips Healthcare is a sequential PET/MR tomograph combining state-of-the-art time-of-flight PET and high-field
MRI with parallel transmission capabilities. In this review article we describe the technology implemented in the system,
for example RF and magnetic shielding, MR-based attenuation correction, peculiarities in scatter correction, MR system optimisation,
and the philosophy behind its design. Furthermore, we provide an overview of how the system has been used during the last
two years, and expectations of how the use of PET/MR may continue in the years to come. On the basis of these observations
and experiences we discuss the utility of the system, clinical workflow and acquisition times, and possible ways of optimization.

• Content Type Journal Article
• Category Review Article
• Pages 1-19
• DOI 10.1007/s10334-012-0330-y

• Journal Magnetic Resonance Materials in Physics, Biology and Medicine

Oncology imaging in the abdomen and pelvis: where cancer hides

Oncology imaging in the abdomen and pelvis: where cancer hides

Abstract  

As the incidence of cancer continues to increase, imaging will play an ever more important role in the detection, diagnosis,
staging, surveillance, and therapeutic monitoring of cancer. Diagnostic errors in the initial discovery of cancer or at follow-up
assessments can lead to missed opportunities for curative treatments or altering or reinitiating therapies, as well as adversely
impact clinical trials. Radiologists must have an understanding of cancer biology, treatments, and imaging appearance of therapeutic
effects and be mindful that metastatic disease can involve virtually any organ system. Knowledge of patient history and tumor
biology allows for optimizing imaging protocols. The majority of cancer imaging utilizes computed tomography, where contrast
enhancement characteristics of lesions can be exploited and detection of subtle lesions can involve manipulation of window
width and level settings, multiplanar reconstruction, and maximum intensity projections. For magnetic resonance imaging, diffusion-weighted
imaging can render lesions more conspicuous, improve characterization, and help assess therapeutic response. Positron emission
tomography with ¹⁸F-labeled fluorodeoxyglucose and sodium fluoride are invaluable in detecting occult existing and new cancerous lesions, characterizing
indeterminate lesions, and assessing treatment effects. The most common anatomic "hiding places" for cancer include metastases
to solid organs, such as the kidneys and pancreas, gastrointestinal tract, peritoneum and retroperitoneum, neural axis, muscular
body wall, and bones. Consistent work habits, employment of appropriate technologies, and particular attention to the above
anatomic areas can enhance detection, staging, and reassessments of these complex and often stealthy diseases, ensuring the
radiologists' integral role in the cancer care team.

• Journal Abdominal Imaging
• Online ISSN 1432-0509

Journal of Cancer Education - SpringerLink

http://www.springerlink.com/content/121578/


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Dietary Lifestyle and Colorectal Cancer Onset, Recurrence, and Survival: Myth or Reality?

Dietary Lifestyle and Colorectal Cancer Onset, Recurrence, and Survival: Myth or Reality?

Abstract

Background and Purpose  

Interest in the possibility that diet might help to reduce the risk of colorectal cancer dates back to 1970 based on both
the large variation in rates of specific cancers in different countries and the impressive changes observed in the incidence
of cancer in migrants from low- to high-risk areas. Here, we report the state of art of literature data about this topic.

Methods  

Three sections have been separately considered: chemoprevention of first tumor onset, chemoprevention of recurrence after
surgery, and chemoprevention of polyp recurrence in the course of the follow-up of subjects with elevated risk. A particular
attention has been pointed to dietary factors and survival, whose relevance is showing a growing interest.

Results  

The relationship between diet and colorectal cancer has been extensively studied about the onset, sometimes with controversial
results. Its influence on recurrence and survival has been examined in only few studies.

Conclusions  

Literature data are convincing for a protective role on the onset of preneoplastic and neoplastic lesions for some foods such
as fibers, vitamin A and D, folic acid, calcium, antioxidants, and promising perspectives for some substances such as phyto-estrogens.
Less evidence-based data are available on the possibility to avoid the recurrence of the disease or to affect its mortality
with dietary habits. Future perspectives will be directed be not only to identify new dietary style able to prevent the onset
of neoplastic lesion of the colon but also to realize an effective chemoprevention.

• Content Type Journal Article
• Category Review Article
• Pages 1-11
• DOI 10.1007/s12029-012-9425-y

A prospective study of the feasibility and acceptability of a Web-based, electronic patient-reported outcomes system in assessing patient recovery after major gynecologic cancer surgery.

http://www.ncbi.nlm.nih.gov/m/pubmed/22871467/

Ovarian Cancer Biotargets of Cancer in Current Clinical Practice

Ovarian Cancer Biotargets of Cancer in Current Clinical Practice

In Biotargets of Cancer in Current Clinical Practice (2012), pp. 381-401, doi:10.1007/978-1-61779-615-9_14

Ovarian cancer is the fifth most common cancer in women and is the most lethal of all gynecologic cancers. Early-stage ovarian cancer is curable while women who are diagnosed with advanced ovarian cancer continue to have poor long-term survival due to recurrence of disease. Unfortunately, most women are diagnosed with advanced-stage disease. Early detection is a primary objective for clinicians and scientists, yet single modality (CA-125, transvaginal ultrasound) screening tests have been ineffective. More recent novel approaches combining modalities and utilizing serial serum sampling are being tested and hold great promise. In addition, the recent application of proteomics to this clinical question has the potential to identify new and important biotargets. Unfortunately, the majority of ovarian cancer patients have advanced-stage disease, and although most will die of their disease, their survival is quite heterogenous. The ability to stratify patients according to prognosis could help guide therapy. The current "gold standard" for prognosis uses patient, surgical, and tumor characteristics, yet these have the tendency to be notoriously inaccurate. This prognostic uncertainty and the drive to identify predictive factors by which we can select novel and targeted therapy have stimulated researchers to look beyond traditional markers and test and validate molecular and genomic biomarkers, which are anticipated to soon complement or even eclipse traditional factors clarifying prognosis and select treatments. For patients with advanced-stage disease, a multitude of prognostic factors have been characterized. While promising, none of these biotargets have been validated at present to be clinically useful. More recent application of genomic technologies is likely to yield clinically relevant signatures and/or biotargets which will provide the basis for personalization of care for these patients.
Jessica Oribabor, Allison Ambrosio, Cesar Castro, Michael Birrer

Environmentally Induced Epigenetic Transgenerational Inheritance of Ovarian Disease

"Environmentally Induced Epigenetic Transgenerational Inheritance of Ovarian Disease"

Incidence, appropriateness, and consequences of recommendations for additional imaging tests in oncological PET/CT reports

Incidence, appropriateness, and consequences of recommendations for additional imaging tests in oncological PET/CT reports

Publication year: 2012
Source:Clinical Radiology
A.B. Shinagare, P.B. Shyn, C.A. Sadow, E.J. Wasser, P. Catalano
Aim To assess the incidence, appropriateness, and outcomes of recommendations for additional imaging tests (RAI) in oncological combined 2-[¹⁸F]-fluoro-2-deoxy-d-glucose positron-emission tomography and computed tomography (FDG-PET/CT) reports. Material and methods In this retrospective study, conducted with institutional review board approval, the first oncological FDG-PET/CT reports in 2008 for 250 consecutive patients were reviewed to identify RAI. PET/CT reports containing RAI were retrospectively reviewed by two blinded readers. PET/CT findings prompting RAI, appropriateness of RAI, results of additional imaging tests actually performed, and the ultimate clinical significance of findings prompting RAI were recorded. Confirmation of clinical significance required pathology confirmation, unequivocal imaging progression, imaging stability for 12 months, or clinical follow-up for 24 months or end of life. Results Eighty-four RAI were identified for 88 PET/CT findings in 29.6% (74/250) of PET/CT reports, of which 51.2% (43/84) were deemed unnecessary by reviewers. Referring clinicians only followed 31% (26/84) of RAI by requesting additional imaging tests, and these tests resolved the PET/CT question in 76.9% (20/26) of those cases. Only 11.4% (10/88) of all findings prompting RAI proved to be clinically significant. Only 4.7% (2/43) of RAI deemed unnecessary by reviewers and 5.2% (3/58) of RAI not pursued by clinicians were found to be clinically significant; however, PET/CT alone was sufficient for diagnosis or guiding appropriate clinical management in each of these cases. Conclusion RAI were found in 29.6% of oncological PET/CT reports. No potential adverse impact on patient management or outcome, by not issuing or following RAI, was identified in the 51.2% of RAI deemed unnecessary by study readers or in the 69% of RAI not pursued by referring clinicians.

Hormone replacement therapy after breast cancer: 10 year follow up of the Stockholm randomised triall

Hormone replacement therapy after breast cancer: 10 year follow up of the Stockholm randomised trial

Publication year: 2012
Source:European Journal of Cancer
Mia Fahlén, Tommy Fornander, Hemming Johansson, Ulla Johansson, Lars-Erik Rutqvist, Nils Wilking, Eva von Schoultz
Background The management of hormonal deficiency symptoms in breast cancer survivors is an unsolved problem. While hormone replacement therapy (HRT) may increase the risk of breast cancer in healthy women, its effects on recurrence is unclear. Observational studies have suggested decreased recurrence rates from HRT. The few clinical trials in this field have all been closed preterm. Methods The Stockholm trial was started in 1997 and designed to minimise the dose of progestogen in the HRT arm. Disease-free women with a history of breast cancer were randomised to HRT (n =188) or no HRT (n =190). The trial was stopped in 2003 when another Swedish study (HABITS, the Hormonal Replacement After Breast Cancer – Is it Safe?) reported increased recurrence. However the Stockholm material showed no excess risk after 4years of follow-up. A long term follow-up has now been performed. Findings After 10.8years of follow-up, there was no difference in new breast cancer events: 60 in the HRT group versus 48 among controls (hazard ratio (HR)=1.3; 95% confidence interval (CI)=0.9–1.9). Among women on HRT, 11 had local recurrence and 12 distant metastases versus 15 and 12 for the controls. There were 14 contra-lateral breast cancers in the HRT group and four in the control group (HR=3.6; 95% CI=1.2–10.9; p =0.013). No differences in mortality or new primary malignancies were found. Interpretation The number of new events did not differ significantly between groups, in contrast to previous reports. The increased recurrence in HABITS has been attributed to higher progestogen exposure. As both trials were prematurely closed, data do not allow firm conclusions. Both studies found no increased mortality from breast cancer or other causes from HRT. Current guidelines typically consider HRT contraindicated in breast cancer survivors. Findings suggest that, in some women symptom relief may outweigh the potential risks of HRT.

Whole mind and shared mind in clinical decision-making

Whole mind and shared mind in clinical decision-making

Publication year: 2012
Source:Patient Education and Counseling
Ronald Mark Epstein
Objective To review the theory, research evidence and ethical implications regarding "whole mind" and "shared mind" in clinical practice in the context of chronic and serious illnesses. Methods Selective critical review of the intersection of classical and naturalistic decision-making theories, cognitive neuroscience, communication research and ethics as they apply to decision-making and autonomy. Results Decision-making involves analytic thinking as well as affect and intuition ("whole mind") and sharing cognitive and affective schemas of two or more individuals ("shared mind"). Social relationships can help processing of complex information that otherwise would overwhelm individuals' cognitive capacities. Conclusions Medical decision-making research, teaching and practice should consider both analytic and non-analytic cognitive processes. Further, research should consider that decisions emerge not only from the individual perspectives of patients, their families and clinicians, but also the perspectives that emerge from the interactions among them. Social interactions have the potential to enhance individual autonomy, as well as to promote relational autonomy based on shared frames of reference. Practice implications Shared mind has the potential to result in wiser decisions, greater autonomy and self-determination; yet, clinicians and patients should be vigilant for the potential of hierarchical relationships to foster coercion or silencing of the patient's voice.

Addressing the Financial Consequences of Cancer: Qualitative Evaluation of a Welfare Rights Advice Service

Addressing the Financial Consequences of Cancer: Qualitative Evaluation of a Welfare Rights Advice Service

by Suzanne Moffatt, Emma Noble, Martin White

Background

The onset, treatment and trajectory of cancer is associated with financial stress among patients across a range of health and welfare systems and has been identified as a significant unmet need. Welfare rights advice can be delivered effectively in healthcare settings, has the potential to alleviate financial stress, but has not yet been evaluated. We present an evaluation of a welfare rights advice intervention designed to address the financial consequences of cancer.

Methods

Descriptive study of welfare outcomes among 533 male and 641 female cancer patients and carers aged 4–95 (mean 62) years, who accessed the welfare rights advice service in North East England between April 2009 and March 2010; and qualitative interview study of a maximum variation sample of 35 patients and 9 carers.

Results

Over two thirds of cancer patients and carers came from areas of high socio-economic deprivation. Welfare benefit claims were successful for 96% of claims made and resulted in a median increase in weekly income of £70.30 ($109.74, €84.44). Thirty-four different types of benefits or grants were awarded. Additional resources were perceived to lessen the impact of lost earnings, help offset costs associated with cancer, reduce stress and anxiety and increase ability to maintain independence and capacity to engage in daily activities, all of which were perceived to impact positively on well-being and quality of life. Key barriers to accessing benefit entitlements were knowledge, system complexity, eligibility concerns and assumptions that health professionals would alert patients to entitlements.

Conclusions

The intervention proved feasible, effectively increased income for cancer patients and was highly valued. Addressing the financial sequelae of cancer can have positive social and psychological consequences that could significantly enhance effective clinical management and suitable services should be routinely available. Further research is needed to evaluate health outcomes definitely and assess cost-effectiveness.

"The Coach And The Critic" Blog Comes To Life Online: A Discussion About Caregivers That I Will Never Forget

http://m.cancer.org/AboutUs/DrLensBlog/post/2011/04/26/The-Coach-And-The-Critic-Blog-Comes-To-Life-Online-A-Discussion-About-Caregivers-That-I-Will-Never-Forget.aspx

Safety, cost-effectiveness and feasibility of daycase paracentesis in the management of malignant ascites with a focus on ovarian cancer.

Safety, cost-effectiveness and feasibility of daycase paracentesis in the management of malignant ascites with a focus on ovarian cancer.

Safety, cost-effectiveness and feasibility of daycase paracentesis in the management of malignant ascites with a focus on ovarian cancer.

Br J Cancer. 2012 Aug 9;

Authors: Harding V, Fenu E, Medani H, Shaboodien R, Ngan S, Li HK, Burt R, Diamantis N, Tuthill M, Blagden S, Gabra H, Urch CE, Moser S, Agarwal R

Abstract

Background:Paracentesis for malignant ascites is usually performed as an in-patient procedure, with a median length of stay (LoS) of 3-5 days, with intermittent clamping of the drain due to a perceived risk of hypotension. In this study, we assessed the safety of free drainage and the feasibility and cost-effectiveness of daycase paracentesis.Method:Ovarian cancer admissions at Hammersmith Hospital between July and October 2009 were audited (Stage 1). A total of 21 patients (Stage 2) subsequently underwent paracentesis with free drainage of ascites without intermittent clamping (October 2010-January 2011). Finally, 13 patients (19 paracenteses, Stage 3), were drained as a daycase (May-December 2011).Results:Of 67 patients (Stage 1), 22% of admissions and 18% of bed-days were for paracentesis, with a median LoS of 4 days. In all, 81% of patients (Stage 2) drained completely without hypotension. Of four patients with hypotension, none was tachycardic or symptomatic. Daycase paracentesis achieved complete ascites drainage without complications, or the need for in-patient admission in 94.7% of cases (Stage 3), and cost £954 compared with £1473 for in-patient drainage.Conclusions:Free drainage of malignant ascites is safe. Daycase paracentesis is feasible, cost-effective and reduces hospital admissions, and potentially represents the standard of care for patients with malignant ascites.British Journal of Cancer advance online publication, 9 August 2012; doi:10.1038/bjc.2012.343 www.bjcancer.com.

PMID: 22878372 [PubMed - as supplied by publisher]

Factors Associated with Publication of Plenary Presentations at the Society of Gynecologic Oncologists Annual Meeting

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Factors Associated with Publication of Plenary Presentations at the Society of Gynecologic Oncologists Annual Meeting

Publication year: 2012

Objective To determine the rate and factors associated with publication of plenary abstract presentations from the Society of Gynecologic Oncologists annual meeting. Methods Plenary presentations were reviewed from 2000 to 2005. A Pubmed search was performed to identify subsequent peer-reviewed publication of these presentations. Chi-squared test and logistic regression were used for statistical analyses. Results Of 378 main, focused or express plenary presentations, 173 (45.8%) involved multiple and 205 (54.2%) single institutions. The types of study include: chart review (29.4%), cohort study (28.0%), translational (23.5%), and randomized clinical trial (6.9%). 309 (81.7%) of presentations were subsequently published. The median time from presentation to publication was 14months (range: 1–85). Studies from multiple vs. single institutions were more likely to be published (87.9% vs. 76.6%; p=0.005). In addition, randomized controlled trials were more likely to be published compared to chart review, cohort, and translation research (92.3% vs. 83.8%, 77.4%, and 74.2%; p<0.01). On multivariate analysis, multi-institutional studies (OR=2.28, 95% CI=1.28-4.04; p=0.005) and type of study (OR=1.64, 95% CI=1.19-2.26; p=0.002) were independent factors associated with publication. In addition, multi-institutional studies had longer times from presentation to publication compared to their counterparts. Conclusions A high percentage of plenary presentations at the Society of Gynecologic Oncologists annual meeting resulted in subsequent publication. Multi-institutional studies and randomized clinical trials were more likely to be published.

Highlights

► Over 80% of presentations at the annual Society of Gynecologic Oncologists meeting were published in peer-reviewed journals ► Single-institution studies were associated with a lower likelihood of publication ► Multi-institutional studies had a higher publication rate compared to other studies

Psychological treatment outcomes for cancer patients: what do meta-analyses tell us about distress reduction?

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Psychological treatment outcomes for cancer patients: what do meta-analyses tell us about distress reduction?

Psychological treatment outcomes for cancer patients: what do meta-analyses tell us about distress reduction?

Psychooncology. 2012 Apr;21(4):343-50

Abstract

OBJECTIVE: The effectiveness of psychological treatment for distress reduction in cancer patients has been frequently studied and reviewed in systematic reviews but reviewer conclusions vary considerably. Clear and consistent evidence is needed to assist clinicians and administrators with their decision-making. We hypothesized that uneven handling of confounding methodological features are at least partly the reason for disagreements and reviewed the literature in this light.

METHOD: A systematic review of 14 published meta-analyses was conducted to determine whether due consideration of moderating variables in psycho-oncological treatments permits clearer recommendations. Quality of the reviews, treatment type, dosage, therapist qualities, outcomes at follow-up, and screening versus not screening for elevated distress were examined as moderator variables.

RESULTS: Treatment effects are consistently positive but also vary greatly in magnitude. There is lacking evidence for many important questions, in particular, differential treatment effects for different cancer types and stages. Regarding moderators of outcome, quality of review had no impact on results for depression but including lower quality reviews actually lead to underestimation of treatment effects for anxiety. The most potent negative moderator variable, however, is a floor effect that arises when patients are recruited for treatment studies without being selected for high levels of distress. Such indiscriminate recruitment is very frequent in psycho-oncology and leads to small reported treatment effects; when, however, patients are first screened for elevated distress, the ratio of observed treatment effects sizes is roughly three times greater.

CONCLUSION: Sweeping judgments about the effectiveness of psycho-oncological treatments for distress reduction are somewhat misleading and counter-productive. Among moderator variables, floor effects are particularly pervasive and have a large suppressor effect on observed outcomes.

PMID: 21882287 [PubMed - indexed for MEDLINE]

Management of highly emetogenic chemotherapy

Recurrent ovarian cancer: Is there a role for re-treatment with bevacizumab after an initial complete response to a bevacizumab-containing regimen?

Recurrent ovarian cancer: Is there a role for re-treatment with bevacizumab after an initial complete response to a bevacizumab-containing regimen?

Publication year: 2012
Source:Gynecologic Oncology
Georgia A. McCann, Blair Smith, Floor J. Backes, Kellie Rath, Simi Chacko, Ritu Salani, Eric Eisenhauer, Jeffrey Fowler, David Cohn, David O'Malley
Objective To compare the progression free survival (PFS) and overall survival (OS) in patients with epithelial ovarian cancer (EOC) who received Bev after Bev (BAB) versus those who were not re-treated with Bev (NOTBev) after initially experiencing a complete response (CR) to a Bev-containing regimen (BCR). Methods We performed a retrospective chart review of patients with EOC that received Bev in either the front-line or recurrent setting. Patients who received additional therapy after achieving a CR to BCR were analyzed. Results 36 patients who had a CR to a BCR were included, 17 who received Bev at the time of their subsequent recurrence versus 19 that did not. More patients in the NOTBev group received Bev as primary therapy (21% vs. 6%, p=0.2), but this was not statistically significant. Patients in the BAB group had significantly higher mean PFS compared to the NOTBev group (20 vs. 6months, p=0.0019). On adjusting for covariates, there was a 78% improvement in their PFS (HR 0.22, p=0.0048). No difference in overall survival was noted between the groups (23 vs. 26months, p=0.7244). Conclusions Re-treatment with Bev after a prior Bev response is associated with a significantly improved PFS. This is the first of such reports in this patient population. The 14-month improvement in PFS strongly supports the re-use of Bev in patients who demonstrate an initial response to Bev. This strategy should be formally tested in future clinical trials and further investigation should include evaluation of predictors of response to Bev therapy.

Highlights

► Comparison of patients who were treated with Bev versus not after CR on Bev. ► The use of Bev after CR on Bev increased the PFS versus no subsequent Bev. ► The use of Bev after CR on Bev did not impact OS versus no subsequent Bev.

The biology of ovarian cancer: new opportunities for translation

The biology of ovarian cancer: new opportunities for translation

Nature Reviews Cancer, Vol. 9, No. 6. (01 June 2009), pp. 415-428, doi:10.1038/nrc2644

Over the past two decades, the 5-year survival for ovarian cancer patients has substantially improved owing to more effective surgery and treatment with empirically optimized combinations of cytotoxic drugs, but the overall cure rate remains approximately 30%. Many investigators think that further empirical trials using combinations of conventional agents are likely to produce only modest incremental improvements in outcome. Given the heterogeneity of this disease, increases in long-term survival might be achieved by translating recent insights at the molecular and cellular levels to personalize individual strategies for treatment and to optimize early detection.
Robert Bast, Bryan Hennessy, Gordon Mills

Humanities aren’t a science. Stop treating them like one. | Literally Psyched, Scientific American Blog Network

.....The tools of mathematical and statistical and scientific analysis are invaluable. But their quantifiable certainty is all too easy to see as the only "real" way of doing things when really, it is but one tool and one approach—and not one that is translatable or applicable to all matters of qualitative phenomena. That's one basic fact we'd do well not to forget."


http://blogs.scientificamerican.com/literally-psyched/2012/08/10/humanities-arent-a-science-stop-treating-them-like-one/


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Individualized care best for lymphedema patients, MU researcher says

http://www.eurekalert.org/pub_releases/2012-08/uom-icb081012.php

Management of a suspicious adnexal mass - PubMed Mobile

http://www.ncbi.nlm.nih.gov/m/pubmed/22876153/

Management of a suspicious adnexal mass: a clinical practice guideline.

Authors

Dodge JE, et al. Show all

Journal

Curr Oncol. 2012 Aug;19(4):e244-e257.

Affiliation

Division of Gynaecologic Oncology, Princess Margaret Hospital, University Health Network, Department of Obstetrics and Gynaecology, Toronto, ON.

Abstract

QUESTIONS: What is the optimal strategy for preoperative identification of the adnexal mass suspicious for ovarian cancer? What is the most appropriate surgical procedure for a woman who presents with an adnexal mass suspicious for malignancy?....

July 18th, 2012: Uncertain Genetic Test Results for Lynch Syndrome - Full Text View - ClinicalTrials.gov

Uncertain Genetic Test Results for Lynch Syndrome - Full Text View - ClinicalTrials.gov

This study is currently recruiting participants.

Verified April 2012 by National Institutes of Health Clinical Center (CC)

First Received on July 18, 2012.   No Changes Posted

Sponsor:	National Human Genome Research Institute (NHGRI)
Information provided by:	National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:	NCT01646112

  Purpose

Background:

• Individuals have varying tolerances for receiving ambiguous information. However, not much is known about how ambiguous genetic testing information is received. Also, not much is known about how at-risk individuals internalize and process these results. More information is needed about how this information affects a person's life.
• Lynch Syndrome is a genetic condition that carries a high risk of colon cancer and other cancers. Individuals at risk for Lynch Syndrome can have genetic testing for it. The test may confirm a diagnosis and determine actions that can be taken. Results from genetic testing can also affect the perspectives of relatives who might also be affected. However, genetic testing can also produce variants of unknown significance (VUS). VUS are data that may not provide enough information to make decisions. Researchers want to study people who have received a VUS result for genetic testing for Lynch Syndrome.

Objectives:

- To learn more about the impact and experience of receiving a VUS for Lynch Syndrome genetic testing.

Eligibility:

- Individuals at least 18 years of age who have recently had a VUS result on a genetic test for Lynch Syndrome.

Design:

• Participants will be asked to answer demographic questions. They will also have a 45- to 60-minute phone interview.
• During the phone interview, participants will be asked a series of questions about their diagnosis. They will be asked about how they received the result and how they felt right after receiving it. They will also discuss who they have spoken to about the result.

ongoing: Anonymous Testing of Pathology Specimens for BRCA Mutations in Ashkenazi Jewish Individuals Who Have Cancer - Full Text View - ClinicalTrials.gov

Anonymous Testing of Pathology Specimens for BRCA Mutations in Ashkenazi Jewish Individuals Who Have Cancer - Full Text View - ClinicalTrials.gov

Anonymous Testing of Pathology Specimens for BRCA Mutations in Ashkenazi Jewish Individuals Who Have Cancer

This study is currently recruiting participants.

Verified July 2012 by Memorial Sloan-Kettering Cancer Center

First Received on December 22, 2007.   Last Updated on July 23, 2012   History of Changes

Sponsor:	Memorial Sloan-Kettering Cancer Center
Information provided by (Responsible Party):	Memorial Sloan-Kettering Cancer Center
ClinicalTrials.gov Identifier:	NCT00588263

  Purpose

The intent of the proposed study is to describe the prevalence of the most common recurring mutations in BRCA1 and BRCA2, blmAsh , and the A636P MSH2 mutation among Ashkenazi Jewish individuals with a variety of cancer diagnoses. If a substantial proportion of these samples contain such mutations, future patients presenting with these diseases may wish to undergo genetic counseling and, if appropriate, formal genetic testing. The benefit from such a process would pertain mainly to the families of these individuals.

Condition
Extrahepatic Bile Duct Cancer Gallbladder Cancer Gastric Cancer Lung Cancer Melanoma Non-Hodgkin's Lymphoma Uterine Cancer CORPUS UTERI,ENDOMETRIUM LUNG OVARY

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Prospective
Official Title:	Anonymous Testing of Pathology Specimens for BRCA Mutations in Ashkenazi Jewish Individual With Cancer

Are Opinions Based on Science: Modelling Social Response to Scientific Facts

Are Opinions Based on Science: Modelling Social Response to Scientific Facts:

by Gerardo Iñiguez, Julia Tagüeña-Martínez, Kimmo K. Kaski, Rafael A. Barrio

As scientists we like to think that modern societies and their members base their views, opinions and behaviour on scientific facts. This is not necessarily the case, even though we are all (over-) exposed to information flow through various channels of media, i.e. newspapers, television, radio, internet, and web. It is thought that this is mainly due to the conflicting information on the mass media and to the individual attitude (formed by cultural, educational and environmental factors), that is, one external factor and another personal factor. In this paper we will investigate the dynamical development of opinion in a small population of agents by means of a computational model of opinion formation in a co-evolving network of socially linked agents. The personal and external factors are taken into account by assigning an individual attitude parameter to each agent, and by subjecting all to an external but homogeneous field to simulate the effect of the media. We then adjust the field strength in the model by using actual data on scientific perception surveys carried out in two different populations, which allow us to compare two different societies. We interpret the model findings with the aid of simple mean field calculations. Our results suggest that scientifically sound concepts are more difficult to acquire than concepts not validated by science, since opposing individuals organize themselves in close communities that prevent opinion consensus.................

Putting respect to work : The Lancet

Putting respect to work : The Lancet

The Lancet, Volume 380, Issue 9841, Page 564, 11 August 2012

<Previous Article|Next Article>

doi:10.1016/S0140-6736(12)61330-0Cite or Link Using DOI

Putting respect to work

Edmund Dunstan a

There is an aspect of dignity that Charles Foster (June 2, p 2044)1 does not address. I found the term vague and unhelpful until I heard Gordon Lishman, former Director-General of Age Concern England, remark how whereas professionals often used the term “dignity”, the word older people themselves used was usually “respect”. In Latin the word dignus means “worthy”. Surely, our obligation is to show people the respect, whether in word or deed, that gives them dignity—the subjective experience of their own worth.

We can explore the implications for this in the scenarios Foster describes. In the case of the patient in the vegetative state undergoing vaginal examinations we could reasonably assume that her sense of worth would be impaired if she were aware of what was going on; for the brain-damaged teenager we have the difficult choice of whether to presume that her standards are ours—or accept her apparent behaviour that she does not mind; but the owner of the skull used as a drinking vessel can have no sense of worth—although we might regard the behaviour as in poor taste.

 

I declare that I have no onflicts of interest.

Reference

1 Foster C. Putting dignity to work. Lancet 2012; 379: 2044-2045. Full Text | PDF(150KB) | CrossRef | PubMed

European Journal of Human Genetics - Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

http://www.nature.com/ejhg/journal/v19/n1s/full/ejhg2010249a.html

Cancer care services don't differ by neighborhood

http://reut.rs/S3ffBr

HIN-1 clear cell ovarian cancer

CONCLUSIONS: Methylation of HIN-1 and CACNA1A promoters are two novel epigenetic biomarkers associated with poor outcomes in OCCA patients. Ectopic expression of the HIN-1 gene increased paclitaxel sensitivity through Akt pathway

http://www.google.ca/reader/i/?source=mog&hl=en&gl=ca#stream/search%2FOvarian


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A Retrospective Study Evaluating Frequency and Risk Factors of Osteonecrosis of the Jaw in 576 Cancer Patients Receiving Intravenous Bisphosphonates

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A Retrospective Study Evaluating Frequency and Risk Factors of Osteonecrosis of the Jaw in 576 Cancer Patients Receiving Intravenous Bisphosphonates

Retrospective analysis of 576 cancer patients treated with intravenous bisphosphonates found that 3.1% developed osteonecrosis of the jaw, 59% of which followed tooth extraction. Diabetes, hypothyroidism,...

Patterns of Gene Expression That Characterize Long-term Survival in Advanced Stage Serous Ovarian Cancers

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Patterns of Gene Expression That Characterize Long-term Survival in Advanced Stage Serous Ovarian Cancers

Clinical Cancer Research In Clinical Cancer Research, Vol. 11, No. 10. (15 May 2005), pp. 3686-3696, doi:10.1158/1078-0432.CCR-04-2398

Purpose: A better understanding of the underlying biology of invasive serous ovarian cancer is critical for the development of early detection strategies and new therapeutics. The objective of this study was to define gene expression patterns associated with favorable survival.
Andrew Berchuck, Edwin Iversen, Johnathan Lancaster, Jennifer Pittman, Jingqin Luo, Paula Lee, Susan Murphy, Holly Dressman, Phillip Febbo, Mike West, Joseph Nevins, Jeffrey Marks

Komen founder to leave CEO role but stay on in management

http://reut.rs/OUnMWY

State of the Science in Ovarian Cancer Quality of Life Research: A Systematic Review

State of the Science in Ovarian Cancer Quality of Life Research: A Systematic Review

Hess, Lisa M. PhD; Stehman, Frederick B. MD

International Journal of Gynecological Cancer . POST AUTHOR CORRECTIONS, 6 August 2012

doi: 10.1097/IGC.0b013e318263f02e

Abstract

Introduction: Health-related quality of life (HRQOL) has become an increasingly important focus of outcomes in cancer care with the movement toward more patient-oriented research. Quality-of-life outcomes are important in ovarian cancer, which has not yet benefitted from improved survival outcomes as have other diseases. This study was designed to systematically assess and summarize HRQOL in ovarian cancer.

Methods: A systematic search strategy was initiated to identify published literature measuring HRQOL of women with a diagnosis of ovarian cancer (OC). Data were synthesized to evaluate HRQOL and patient-reported outcome data at various time points: before, during, and after chemotherapy. Data were pooled and summary statistics compared across published studies. Comparisons of means were conducted using analysis of variance.

Results: There were 170 publications meeting all eligibility criteria, representing 139 unique studies of patients with ovarian cancer, where QOL data were collected. Within this literature, more than 90 different patient-reported outcome (PRO) instruments were administered. The most common HRQOL instruments included the European Organisation for Research and Treatment of Cancer QLQ-C30 and the Functional Assessment of Cancer Therapy. Few studies alone demonstrated significant differences in QOL between the experimental and comparison arm or throughout the treatment period. Pooled data, however, show that baseline QOL may significantly improve, particularly after completion of chemotherapy treatment.

Discussion: Despite the increase in assessment and reporting of QOL in ovarian cancer research studies during the past 15 years, there remains little consistency in the types and format of data collected. There is a need to enhance the standardized collection and reporting of HRQOL data from research involving women with ovarian cancer so that research can build on the cumulative knowledge base to improve outcomes in this patient population.

http://mobile.journals.lww.com/ijgc/_layouts/oaks.journals.mobile/abstractviewer.aspx?year=9000&issue=00000&article=99473

No Proven Benefit For PET And PET/CT In Ovarian Cancer

Ann_Oncology: Maternal and fetal outcomes of taxane chemotherapy in breast and ovarian cancer during pregnancy: case series and review of the literature

http://m.annonc.oxfordjournals.org/content/early/2012/08/07/annonc.mds170.short?rss=1?rss=1?rss=1

Health IT for You - Giving You Access to Your Medical Records (3:00 min) | Patients & Families | HealthIT.gov

Health IT for You - Giving You Access to Your Medical Records (3:00 min)

August 7, 2012 | 3:00

Health Information Technology, or Health IT for short, is upgrading our healthcare system for the 21st Century. Today's technology is converting the information in our paper records into an electronic format which allows you and your doctors to have access to your health information when and where it's needed. Learn more about the benefits of health IT and how online, secure access to your health record can help make sure you get the best care.

View the 60-second version of this video.

http://www.healthit.gov/patients-families/video/health-it-you-giving-you-access-your-medical-records

http://www.news-medical.net/news/20120809/Recurrences-of-ovarian-cancer-can-be-detected-earlier-and-more-accurately-with-PETCT.aspx

Recurrences of ovarian cancer can be detected earlier and more accurately with PET/CT

Due to the lack of studies, there is currently no proof that patients with ovarian cancer can benefit from positron emission tomography (PET) alone or in combination with computed tomography (CT). As regards diagnostic accuracy, in certain cases, recurrences can be detected earlier and more accurately with PET or PET/CT than with conventional imaging techniques. This is the conclusion of the final report by the German Institute for Quality and Efficiency in Health Care (IQWiG) in Cologne that was published on 23 May 2012.

More reliable diagnosis is supposed to improve treatment

Ovarian cancer is the fifth most common malignant tumour in women. Every year 15.9 women in every 100,000 are diagnosed with the disease in Germany and it claims the lives of 8 in 100,000 women per year. Since the ovaries lie deep in the abdomen and an ovarian tumour normally causes no symptoms for a long time, it is often only discovered at a late stage.

Many experts hope that an investigation using PET or PET/CT alone or in combination with other methods would be better able to distinguish between benign and malignant tumours when ovarian cancer is suspected. It could also help classify cancerous tumours into the correct stage, make it easier to assess whether they respond to treatment and to show earlier and with greater certainty whether a recurrence or secondary tumour (metastasis) has occurred. This information should then enable patients to be given better treatment recommendations.

Benefit for patients is crucial

IQWiG therefore searched the international literature for studies investigating the effects of diagnosis using PET or PET/CT on health aspects of direct relevance to patients. For example, the results of this research - and an appropriately tailored treatment - could contribute to patients having better chances of survival, spare them unnecessary operations or other diagnostic procedures, or improve their quality of life. However, the search for such studies was unsuccessful, so the question as to the patient-relevant benefit of PET or PET/CT had to remain unanswered.

PET can better detect recurrences in certain cases

In addition, IQWiG searched for studies in which the diagnostic accuracy and prognostic power of PET or PET/CT were compared with other diagnostic methods. The basic question is how often a PET investigation gives a correct result. On the one hand, it should overlook true, cancerous tumours as rarely as possible, but on the other, it should not awake any false suspicions.

A review of hospital characteristics associated

http://www.ncbi.nlm.nih.gov/m/pubmed/22871420/


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