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Wednesday, April 20, 2016

Ultrasound in preoperative assessment of pelvis and abdominal spread in patients with ovarian cancer: a prospective study



abstract
Ultrasound in preoperative assessment of pelvis and abdominal spread in patients with ovarian cancer: a prospective study
 

Objective

To analyze the accuracy of ultrasound in assessing pelvic and intra-abdominal disease in patients with ovarian cancer.

Methods

This prospective study enrolled all consecutive patients referred to a single gynecologic oncology center for suspected ovarian cancer. Only data with histologically confirmed primary ovarian cancer in patients who were evaluated under predefined preoperative ultrasound, intraoperative and pathologic protocols were analyzed. The rectosigmoid wall infiltration depth, peritoneal involvement in different compartments and metastatic lymph node presence were correlated with histopathology.

Results

A total of 578 patients were enrolled from 2008 to 2013; 394 patients met the study criteria and their data were analysed, 74 % of them suffered from advanced stage cancer. Our results showed excellent agreement between ultrasound and histology in rectosigmoid wall infiltration assessment (kappa value 0.812, AUC 0.898). The overall accuracy in evaluating multiple abdominal peritoneal compartments and retroperitoneal lymph nodes reached 85.3 % and 84.5 %, respectively. A lower accuracy than 85 % was found in the assessment of diaphragm, infracolic omentum, mesentery and retroperitoneal lymph nodes but accuracy was at 90 % and higher for the evaluation of supracolic omentum, abdominal wall and visceral peritoneum (liver, spleen, small bowels, colon).

Conclusion

To the best of our knowledge, this is the largest imaging study on ovarian cancer staging done to date. In the study, ultrasound has shown high accuracy in evaluating the rectosigmoid wall infiltration. In assessing different peritoneal and retroperitoneal compartments, ultrasound was accurate and highly specific. However, similar to other modern imaging techniques, ultrasound revealed lower sensitivity, which further supported the role of comprehensive surgical staging.

Poly Cystic Ovarian Syndrome: An Updated Overview (+endometrial -ovarian -breast)



Review ARTICLE

Front. Physiol., 05 April 2016
full text version
On the other hand, there are limited data to support any association between PCOS and breast and ovarian cancer (Chittenden et al., 2009; Fauser et al., 2012).
abstract

Poly Cystic Ovarian Syndrome (PCOS) is one of the most common metabolic and reproductive disorders among women of reproductive age. Women suffering from PCOS present with a constellation of symptoms associated with menstrual dysfunction and androgen excess, which significantly impacts their quality of life. They may be at increased risk of multiple morbidities, including obesity, insulin resistance, type II diabetes mellitus, cardiovascular disease (CVD), infertility, cancer, and psychological disorders. This review summarizes what the literature has so far provided from guidelines to diagnosis of PCOS. It will also present a general overview about the morbidities associated with this disease, specifically with its more severe classic form. Finally, the review will stress on the various aspects of treatment and screening recommendations currently used in the management of this condition. 

Analysis of two topotecan treatment schedules in patients with recurrent ovarian cancer



Abstract

Two topotecan treatment schedules in patients with recurrent epithelial ovarian cancer were evaluated. Protocol A (21 days) was 1.5 mg/m2/day topotecan on days 1 through 5 of a 21-day cycle; Protocol B (weekly) 4 mg/m2 on days 1, 8, and 15 of a 28-day cycle. Efficacy was determined by clinical exam, CT scan, and CA125 levels. Forty-three patients on Protocol A and 21 on Protocol B were evaluated. As second-line treatment, Protocol A response was 9/20 (45%). Response to Protocol B was 4/17 (23.5%; NS). As third line or more, the response on Protocols A and B together was only 3/27 (11%). High-grade haematological toxicity was reported in 12/43 (27.9%) on Protocol A and 1/21 (4.8%) on Protocol B (p = 0.04). There was no difference in progression-free-intervals between schedules in second-line treatment. The weekly protocol had lower severe haematological toxicity. Clinical response in third line or more was very low.

Marijuana Benefits, Risks for Patients With Cancer Need More Study



science news

Evidence Showing That Tumors Can Grow Without Angiogenesis and Can Switch Between Angiogenic and Nonangiogenic Phenotypes



open access
 
....All these results have therefore established the study of non-angiogenic tumors as a new field in cancer biology, but so far we have only just scratched the surface. So what now are the most pressing questions we face? 

One is: what is the biology underlying the non-angiogenic phenotype, and what are the mechanisms that allow a cancer cell to switch between angiogenic and non-angiogenic phenotypes? 

Second, how do the cancer cells interact with and co-opt the pre-existing vessels? Data published so far suggests that this is an active process (26,29). Moreover, how does this process change in different organs? 

Third, does vessel co-option also facilitate resistance to other classes of anti-angiogenic drugs, such as the VEGF-neutralizing antibody bevacizumab?
Fourth, given that vessel co-option occurs in many human cancers, including some of the most prevalent (eg, malignancies from breast, colon, rectum, and lung), is vessel co-option also a mechanism of resistance to anti-angiogenic therapy in humans and not just in animal models? 

Last, but not least, can vessel co-option be inhibited with drugs? The data of Kuczynski and colleagues shows that the response to sorafenib in HCC might be more durable if sorafenib were to be combined with a drug that targets vessel co-option. However, there are currently no drugs designed to target vessel co-option in humans. In our opinion, this represents a major deficiency in the current portfolio of oncology drugs and needs to be addressed urgently. 

Hopefully, this new field of cancer biology will lead to novel therapeutic interventions designed according to the relationship observed between neoplastic cells and vessels in tumor lesions, in the knowledge that tumors can also grow without inducing angiogenesis.

Health Tempted to follow that celebrity health trend? Check with this guy first



Tim Caulfield (lawyer) on a mission to debunk celebrity health advice

PALB2: research reaching to clinical outcomes for women with breast cancer (note: BRCA2)



Full Text

Abstract:  PALB2 has taken its place with bona fide breast cancer susceptibility genes. It is now well established that women who carry loss-of-function mutations in the PALB2 gene are at similarly elevated breast cancer risks to those who carry mutations in BRCA2. Information about PALB2 is now being used in breast cancer clinical genetics practice and is routinely included in breast cancer predisposition gene panel tests. Tens of thousands of women worldwide have now had genetic tests for PALB2 mutations in the context of breast cancer susceptibility. However, prospective data related to the clinical outcomes of PALB2 mutation carriers is lacking and very little information (beyond mutation penetrance) is available to guide current clinical management for carriers (affected and unaffected by cancer). In addition, clinical classification of the vast array of non-loss-of-function genetic variants identified in PALB2 is in its infancy. These are key areas of current research efforts and are important foundations on which to move information about PALB2 into the precision public health arena......

Media coverage of celebrities with breast cancer influencing rise in double mastectomy: Study



Medical news

 Media coverage of celebrities with breast cancer influencing rise in double mastectomy

Study finds unbalanced coverage of double mastectomy, often with no context

Evaluation of rucaparib and companion diagnostics in the PARP inhibitor landscape for recurrent ovarian cancer therapy



abstract

Drug Evaluation

Rucaparib camsylate (CO-338; 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6H-azepino[5,4,3-cd]indol-6-one ((1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)methanesulfonic acid salt) is a PARP1, 2 and 3 inhibitor. Phase I studies identified a recommended Phase II dose of 600 mg orally twice daily. ARIEL2 Part 1 established a tumor genomic profiling test for homologous recombination loss of heterozygosity quantification using a next-generation sequencing companion diagnostic (CDx). Rucaparib received US FDA Breakthrough Therapy designation for treatment of platinum-sensitive BRCA-mutated advanced ovarian cancer patients who received greater than two lines of platinum-based therapy. Comparable to rucaparib development, other PARP inhibitors, such as olaparib, niraparib, veliparib and talazoparib, are developing CDx tests for targeted therapy. PARP inhibitor clinical trials and CDx assays are discussed in this review, as are potential PARP inhibitor combination therapies and likely resistance mechanisms.

(retry) AACR (abstracts/presentations): search term by organ - gynecologic cancers: ovarian



Results matching the search 1-100 of 107
Session Search Results
Browse Details Late-Breaking Research: Tumor Biology 1 
Section 11
Browse Details Combination Chemotherapy 
Section 15
Browse Details Human in Mouse Models 
Section 29
Browse Details Targeting the Microenvironment 
Section 33
Browse Details Systems Biology 
Section 34
Browse Details Biomarkers 
Section 20
Browse Details Genomic Profiling of Cancers 
Section 5
Browse Details Late-Breaking Research: Molecular and Cellular Biology 1 
Section 10
Browse Details Altered Glucose Metabolism in Cancer 
Section 2
Browse Details Pro-Tumorigenic Microenvironment 
Section 32
Browse Details Biomarkers for Genitourinary and Gynecological Cancers 
Section 21
Browse Details Biomarkers for Melanoma and Uncommon Cancers 
Section 22
Browse Details Mechanisms of Drug Resistance 1 
Section 16
Browse Details Novel Antitumor Agents 
Section 17
Browse Details Genes and Function and Risk 
Section 36
Browse Details Genomic Analysis of Cancers 
Section 4

2016 BRCA Congress (Montreal) May 10-13th International speakers/presentations



2016 BRCA Congress (conference notice)

registration info (patients not welcome?)
  

Registration Fees:


Before Jan. 31, 2016 After Jan. 31, 2016 After April 22, 2016
Full Symposium – Physician, Pharmacist $660 CAN $775 CAN $925 CAN
Full Symposium – Genetic Counsellor / Nurse $505 CAN $595 CAN $715 CAN
Full Symposium – Post Doc. / Resident1 $480 CAN $570 CAN $680 CAN
Full Symposium – Student2 $360 CAN $420 CAN $505 CAN




Individual Days – Physician, Pharmacist $390 CAN $415 CAN $450 CAN
Individual Days – Genetic Counsellor / Nurse $290 CAN $315 CAN $345 CAN
Individual Days - Post Doc. / Resident $280 CAN $315 CAN $345 CAN
Individual Days – Student2 $210 CAN $230 CAN $250 CAN
1 Please provide proof of Post Doc / Resident status, i.e. letter from your programme director.
2 Please provide proof of full-time student status, i.e. copy of current student card or letter from your programme director.

Tuesday, April 19, 2016

ACS Updates Guidelines Regarding Overlapping Surgeries



Overlapping Surgeries

 Medscape April 18, 2016
In light of news reports questioning the practice of one surgeon performing in two surgeries scheduled at the same time, the American College of Surgeons (ACS) has updated its guidelines to clarify when this may be appropriate and what patients should know before consent.
The guidelines are part of a larger document called Statements on Principles, revised by ACS April 12.....

 The guidelines state: "A primary attending surgeon's involvement in concurrent or simultaneous surgeries on two different patients in two different rooms is not appropriate."
But "overlapping" surgeries are different, they say, and may be appropriate; for instance, if "key or critical elements" of the first operation are finished, freeing up the primary attending to start an operation in another room while others finish the first operation.

Dr. Steven Narod - Canadian Scholar award Killlam Laureates



 Lauréats Killam Laureates

Steven Narod

 April 18, 2016 | News Release
Accomplished Canadian scholars awarded over $1 million


Steven Narod is a world-leader in the field of breast and ovarian cancer. Over the course of his career, he has profoundly shaped our knowledge of how to assess risk for breast and ovarian cancer and how to reduce mortality among women who have BRCA1 and BRCA2 mutations. He studies various aspects of cancer genetics, including prevention, screening and treatment. Narod has identified founder mutations in a number of ethnic populations, including people of French-Canadian, Bahamian and Ashkenazi Jewish descent. His database of over 15,000 women with mutations from 30 countries supports numerous international collaborations. He had has a leadership role in cancer genetics studies in North America, Asia, Europe, the Caribbean and Latin America. Of particular importance was documenting the role of preventive oophorectomy on reducing death from breast and ovarian cancer.
His current studies focus on chemoprevention and MRI surveillance as an alternative to preventive surgeries as a means of reducing breast cancer risk and mortality.
"I told the research team the day we got the results that this will be on the front pages of newspapers." - Steven Narod
In other areas, he directs a Canada-wide research program in the study of breast cancer in young women. He also studies the early stages of breast cancer, including DCIS and the natural history and treatment of ovarian cancer.
Steven Narod is a Tier I Canada Research Chair in Breast Cancer, a professor in the Dalla Lana School of Public Health and the Department of Medicine at the University of Toronto and a senior scientist at Women’s College Research Institute, where he directs the Familial Breast Cancer Research Unit.
With more than 700 peer-reviewed publications and an h-index of 99,  Narod is one of the most highly cited cancer researchers in the world. In 2012, Narod was elected as a Fellow of the Royal Society of Canada.

Windfall for cancer research sets off a scramble for clout (Moonshot) - great graph/ribbons



health news
 https://www.statnews.com/wp-content/uploads/2016/04/Cancer_Run-1024x576.gif
 It was a case study in influence, and perhaps a testament of what’s to come: a major scramble for attention and clout among cancer advocacy groups.
  But if the history of cancer politics in Washington is any guide, the competition will be intense.

Theranos Is Subject of Criminal Probe by U.S. (media)



WSJ

Coping With Pain Severity, Distress, and Consequences in Women With Ovarian Cancer



abstract

BACKGROUND:

Self-regulation can be useful in understanding pain management efforts in women with ovarian cancer. Self-regulation is a parallel process of problem- and emotion-focused coping; problem-focused coping involves efforts aimed at solving/reducing the problem directly, whereas emotion-focused coping is aimed at managing negative emotions.

OBJECTIVES:

The aims of this study were to describe the types of problem- and emotion-focused coping strategies used to manage pain severity, distress, and consequences and to evaluate whether there was evidence of parallel processing (ie, use of a combination of both problem- and emotion-focused strategies).

METHODS:

Women (n = 162) from a cross-sectional study of cancer symptoms who reported pain as a most noticed symptom in the past week were included. Pearson correlations and t tests were used to evaluate relationships among the variables.

RESULTS:

Mean pain severity was 5.5 (SD, 2.7) on a 0- to 10-point scale. An average of 4.6 (SD, 2.1) coping strategies were reported. Actively manage and planning were the most frequent problem-focused strategies; relaxation was the most frequent emotion-focused strategy. Higher total number of coping strategies attempted, expressing emotions, and seeking emotional support were associated with higher pain distress and consequences scores, and actively managing pain was associated with higher pain severity.

CONCLUSION:

Women with a history of ovarian cancer continue to experience severe pain. Partial support for parallel processing was found.

IMPLICATIONS FOR PRACTICE:

The relative benefits of the 2 types of coping strategies are unclear. Thorough assessment of pain and the effectiveness of coping strategies is needed to help women identify strategies that work best for them.

Most Americans pray for healing; more than one-fourth have practiced 'laying on of hands': People pray for others' health more than for their own



science news

Summary:
Nearly nine of 10 Americans have relied upon healing prayer at some point, praying for others even more than for themselves, according to a study.

Journal Reference:
  1. Jeff Levin. Prevalence and Religious Predictors of Healing Prayer Use in the USA: Findings from the Baylor Religion Survey. Journal of Religion and Health, 2016; DOI: 10.1007/s10943-016-0240-9

Technique could help identify patients who would suffer chemo-induced heart damage



health news

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review...



open access:
Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research : Genetics in Medicine : Nature Publishing Group

Abstract

Purpose:

The extent of the responsibility of health-care professionals (HCPs) to ensure that patients’ relatives are told of their risk is unclear. Current international guidelines take confidentiality to the individual patient as the default position, but some suggest that disclosure could be default and genetic information could be conceptualized as familial.

Methods:

Our systematic review and synthesis of 17 studies explored the attitudes of HCPs, patients, and the public regarding the extent of HCPs’ responsibility to relatives with respect to disclosure.

 Discussion
This synthesis provides insight into perspectives on HCPs’ responsibility to patients’ relatives and HCP disclosure. HCPs generally felt responsible for relatives but perceived several obstacles to acting on this responsibility. The public and patients regarded HCP disclosure as unfavorable in approximately half the studies. In six competing and overlapping arguments, participants discussed the harms and benefits of disclosure by HCPs (summarized in Figure 2). Most arguments were drawn from HCP studies: public/patient views were underexplored. Limitations of the reviewed studies (including heterogeneity in populations and use of hypothetical scenarios) make our synthesis tentative, and its findings are in need of further consideration and research. Therefore, we turn to the wider literature to examine barriers to disclosure that HCPs might overcome and which arguments need more interrogation.

Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations



open access:
Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations : Genetics in Medicine : Nature Publishing Group 
 
In conclusion, the results of this systematic review indicate that, although BRCA1/2 population-based screening is currently an inefficient use of health-care resources, population-based screening of the AJ (Ashkenazi Jews) community appears to be a good value for the money. Furthermore, it is highly likely that FH (family history)-based screening will prove cost-effective, although further economic evaluations that include the costs of identifying high-risk women are needed to fully justify this conclusion. This point is crucial because counseling strategies to detect at-risk individuals could involve primary-care physicians, and currently physicians seem to be not yet adequately prepared about hereditary breast cancer and BRCA1/2 testing.47,48 Finally, in contrast to genetic testing for hereditary colorectal cancer (i.e., Lynch syndrome),49,50,51 there is no evidence for the cost-effectiveness of screening for BRCA1/2 of newly diagnosed cases of breast and ovarian cancers, followed by cascade testing of relatives. However, cancer-based genetic screening programs for BRCA1/2 that includes tools for identifying women at higher risk for inherited forms are very promising in terms of cost-effectiveness. On the contrary, more high-quality studies are needed to prove the cost-effectiveness of BRCA genetic testing as an instrument of secondary prevention in affected women with predisposing gene mutation.
In any case, the price of BRCA1/2 testing is of paramount importance in determining the cost-effectiveness of BRCA1/2 testing programs.44 If the cost of testing falls significantly, then all BRCA1/2 testing strategies analyzed in this review—perhaps including population-based screening—are likely to become highly cost-effective interventions.

Ovarian Cancer National Alliance (U.S. FDA re: safe and reliable test results)



Ovarian Cancer National Alliance

 Take Action and let Congress know you want safe and reliable test results!

Report language nestled in a House Appropriations bill up for vote in committee this week would delay the Food and Drug Administration (FDA) from finalizing guidance to regulate laboratory developed tests (LDTs). The FDA's proposed guidance would ensure that LDTs are safe, accurate and reliable. A laboratory developed test is anything from a BRCA genetic test, to a CA-125 blood test. Click here to take action now.

Why is it important to have the FDA regulate LDTs?
These tests are increasingly used to guide complex medical treatment decisions. The consequences of inaccurate test results, such as false positives, can result in the unnecessary removal of a woman's ovaries. It is critical that patients know their test results can be trusted.....

Cochrane and conflict of interest



Cochrane Community
 
David Tovey is the Editor in Chief of the Cochrane Library, and has been working with the Cochrane Editorial Unit (CEU) and the wider Cochrane collaboration in this role since 2009. In this post, he discusses Cochrane's conflict of interest policy and recent calls for re-assessment of its application in the conduct of Cochrane Reviews.
I didn’t know Bill Silverman, so I can’t judge whether he would be “a-mouldering in his grave”. However, I recognise that James Coyne has set down a challenge to Cochrane to explain its approach to commercial and academic conflicts of interest and also to respond to criticisms made in relation to the appraisal of the much debated PACE study.


Cochrane is still fairly unusual within the journal world in that it specifies that in some cases declaration of interests is necessary but insufficient, and that there are individuals or groups of researchers who are not permitted to proceed with a given systematic review. This has been true since 2004, when Cochrane’s Steering Group ratified a commercial sponsorship policy that described circumstances where authorship as proposed within a review could not go ahead. At the time, Cochrane also introduced the post of Funding Arbiter, reporting directly to its Steering Group, to ensure that the policy was followed, and to rule on ambiguous or disputed cases. As Professor Lisa Bero says “The Cochrane policy is strict because, first, there are no journals that prohibit publication of systematic reviews funded by a company with a financial interest in the outcome of the review. Second, to my knowledge, there are no journals that require the majority of authors to be without personal conflicts of interest, prohibit the first author from having a conflict of interest, or prohibit company employees with a conflict of interest from being an author. For example, the BMJ conflict of interest policy states, ‘We are not aiming to eradicate such interests; they are almost inevitable’ and authors with conflicts of interest are not prohibited from being authors of BMJ original research, systematic reviews or meta-analysis articles. The BMJ does prohibit authors with COI from being authors of: Editorials and education articles (clinical reviews, practice articles, state of the art reviews, Minerva pictures, and Endgames), but these are different from systematic reviews.”...

Monday, April 18, 2016

Research output and the public health burden of cancer: is there any relationship? U.S. & Canada



Blogger's Note:  although ovarian cancer data is not included - interesting (but not surprising)

Current Oncology (open access-register first)

....our publication results are restricted to Canada and the United States, and therefore our results might not be generalizable to other parts of the world.
-----------------------------------------------------------------------------------------------
(My) Blogger's Key Points:
Although our study does not establish a causal relationship, those data suggest a significant disconnect between the public health burden from various cancers and the relative research intensity.
 Here, we evaluated whether clinical cancer research output (total publications and number of clinical trials) is proportional to the public health burden (measured by mortality) for 10 major cancers in Canada and the United States. We also explored the relationship between research funding and research output.
 Although the volume of scientific publications is often used as a metric for research productivity, the extent to which volume correlates with improvements in human health is not known. Furthermore, the use of a journal’s impact factor as an indicator of research quality has critical limitations4,14,15.
.... When adjusting for years of life lost, they found that breast cancer and leukemia received a relatively higher degree of funding and that lung cancer was underfunded. They modelled disease burden using years of life lost and mortality, and concluded that both measures provide valuable insight into the population burden of cancer and should be considered in the allocation of cancer research funding. Building on that work, Carter and Nguyen evaluated funding allocations by the U.S. National Cancer Institute11. They found considerable mismatch between funding levels and disease burden. Breast cancer, prostate cancer, and leukemia were funded at levels higher than their relative burden, while bladder, esophagus, liver, oral, pancreatic, and uterine cancers were relatively underfunded.
 Breast cancer and prostate cancer received $73,036,061 and $36,297,058 (Canada) in research funding respectively—about 8 times and 4 times the amount that would be proportional to their corresponding cancer mortality.
---------------------------------------------------------------------------------------------

ABSTRACT

Purpose

The relative distribution of research output across cancer sites is not well described. Here, we evaluate whether the volume of published research is proportional to the public health burden of individual cancers. We also explore whether research output is proportional to research funding.

Methods

Statistics from the Canadian and American cancer societies were used to identify the top ten causes of cancer death in 2013. All journal articles and clinical trials published in 2013 by Canadian or U.S. authors for those cancers were identified. Total research funding in Canada by cancer site was obtained from the Canadian Cancer Research Alliance. Descriptive statistics and Pearson correlation coefficients were used to describe the relationship between research output, cancer mortality, and research funding.

Results

We identified 19,361 publications and 2661 clinical trials. The proportion of publications and clinical trials was substantially lower than the proportion of deaths for lung (41% deaths, 15% publications, 16% clinical trials), colorectal (14%, 7%, 6%), pancreatic (10%, 7%, 5%), and gastroesophageal (7%, 5%, 3%) cancers. Conversely, research output was substantially greater than the proportion of deaths for breast cancer (10% deaths, 29% publications, 30% clinical trials) and prostate cancer (8%, 15%, 17%). We observed a stronger correlation between research output and funding (publications r = 0.894, p < 0.001; clinical trials r = 0.923, p < 0.001) than between research output and cancer mortality (r = 0.363, p = 0.303; r = 0.340, p = 0.337).

Conclusions

Research output is not well correlated with the public health burden of individual cancers, but is correlated with the relative level of research funding.

INTRODUCTION

....Relative to other diseases, oncology has greater relative funding and a disproportionate representation in higher-impact medical journals6. However, within oncology, the number of publications4,6, clinical trials7, and research funding811 might not be distributed across cancer sites relative to the burden of disease. To our knowledge, no published study has described the interrelationships of disease burden, research output, and research funding within oncology. For the present study, we evaluated whether the volume of published cancer research is proportional to the public health burden by cancer site. We also explored whether research output is proportional to research funding by cancer site. We hypothesized that cancer research output (total publications and clinical trials) does not reflect the relative mortality for the various disease sites, but is more reflective of available research funding......

 Identifying Cancers with the Greatest Public Health Burden
Using 2013 statistics from the Canadian Cancer Society and the American Cancer Society, we identified the cancers responsible for the greatest number of deaths in Canada and the United States2,12. A priori, we excluded non-Hodgkin lymphoma, leukemia, and liver or intrahepatic biliary cancer from our study because those malignancies have multiple subtypes, and we did not feel that our bibliometric search would accurately identify related research output. Thus, the top 10 cancers, by mortality, considered here are lung, colorectal, breast, prostate, pancreatic, bladder, gastroesophageal, melanoma, kidney, and uterine cancers.

Special Supplement (Current-Oncology) - Use of Cannabinoids in Cancer Care



Vol 23 (2016) (open access - requires registration only)

Use of Cannabinoids in Cancer Care

Publication of this supplement was made possible through an unrestricted grant from Mettrum to the Canadian Consortium for the Investigation of Cannabinoids (CCIC). We sincerely thank Mettrum for their support of this project and for their ongoing commitment to research and education in cannabinoid medicine.

Table of Contents

Editorial(s)

Cancer Narratives: Words Beyond Disease

Original Article(s)

Integrative Oncology

D.I. Abrams
S8-S14

Pediatric Oncology

T. Fisher, H. Golan, G. Schiby, S. PriChen, R. Smoum, I. Moshe, N. Peshes-Yaloz, A. Castiel, D. Waldman, R. Gallily, R. Mechoulam, A. Toren
S15-S22

Review Article(s)

G. Velasco, C. Sánchez, M. Guzmán
S23-S32

Commentary(ies)

Document: OCRFA Statement on Results of GOG 252



Document: OCRFA Statement on Results of GOG 252
 

2016-04-11 | Ovarian Cancer National Alliance
 
Many members of the ovarian cancer community have been concerned about the results of GOG 252 clinical trial, which were released last month at the Society of Gynecologic Oncology’s Annual Meeting on Women’s Cancer. OCRFA consulted with a team of our scientific experts, and the consensus of the group is that the results of this trial do not mean that patients and doctors should abandon IP chemotherapy at this time.
GOG 252 is a phase III clinical trial of bevacizumab with intravenous (IV) vs. intraperitoneal (IP) chemotherapy for ovarian, fallopian tube, and peritoneal carcinoma. The results, presented in March, showed median progression-free survival (PFS) of approximately 27 to 29 months in patients with optimal stage II-III disease treated with regimens consisting of different combinations of IV and IP cisplatin, carboplatin, and paclitaxel, in combination with bevacizumab. An analysis limited to patients with optimal stage III tumors and no gross residual disease produced median PFS values of 31 to 34 months.
These results were surprising, and in contrast to the results of the decade-old GOG 172 trial, which also compared IP and IV chemotherapy regimens in ovarian cancer. GOG 172 produced a median PFS of 23.8 months with IP cisplatin, but more notably, a PFS of 60.4 months in patients who had no visible residual disease after surgery.
The recent results, which were in such stark contrast to the previous result, have left both patients and doctors alike scratching their heads....

NCI opens online platform to submit ideas about research for Cancer Moonshot (includes the public)



Cancer Moonshot 

Monday, April 18, 2016

The National Cancer Institute (NCI), part of the National Institutes of Health has launched an online platform to enable the research community and the public to submit ideas on the National Cancer Moonshot efforts. Submissions will be considered by the Blue Ribbon Panel (BRP) of scientific experts and patient advocates as they develop the scientific direction at NCI for the initiative. 
The announcement of this online platform coincides with the opening of the American Association for Cancer Research (AACR) Annual Meeting in New Orleans. Ideas for advancing progress against cancer may be submitted at CancerResearchIdeas.cancer.gov.....
 
The feedback platform is just one way in which the public can provide ideas for accelerating progress in the fight against cancer through this initiative. Ideas can also be submitted by email (link sends e-mail), or by calling the Cancer Information Service at 1-800-4-CANCER.
To sign up for updates on the online platform and other aspects of the National Cancer Moonshot Initiative, please visit the initiative’s main website.

secure blogs



Coming in Late April!
All visitors will be able to view your Blogspot domain blogs over an encrypted connection by visiting https://<your-blog>.blogspot.com. Existing links and bookmarks to your blogs will continue to work. As part of this change, the HTTPS Availability setting will go away, and your blogs will always have an HTTPS version.

Report identifies considerations for alternative payment models for cancer care (U.S.)



medical news (U.S.)


...In July 2015, the Turning the Tide Against Cancer initiative convened a roundtable to discuss the effects of APMs on oncology innovation and patient care. The participants included physicians, researchers, advocates, representatives of insurers and pharmaceutical companies, and policymakers. The group identified five issues for the future design and implementation of APMs:
  • APMs should keep pace with rapidly emerging science by incentivizing the adoption of innovative medicines and technologies that have the potential to improve patient outcomes and make health care more efficient.
  • APMs should include mechanisms to encourage patient participation as appropriate in clinical trials as well as ongoing post-market clinical research.
  • Clinical pathways should be transparent and evidence-based, and updated regularly to reflect current scientific evidence and clinical advances within the overall continuum of care.
  • When providers and patients are making treatment decisions, patients should be given a clear, comprehensive picture of their treatment options, including cost information that is tailored to the specific patient's insurance coverage and treatment plan.
  • APMs should require that clinical data be aggregated and integrated into providers' workflows via electronic health records in order to support learning health care systems. Providers should have access to data that will support their shared decision-making with patients. Similarly, patients should have access to research results collected through a learning health care system.
These recommendations will be discussed in greater detail at the Annual Meeting 2016 session....

Turning the Tide Against Cancer Through Sustained Medical Innovation: The Pathway to Progress, Amy Abernethy, Edward Abrahams, Anna Barker, Ken Buetow, Randy Burkholder, William S. Dalton, Margaret Foti, Felix Frueh, Richard B. Gaynor, Marcia Kean, Zeba Khan, Tracy Lessor, J. Leonard Lichtenfeld, John Mendelsohn, and Laura van't Veer, Clinical Cancer Research, doi: 10.1158/1078-0432.CCR-13-3430, published online 12 February 2016.
Source: American Association for Cancer Research (AACR)

Poor responding gynecologic cancers get boost from genomic profiling



medical news

....As part of an ongoing clinical trial at Rutgers Cancer Institute exploring rare and poor prognosis cancers, investigators sought to identify genomic alterations in 69 patients with gynecologic cancers that were not responding to standard care. In collaboration with Foundation Medicine, Inc. of Cambridge, Massachusetts, tissue specimens were analyzed through Next Generation Sequencing technology. Study outcomes for 64 of the cases were available and showed an average 4.97 genomic alterations per tumor....
 "Through genomic profiling, we're identifying alterations that may not have otherwise been visible through standard laboratory testing.
 
Annual Meeting of the American Association for Cancer Research (AACR)
Source: Rutgers Cancer Institute of New Jersey
 

Palliative care viewed as a stigma, despite improving quality of life for cancer outpatients



medicalnews
 April 18, 2016

 "Patients with advanced cancer and their caregivers described palliative care as carrying a negative stigma associated with death and with care at the very end of life, which provoked fear and avoidance," writes Dr. Camilla Zimmermann.....
 
The term palliative care carries a stigma for patients and their caregivers, who regard it as synonymous with impending death. Education, and possibly a name change, will be necessary to be able to integrate palliative care into routine advanced cancer care, according to new research in CMAJ (Canadian Medical Association Journal).
Palliative care is designed to improve the quality of life of patients with a serious illness and their families. The World Health Organization and all major national and international cancer societies encourage early access to palliative care. Research indicates that for people with advanced cancer, early palliative care benefits both physical and mental health and can even extend life.
However, a new study found that even patients who have benefited from early palliative care feel stigmatized because they see it as being associated with the end of life......

Research: Perceptions of palliative care among patients with advanced cancer and their caregivers, Camilla Zimmermann MD PhD, Nadia Swami BSc, Monika Krzyzanowska MD MPH, Natasha Leighl MD MMSc, Anne Rydall MSc, Gary Rodin MD, Ian Tannock MD PhD, Breffni Hannon MB ChB, CMAJ, doi: 10.1503/cmaj.151171, published 18 April 2016. open access
Commentary: Palliative care: renaming as supportive care and integration into comprehensive cancer care, Anthony J. Caprio MD, CMAJ, doi: 10.1503/cmaj.160206, published 18 April 2016.(only available $$)
Podcast: Palliative care still synonymous with death despite early integration with cancer care (SoundCloud)

Mucinous ovarian cancer: A therapeutic review



abstract
 

Highlights

Mucinous epithelial ovarian cancer (mEOC) is a rare chemoresistant subtype of ovarian cancer with distinct pathology and natural history.
It can often masquerade as metastatic mucinous tumours from the gastrointestinal tract.
In contrast to high-grade serous ovarian cancer mEOC are far less defined by p53 mutations and instead commonly harbour KRAS and HER 2 mutations.
The current gold standard of 1st line platinum/taxane doublet chemotherapy, is more tailored towards HGSOC and generally ineffective for mEOC

Mucinous ovarian cancer represents approximately 3% of epithelial ovarian cancers (EOC). Despite this seemingly low prevalence, it remains a diagnostic and therapeutic conundrum that has resulted in numerous attempts to adopt novel strategies in managing this disease. Anecdotally, there has been a prevailing notion that established gold standard systemic regimens should be substituted for those utilised in cancers such as gastrointestinal (GI) malignancies; tumours that share more biological similarities than other EOC subtypes. This review summarises the plethora of small studies which have adopted this philosophy and influenced the design of the multinational GOG142 study, which was ultimately terminated due to poor accrual. To date, there is a paucity of evidence to support delivering ‘GI style’ chemotherapy for mucinous ovarian cancer over and above carboplatin-paclitaxel doublet therapy. Hence there is an urge to develop studies focused on targeted therapeutic agents driven by refined mutational analysis and conducted within the context of harmonised international collaborations.

Small Bowel Neoplasms and Polyps (note: Lynch syndrome)



abstract
  
KEYWORDS:
Adenocarcinoma; Adenoma; Carcinoid; Crohn’s disease; Familial adenomatous polyposis; Lynch syndrome; Peutz-Jeghers syndrome; Small bowel tumors
 The small intestine is a relatively privileged organ that only rarely develops malignant or even benign tumors. Given this rarity, the relative inaccessibility of the organ during routine endoscopic procedures, and the typical absence or nonspecific nature of clinical manifestations, these tumors often go undiagnosed. Treatment and prognosis are tailored to each histological subtype of tumor. This chapter will discuss the epidemiology, presentation, diagnostics, and management for the most common small bowel tumors, and will highlight the importance of recognizing patients at higher risk of small bowel neoplasia.

The marketing of mindfulness meditation



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Sunday, April 17, 2016

AACR: Broadening tumor spectrum in Lynch syndrome: increased incidence for 15 distinct cancer types (note ovarian)



OASIS

Presentation Abstract
Abstract Number: 5216
Presentation Title: Broadening tumor spectrum in Lynch syndrome: increased incidence for 15 distinct cancer types
Presentation Time: Wednesday, Apr 20, 2016, 7:30 AM -11:00 AM
Location: Section 34
Poster Board Number: 12
Author Block: Christina Therkildsen, Steen Ladelund, Lars Joachim Lindberg, Lars Smith-Hansen, Mef Nilbert. Hvidovre Hospital, Hvidovre, Denmark
Abstract Body: Introduction: Lynch syndrome is a multi-tumor syndrome predominantly associated with an increased risk of colorectal cancer, but is indeed linked to a yet uncertain number of extra-colonic tumor types.
Methods: In order to determine the risk for extra-colonic tumors in Lynch syndrome, we determined the incidence rates for 21 distinct malignancies in the national Danish Lynch syndrome cohort compared to an age-and sex matched control cohort from the Danish population.
Results: Based on data from 1494 Lynch syndrome mutation carriers, significantly increased risks were demonstrated for 15 cancer types. These included Lynch syndrome-related malignancies, such as cancer of the endometrium, the ovary, the small bowel, the urinary tract and brain tumors as well as tumor types with an undefined role in Lynch syndrome, such as breast cancer, gastric cancer, pancreatic cancer, skin cancer, prostate cancer, lung cancer, kidney cancer, and testicular cancer. Distinctive peak ages were defined with the highest incidence rate ratio at age 30-49 years for ovarian cancer and 50-69 years for endometrial cancer, breast cancer, and brain tumors to continuously increasing incidence rate ratios with increasing age for e.g. urothelial cancer, gastric cancer, pancreatic cancer and skin cancer.
Conclusion: The broad tumor spectrum in Lynch syndrome is of relevance to consider during genetic counseling, whereas the variable peak incidence ages provide a basis for precision surveillance programs that consider the different risks throughout life.

AACR Live Webcast: A Cancer Dialogue – Maximizing Cancer Cures: How Do We Get There? - YouTube



AACR Live Webcast
 

AACR Live Webcast: A Cancer Dialogue – Maximizing Cancer Cures: How Do We Get There?


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A Cancer Dialogue – Maximizing Cancer Cures: How Do We Get There?

AACR Annual Meeting 2016
Morial Convention Center
New Orleans, Louisiana

Sunday 4/17/2016
4:30 PM - 6:00 PM

OASIS - Session 5: Genomic Profiling of Cancers (sundry/posters)



OASIS


Session Title: Genomic Profiling of Cancers
Session Type: Poster Session
Session Start/End Time: Sunday, Apr 17, 2016, 1:00 PM - 5:00 PM
Location: Section 5
Session Category: Molecular and Cellular Biology / Genetics

OASIS - AACR 2016 search 'sessions' "ovarian" (total 107)



OASIS

 'Session' - Results matching the search ("ovarian") = 107


AACR 2016 search results - "ovarian" "presentations" (total 175)



OASIS - Results matching the search 1-25 of 175 (25 per page)

OASIS - search results - "ovarian" "presentations" 100 per page (out of 175 total)

OASIS - AACR 2016 Online Program Planner



OASIS 

AACR Annual Meeting 2016
Online Proceedings and Itinerary Planner

  • Presenter Index: Browse presenters and authors and view their presentations and sessions.
  • Browse: View sessions by Category, Type, or Date.
  • Itinerary: Create your personal meeting schedule and print or sync it with your mobile device.

AACR Annual Meeting 2016 (link to view abstracts etc)



AACR 

Abstracts

Regular Abstracts Now Available. The regular abstracts that have been scheduled for oral and poster presentation, as well as the titles of late-breaking and clinical trial abstracts, are now available through the online itinerary planner. The full text of most late-breaking and clinical trial abstracts will be posted to the itinerary planner on Friday, April 15. Any abstracts that are included in the press program will be posted to the itinerary planner on the date and time of their presentation at the meeting. 

Medscape Lifestyle Report 2016: Bias and Burnout (physician by specialty)



Medscape


Slide 1
This year's lifestyle report covers two important aspects of a physician's personal life that could affect treatment: burnout and bias. Over 15,800 physicians responded from over 25 specialties, providing some surprising responses relating to these issues. The survey also repeated some of last year's questions on marijuana use and prescribing to determine whether there were any changes in responses, given its legitimacy in more states. (Note: Values in chart have been rounded and may not match the sums described in the captions.)
Slide 2
This year's Medscape survey, echoing other recent national surveys,[1,2] strongly suggests that burnout among US physicians has reached a critical level. Burnout in these surveys is defined as loss of enthusiasm for work, feelings of cynicism, and a low sense of personal accomplishment. In this year's Medscape report, the highest percentages of burnout occurred in critical care, urology, and emergency medicine, all at 55%. Family medicine and internal medicine follow closely at 54%. In last year's report, the highest percentages of burnout were also in critical care (53%) and emergency medicine (52%). Of note, however, burnout rates for all specialties are higher this year. The 2015 survey published in the Mayo Clinic Proceedings[1] compared burnout between 2011 and 2014 and observed an increase in the percentage of physicians reporting at least one burnout symptom, from 45.5% to 54.4%.

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#aacr16 hashtag on Twitter



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