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Saturday, March 05, 2016

10 yr Review: The application and outcome of standard of care treatment in elderly women with ovarian cancer



Blogger's Note: 'elderly' as defined 65 yrs+

When comparing the elderly (65-74 years) with the very elderly
98 (≥75 years), increased age was also associated with advanced stage and higher grade [12].

open access (provisional pdf)
The application and outcome of standard of care treatment in elderly women with ovarian cancer: a literature review over the last 10 years.


The rising number and increasing longevity of the elderly population calls for improvements and potentially a more personalized approach to the treatment of cancer in this group. Elderly patients frequently present with a number of comorbidities, complicating surgery and chemotherapy tolerability. In the case of ovarian cancer, elderly women present with more advanced disease, making the issue of providing adequate treatment without significant morbidity critical. Most studies support the application of standard of care treatment to elderly women with ovarian cancer, yet it seems to be offered less frequently in the elderly. The objective of this review is to examine the application and outcome of standard of care treatment in elderly women with ovarian cancer. The aim is to ultimately improve the approach to treatment in this group.

Received: 01 Dec 2015; Accepted: 04 Mar 2016.
Edited by:
Nicolas Wentzensen, National Cancer Institute, USA

Disparities in Gynecological Malignancies



open access

Introduction

The Institute of Medicine released a landmark report in 2003 titled “Unequal Treatment: Confronting Racial and Ethnic Disparities in Health Care,” which demonstrated disparities in the U.S. health care system between treatment of racial and ethnic minorities and Whites, subsequently resulting in poorer health outcomes for millions of Americans (1).
Since that time, the National Cancer Institute (NCI) through the Center to Reduce Cancer Health Disparities (CRCHD), the American Cancer Society, the American Society of Clinical Oncology, and the Society of Gynecologic Oncology has committed to the goals of eliminating disparities in cancer-related outcomes (24). The NCI defines cancer health disparities as “differences in the incidence, prevalence, mortality, and burden of cancer and adverse related conditions that exist among specific population groups in the United States (2).”.....

Geographic Access and Hospital-Based Discrepancies

Research-Based Discrepancies

Socioeconomic Status and Health Insurance Status

Race

 Ovarian Cancer

Epithelial ovarian cancer (EOC) is the fifth cause of cancer death among women in the United States, accounting for an estimated 21,290 new cases and 14,180 cancer deaths in the US in 2015 (31). With aggressive surgical and chemotherapeutic management, overall survival has improved from 36% during the period of 1975–1977 to 45% during the period 2004–2010 (p < 0.05). However, the survival rate over the same time period for Black women has actually decreased from 42 to 36% (46). From 2002 to 2011, the mortality rate associated with ovarian cancer decreased significantly by 2% per year among White women, 1.4% per year among Hispanic women, but remained unchanged among Black women (47).

Hospital Variation in the Practice of Bilateral Salpingectomy With Ovarian Conservation in 2012



abstract
 

OBJECTIVE:

To examine hospital variation in the practice of bilateral salpingectomy with ovarian conservation at the time of benign hysterectomy.

METHODS:

We conducted a cross-sectional study using data from the 2012 National Inpatient Sample. We identified hospitalizations for benign, nonobstetric hysterectomy in adult women and excluded women who had elevated risk for ovarian cancer or a subsequent operation of the ovary. Of the remaining sample, we calculated the rate of bilateral salpingectomy with ovarian conservation for each hospital and conducted multivariable regression analysis to identify factors associated with a hospital's practice of this procedure.

RESULTS:

There were 63,306 hospitalizations for hysterectomy, and 20,635 were for adult women at low risk for ovarian cancer or subsequent ovarian surgery. Among these low-risk women, only 5.9% (95% confidence interval 5.4-6.5%) received bilateral salpingectomy with ovarian conservation. The rate varied markedly across 744 hospitals in the United States ranging from 0% to 72.2%. At 376 of the hospitals (50.5%), no low-risk women received bilateral salpingectomy with ovarian conservation. When categorizing hospitals into tertiles based on the proportion of their hysterectomies performed laparoscopically, hospitals in the highest tertile were more likely to have low-risk patients undergoing bilateral salpingectomy with ovarian conservation than those in the lowest tertile (adjusted odds ratio 2.343, P=.02). Geographic region, hysterectomy volume, and proportion of white patients were also significantly associated with a hospital's likelihood of having low-risk patients undergoing this procedure.

CONCLUSION:

The rate of bilateral salpingectomy with ovarian conservation was low in low-risk women undergoing benign hysterectomies. Hospitals varied widely in their practice.

New Approaches for Immune Directed Treatment for Ovarian Cancer



abstract

 Opinion statement

The immune system plays an active role in the pathogenesis of ovarian cancer (OC), as well as in the mechanisms of disease progression and overall survival (OS). Immunotherapy in gynecological cancers could help to revert immunosuppression and lymphocyte depletion due to prior treatments. Current immunotherapies for ovarian cancer, like all cancer immunotherapy, are based on either stimulating the immune system or reverting immune suppression. Several approaches have been used, including therapeutic vaccines, monoclonal antibodies; checkpoint inhibitors and adoptive T cell transfer. Most of these therapies are still in early-phase testing (phase I and II) for ovarian cancer, but the initial data in ovarian cancer and successful use in other types of cancers suggests some of these approaches may ultimately prove useful for ovarian cancer as well. Ovarian cancer vaccines have shown only a modest benefit in ovarian cancer when used as monotherapy, but these agents may be able to enhance antitumor activity when combined with chemotherapy, checkpoint inhibitors, or other immunotherapies. Monoclonal antibodies have been explored in ovarian cancer but despite encouraging phase II data, randomized studies failed to demonstrate significant clinical benefit. Check point inhibitors have promising activity in several solid tumors and have demonstrated a favorable toxicity profile. Data from early clinical trials utilizing PD1 and PD-L1 inhibitors showed encouraging results. Ongoing clinical trials are evaluating the role of check point inhibitors in combination with chemotherapy. Adoptive T cell transfer involves the infusion of ex vivo activated and expanded tumor specific T cells, using various sources and types of T cells. While this approach has been explored in several hematologic malignancies, it constitutes early research in ovarian cancer. Immunotherapy remains investigational in ovarian cancer and the benefit of this approach in improving progression-free survival (PFS) or OS is unknown. Previous clinical trials have not selected patients based on biomarkers and this may explain the negative results. We expect to discover that tumor response will relate to the patient’s immune features and specific tumor characteristics. We are only beginning to realize the potential of immunotherapy for ovarian cancer patients, and one goal of future clinical trials will be to identify subsets of patient based on histologic, molecular, and immune characteristics.

Impact of molecular profiling on overall survival of patients with advanced ovarian cancer



open access
 
Impact of molecular profiling on overall survival of patients with advanced ovarian cancer
PDF |  HTML
 
DOI: 10.18632/oncotarget.7835

Thomas J. Herzog1,*, David Spetzler2, Nick Xiao2, Ken Burnett2, Todd Maney2, Andreas Voss2, Sandeep Reddy2, Robert Burger3, Thomas Krivak4, Matthew Powell5, Michael Friedlander6, William McGuire7
1 University of Cincinnati Cancer Institute, Cincinnati, OH, USA
2 Caris Life Sciences, Phoenix, AZ, USA
3 University of Pennsylvania, Philadelphia, PA, USA
4 Western Pennsylvania Gynecological Oncology, Mars, PA, USA
5 Washington University School of Medicine, St. Louis, MO, USA
6 Prince of Wales Hospital, Sydney, Australia,
7 VCU Massey Cancer Center, Richmond, VA, USA

Published: March 01, 2016
 
                        Patient characteristics
There were 241 EOC patients with advanced stage cancers who underwent treatment and had at least 9 months of follow-up data, diagnostic staging of at least IIIC or having metastasis or treatments prior to profiling. Of 241 eligible patients, 17 were excluded because they received no drugs after the time of tissue collection or the drugs they received were not classified by the molecular profile (received no drugs of predicted benefit or lack-of-benefit; Figure 1).
In conclusion, this report suggests a potential predictive role of molecular profiling to avoid use of inactive therapies. Additionally, a prognostic biomarker-derived phenotype was identified that demonstrated particularly inferior OS. The conclusions generated here, while intriguing, will need to be validated in an additional prospective observational study with much larger patient numbers. 

Better Training for Menopausal Management Urgently Needed (misuse of WHI data)



Medscape
 
 The American College of Obstetricians and Gynecologists published an updated committee opinion this month addressing this issue.
....Dr Montgomery agrees that the WHI findings have not been appropriately communicated to providers and women.
"Medical educators have remained fixed in time since the WHI came out saying estrogen kills, but if they kept up with the literature, estrogen keeps women alive longer," Dr Montgomery said. "Young doctors are being told hormones are terrible and don't prescribe them, but if you look at the data, they actually save lives."....
            Misunderstanding of Women's Health Initiative Results
One stumbling block to quality care of perimenopausal women, write Dr Manson and Dr Kaunitz, is the misuse of the initial findings of the Women's Health Initiative (WHI) trial, which has led to "anxiety and confusion" in women who now fear hormone therapy.

Statement: of the AGO Kommission Ovar (et al) Regarding the Use of (HIPEC) in Ovarian Cancer



open access - pdf

Statement of the AGO Kommission Ovar, AGO Study Group, NOGGO,
AGO Austria and AGO Switzerland Regarding the Use of Hyperthermic
Intraperitoneal Chemotherapy (HIPEC) in Ovarian Cancer
 
 The AGO Kommission Ovar already published a statement in 2013, warning about the uncritical use of hyperthermic intraperitoneal chemotherapy (HIPEC) outside controlled studies. This statement has now been updated after the most recent literature was reviewed by AGO Kommission Ovar, the AGO Study Group, NOGGO, AGO Austria and AGO Switzerland. The authors conclude that HIPEC remains experimental. Its use is not recommended and should be rejected outside of prospective controlled trials.


 

Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer



abstract (Journal of Medical Genetics)

Purpose To characterise the prevalence of pathogenic germline mutations in BRCA1 and BRCA2 in families with breast cancer (BC) and ovarian cancer (OC) history.
Patients and methods Data from 21 401 families were gathered between 1996 and 2014 in a clinical setting in the German Consortium for Hereditary Breast and Ovarian Cancer, comprising full pedigrees with cancer status of all individual members at the time of first counselling, and BRCA1/2 mutation status of the index patient.
Results The overall BRCA1/2 mutation prevalence was 24.0% (95% CI 23.4% to 24.6%). Highest mutation frequencies were observed in families with at least two OCs (41.9%..) and families with at least one breast and one OC (41.6%..), followed by male BC with at least one female BC or OC (35.8%..). In families with a single case of early BC (<36 years), mutations were found in 13.7% .. Postmenopausal unilateral or bilateral BC did not increase the probability of mutation detection. Occurrence of premenopausal BC and OC in the same woman led to higher mutation frequencies compared with the occurrence of these two cancers in different individuals (49.0%....to 35.2%).
Conclusions Our data provide guidance for healthcare professionals and decision-makers to identify individuals who should undergo genetic testing for hereditary breast and ovarian cancer. Moreover, it supports informed decision-making of counselees on the uptake of genetic testing.

Friday, March 04, 2016

2nd-Line IP Chemotherapy for Recurrent Epithelial Ovarian, Tubal and Peritoneal Cancer



abstract
 

BACKGROUND:

The superiority of frontline intraperitoneal (IP) over intravenous (IV) chemotherapy is well established in the treatment of epithelial ovarian cancer. However, the role of IP chemotherapy in the second-line setting has rarely been investigated.

METHODS:

Consecutive patients diagnosed with recurrent epithelial, tubal and peritoneal cancers between January 2000 and December 2012 were recruited using a propensity score-matching technique to adjust relevant risk factors.

RESULTS:

In total, 310 patients were included in the final analysis (94 for platinum-refractory/resistant disease and 216 for platinum-sensitive disease). IP chemotherapy demonstrated significantly longer median progression-free survival than IV chemotherapy (4.9 vs. 2.4 months, p < 0.001, for platinum-refractory/resistant disease, and 9.8 vs. 6.9 months, p < 0.001, for platinum-sensitive disease).

CONCLUSIONS:

Second-line IP chemotherapy confers longer progression-free survival than IV chemotherapy. Large-scale clinical trials should be conducted to validate the true efficacy.

(cochrane Review) Intraoperative frozen section analysis for the diagnosis of early stage ovarian cancer in suspicious pelvic masses



The Cochrane Library

 Plain language summary

Is a 'quick diagnosis' test on an ovarian mass during surgery accurate?

The issue
When women go to their doctor with a mass that could be ovarian cancer, they are normally referred for surgery, since the mass may need to be removed and examined microscopically in a laboratory in a procedure known as paraffin section histopathology. A third of women with ovarian cancer present with a cyst or mass without any visible evidence of spread elsewhere. However, in these apparently early-stage cancers (confined to the ovary) surgical staging is required to decide if chemotherapy is required. This staging consists of sampling tissues within the abdomen, including lymph nodes.
Different staging strategies exist. One is to perform surgical staging for all women who might have a cancer, to get information about spread. This may result in complications due to additional surgical procedures that may turn out to be unnecessary in approximately two thirds of women.
A second strategy is to perform an operation to remove just the suspicious mass and await the paraffin section diagnosis. This may result in needing a further operation in one third of women if cancer is confirmed, putting them at increased risks from another operation.
A third strategy is to send the mass to the laboratory during the operation for a quick diagnosis, known as 'frozen section'. This helps the surgeon decide if further surgical treatment is required during a single operation.
Why is this review important?
Frozen section is not as accurate as the traditional slower paraffin section examination, and it entails a risk of incorrect diagnosis, meaning that some women may not have all the samples taken at the initial surgery and may need to undergo a second operation; and others may undergo unnecessary surgical sampling.
How was this review conducted?
We searched all available studies reporting use of frozen section in women with suspicious ovarian masses. We excluded studies without an English translation and studies without enough information to allow us to analyse the data.
What are the findings?
We included 38 studies (11,181 women), reporting three types of diagnoses from the frozen section test.
1. Cancer, which occurred in an average of 29% of women.
2. Borderline tumour, which occurred in 8% of women.
3. Benign mass.
In a hypothetical group of 1000 patients where 290 have cancer and 80 have a borderline tumour, 261 women would receive a correct diagnosis of a cancer and 706 women would be correctly diagnosed without a cancer based on a frozen section result. However, 4 women would be incorrectly diagnosed as having a cancer where none existed (false positive), and 29 women with cancer would be missed and potentially need further treatment (false negative).
If surgeons used a frozen section result of either a cancer or a borderline tumour to diagnose cancer, 280 women would be correctly diagnosed with a cancer and 635 women would be correctly diagnosed without a cancer. However, 75 women would be incorrectly diagnosed as having a cancer, and 10 women with cancer would be missed on the initial test and found to have a cancer after surgery.
If the frozen section result reported the mass as benign or malignant, the final diagnosis would remain the same in, on average, 94% and 99% of the cases, respectively.
In cases where the frozen section diagnosis was a borderline tumour, there is a chance that the final diagnosis would turn out to be a cancer in, on average, 21% of women.
What does this mean?
Where the frozen section diagnosis is a borderline tumour, the diagnosis is less accurate than for benign or malignant tumours. Surgeons may choose to perform additional surgery in this group of women at the time of their initial surgery in order to reduce the need for a second operation if the final diagnosis turns out to be a cancer, as it would on average in one out of five of these women.

Sotatercept (ACE-011) for the treatment of chemotherapy-induced anemia in patients with metastatic breast cancer or advanced or metastatic solid tumors treated with platinum-based chemotherapeutic regimens



open access (pdf)

 Sotatercept (ACE-011) for the treatment of chemotherapy-induced anemia in patients with metastatic breast cancer or advanced or metastatic solid tumors treated with platinum-based chemotherapeutic regimens: results from two phase 2 studies
 
Abstract
Purpose: Sotatercept may represent a novel approach to the treatment of chemotherapy-induced anemia (CIA). We report the results from two phase 2 randomized studies examining the use of sotatercept for the treatment of CIA in patients with metastatic cancer.
 
 Conclusions
Although both studies were terminated early, these results indicate that sotatercept is active and has an ac- ceptable safety profile in the treatment of CIA

(Northern Sweden) Decentralized colonoscopic surveillance with high patient compliance prevents hereditary/familial colorectal cancer



open access (pdf)

       Northern Sweden Health Care Region. Median population 11995–2012  = 898 696

                         study: 278 individuals from 118 different families

Conclusions
Our study provides a reasonably safe strategy for surveillance of FCRC and HCRC with high patient compliance in a sparsely populated area by using decentralized colonoscopies. However, health economic analyses and modeling are needed to find the most cost effective way to prevent cancer devel- opment in individuals with a family history of CRC. These future studies of surveillance programs should include patient
compliance as an important factor and not only focus on start of surveillance and the lengths of the intervals

(Lynch syndrome) National Bubble Soccer AliveAndKickn Charity Event March 12th



Charity Event 

 

You can register here for the following locations

Chicago, IL Albany, NY Allston, MA
Atlanta, GACharlotte, NCFairfield, NJ
Houston, TX Miami, FL Raleigh/Durham/Chapel Hill, NC
San Diego, CA Silicon Valley, CA Sunnyvale, CA
Tampa Bay, FL       

Medscape: 'Surprising Gaps' in Ovarian Cancer, Says IOM Report



Medscape

 March 03, 2016 Despite advances in cancer research, there remain "surprising gaps" in the fundamental understanding of ovarian cancer, according to a report published online by the National Academies of Sciences, Engineering, and Medicine.
One of the key findings of the report is that ovarian cancer should not be categorized as a single disease; rather, it should be considered a constellation of different cancers that involve the ovary.
There are several distinct subtypes with different origins, risk factors, genetic mutations, biologic behaviors, and prognoses.
Recent evidence suggests many ovarian cancers arise outside the ovary, such as in the fallopian tubes, and eventually metastasize to the ovary, according to the report. The cancers can also arise from cells that are not considered intrinsic to the ovary.
"We are tying to understand the root causes of ovarian cancer — why some women get it and why some don't, and why some women live for decades and others don't," said Beth Karlan, MD, director of the women's cancer program at Cedars-Sinai Medical Center in Los Angeles, who is a member of the Committee on the State of the Science of Ovarian Cancer Research, which is responsible for the report.
The committee was created by the Institute of Medicine, with support from the Centers for Disease Control and Prevention.
"We now have technologies that we can embrace to help us understand the root causes from a molecular level and immunologic level," Dr Karlan said during a press briefing held to highlight key findings of the report. We also need to understand individual behavior, in terms of exercise and diet, so that we can determine where we go from here, she noted.
"We are hoping to harness this knowledge in terms of early detection, risk assessment, prevention, and treatment. It was this type of expertise and interest that brought this committee together," she explained.
One of the Deadliest Cancers
Although ovarian cancer is relatively uncommon, it is one of the deadliest cancers. Each year, more than 21,000 women are diagnosed with ovarian cancer in the United States, and more than 14,000 women die from the disease.
Late diagnosis is a major concern, said Jerome F. Strauss III, MD, executive vice president for medical affairs and dean of the Virginia Commonwealth University School of Medicine in Richmond, who is chair of the committee.
"The diagnosis is often made when the disease is disseminated, and about 60% of women who are diagnosed with ovarian cancer are diagnosed at advanced stages," said Dr Strauss, who chaired the panel at the press briefing. "It is associated with a 5-year survival of less than a 30%."
Committee Findings
The report is perhaps the most comprehensive document that has tackled the question of "where do we go from here" in ovarian cancer research,

Weekly Paclitaxel Prolongs PFS in a Subset of Ovarian Cancer Patients



medscape

 "We believe that the effect of the Avastin neutralized the effect of weekly paclitaxel," Dr. Chan told Reuters Health in a telephone interview. "If you look at the subgroup of patients who did not get (bevacizumab), weekly paclitaxel was beneficial. In fact, it had a 38% improvement in our cohort in progressive-free survival."

 (abstract) NEJM

Managing Menopause: Are the WHI Results Being Misunderstood?



Medscape


Hello. This is Dr JoAnn Manson, professor of medicine at Harvard Medical School and Brigham and Women's Hospital. I would like to talk with you about a prospective piece that I and my colleague, Dr Andrew Kaunitz, have recently published in the New England Journal of Medicine, titled "Menopause Management: Getting Clinical Care Back on Track."[1] We wrote this article to address ongoing confusion about the Women's Health Initiative (WHI) and what it did and did not address. There has been continued misunderstanding about some of the WHI findings.
The WHI was designed to address a very specific question: What is the balance of benefits and risks when menopausal hormone therapy is initiated for the express purpose of trying to prevent chronic disease in postmenopausal women across a broad range of ages, including many women in their 60s and 70s? At the time when the WHI was initiated, it was becoming an increasingly common practice to start hormone therapy in women more than a decade past menopause for the purpose of trying to prevent heart disease, cognitive decline, and many other chronic diseases.....

Majority of Americans and Canadians Expects Cancer Cure in Their Lifetime



My Healthy Today


SOURCE: Harris Poll, news release, Feb. 3, 2016
2/4/2016
THURSDAY, Feb. 4, 2016 -- A majority of American and Canadian adults believe a cure for cancer will be found in their lifetime, and that a cancer diagnosis is not a death sentence, according to a new Harris Poll.
Nearly three out of five Americans and Canadians expect a cure for cancer in their lifetime. That belief is especially strong among those ages 18 to 34. Nearly three-quarters of young Americans and 69 percent of Canadians in that age group expect a cure in their lifetime.
And, about two-thirds of Americans and Canadians don't think death is inevitable when someone is diagnosed with cancer, the poll found.

However, Americans adults under 35 are more likely to believe that a cancer diagnosis is a death sentence than those 35 and older (39 percent vs. 29 percent). Americans whose lives have been affected by cancer are also more likely to view cancer as deadly compared to those who haven't been affected by cancer (35 percent vs. 29 percent), the poll revealed.
The poll was released to mark World Cancer Day on Feb. 4. It included just over 2,000 American and more than 1,100 Canadian adults. The online survey was conducted in late January.....

March 5, 2016: Ovarian cancer screening and mortality in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS)



open access
Ovarian cancer screening and mortality in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS): a randomised controlled trial - The Lancet
  
full text

Interpretation

Although the mortality reduction was not significant in the primary analysis, we noted a significant mortality reduction with MMS when prevalent cases were excluded. We noted encouraging evidence of a mortality reduction in years 7–14, but further follow-up is needed before firm conclusions can be reached on the efficacy and cost-effectiveness of ovarian cancer screening.

March 5, 2016: Editorial - UKCTOCS and the evaluation of screening for ovarian cancer



Editorial- The Lancet
 
Ovarian cancer is the fifth most common cause of cancer-related death in women in Europe. Vague symptoms mean that most women present with advanced disease, so that 5-year survival is less than 40%. Progress in the past generation has been slow, with little added benefit from biomarkers, mechanism-based treatments, or surgical innovations. Recently, emphasis has shifted to earlier diagnosis with clinical decision aids and population screening—a challenging proposition for a disease of low prevalence and without a recognisable latent phase. Therefore, results of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS), published in today's Lancet, have been highly anticipated: if ovarian cancer can be detected earlier by screening and treated more promptly, might medicine finally gain the upper hand against this stubborn illness?
Maybe. At a median 11 years' follow-up of the 202 638 women allocated to annual screening by either transvaginal ultrasound, a multimodal combination of CA125 augmented with ultrasound, or to no screening, the primary outcome of death due to ovarian cancer was not significantly different. Further analyses suggested that there may be a late survival advantage from screening, but longer follow-up is needed.
Although full understanding of screening in ovarian cancer and its cost-effectiveness will take longer to establish, the successful conclusion of UKCTOCS represents a major achievement for clinical science in the NHS. First, it affirms the importance of science-based priority setting (the NHS Health Technology Assessment programme identified the need for such a trial in 1998). Second, it shows boldness in recognising that very large-scale, publicly funded, randomised trials are needed in some situations of equipoise—and that by asking the right question at the right time, widespread collaboration is possible. Third, it is a testimony to the trial organisation and investigators, that they achieved around 80% compliance and 99% follow-up. The philosophy that underpinned UKCTOCS is a crucial part of an integrated health service and should be applauded and fostered.

OVARIAN Institute of Medicine - Ovarian Cancer - Recommendations - EVOLVING PARADIGMS IN RESEARCH AND CARE



pdf (brief report)
 
To download the full report and to find additional resources, visit
 
Ovarian Cancers: Evolving Paradigms in Research and Care gives a broad overview of the state of the science in ovarian cancer research, highlights major knowledge gaps, and provides recommendations to help reduce the incidence of and morbidity and mortality from ovarian cancers by focusing on promising research themes that could advance risk prediction, prevention, early detection, comprehensive care, and cure. The committee focused on identifying the research gaps that, if addressed, could have the greatest impact on reducing morbidity or mortality.
The committee identified four overarching concepts that should be applied to each recommendation in this report:

• As the most common and lethal subtype, the study of high-grade serous carcinomas needs to be given priority.
• Even so, more subtype-specific research is also needed to further define the differences among the various subtypes;
• Given the relative rarity and heterogeneity of ovarian cancers, collaborative research (including the pooling and sharing of data and biospecimen resources, such as through consortia) is essential; and
• The dissemination of new knowledge and the implementation of evidence-based interventions and practices are the final steps in the knowledge translation process.

A wide variety of stakeholders are integral to ovarian cancer research, including the U.S. Congress, federal agencies (e.g., the Centers for Disease Control and Prevention, Department of Defense, Food and Drug Administration, National Institutes of Health), private foundations, industry, academic institutions, professional societies, and advocacy groups. Most of these stakeholders are engaged in research across the care continuum, and many are both funders and performers of research. The committee therefore concluded that directing research toward the gaps identified in the recommendations is the responsibility of all stakeholders in their individual and collaborative efforts to fund, perform, or advocate for ovarian cancer research.
The following recommendations are intertwined and so need to be considered simultaneously, not sequentially. Their sequence should not be considered as priority of importance or order of implementation. (11).....

Thursday, March 03, 2016

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing



abstract

 Conclusions These results suggest that truncating variants in BRIP1, and in particular p.Arg798Ter, are not associated with a substantial increase in breast cancer risk. Such observations have important implications for the reporting of results from breast cancer screening panels.

Surgical treatment pattern and outcomes in epithelial ovarian cancer patients from a cancer institute in Kerala, India



open access

 Discussion
This retrospective study was done with the aim of studying the treatment pattern and survival of advanced EOC in Indian women. We found that more patients were given NACT than primary surgery but primary surgery was associated with better outcomes within a four year follow-up period. The difference was statistically significant for Stage IIIC in optimally as well as sub-optimally debulked patients.

Hereditary non-BRCA gynaecological tumors



abstract

 Early diagnosis and proper management of gynecologic malignancies represent a challenge in modern oncology. A growing interest has arisen around the gynecological manifestations of hereditary cancer syndromes. In particular, the discovery of the BRCA1 and BRCA2 genes in ovarian cancer and the mismatch repair genes (MMR) in endometrial carcinoma has revolutionized our approach to the diagnosis and screening of women for ovarian and uterine cancers. The clinical, genetic and pathological features of hereditary cancer syndromes with gynecological manifestations are reviewed focusing on Lynch Syndrome, also known as Hereditary Nonpolyposis Colorectal Carcinoma (HNPCC), Peutz-Jeghers Syndrome, Cowden Syndrome or Multiple Hamartoma Syndrome, Gorlin Syndrome or Nevoid basal-cell carcinoma syndrome (NBCCS) and Reed's Syndrome or Hereditary leiomyomatosis and renal cell cancer (HLRCC).

Comparing the coverage, recall, and precision of searches for 120 systematic reviews in Embase, MEDLINE, and Google Scholar



open access

Background

Previously, we reported on the low recall of Google Scholar (GS) for systematic review (SR) searching. Here, we test our conclusions further in a prospective study by comparing the coverage, recall, and precision of SR search strategies previously performed in Embase, MEDLINE, and GS.

Methods

The original search results from Embase and MEDLINE and the first 1000 results of GS for librarian-mediated SR searches were recorded. Once the inclusion-exclusion process for the resulting SR was complete, search results from all three databases were screened for the SR’s included references. All three databases were then searched post hoc for included references not found in the original search results.

Results

We checked 4795 included references from 120 SRs against the original search results. Coverage of GS was high (97.2 %) but marginally lower than Embase and MEDLINE combined (97.5 %). MEDLINE on its own achieved 92.3 % coverage. Total recall of Embase/MEDLINE combined was 81.6 % for all included references, compared to GS at 72.8 % and MEDLINE alone at 72.6 %. However, only 46.4 % of the included references were among the downloadable first 1000 references in GS. When examining data for each SR, the traditional databases’ recall was better than GS, even when taking into account included references listed beyond the first 1000 search results. Finally, precision of the first 1000 references of GS is comparable to searches in Embase and MEDLINE combined.

Conclusions

Although overall coverage and recall of GS are high for many searches, the database does not achieve full coverage as some researchers found in previous research. Further, being able to view only the first 1000 records in GS severely reduces its recall percentages. If GS would enable the browsing of records beyond the first 1000, its recall would increase but not sufficiently to be used alone in SR searching. Time needed to screen results would also increase considerably. These results support our assertion that neither GS nor one of the other databases investigated, is on its own, an acceptable database to support systematic review searching.

Wednesday, March 02, 2016

IBM and New York Genome Center’s new cancer tumor repository aims to revolutionize treatment



media

 The initial project will begin with 200 patients being treated at New York City-area hospitals, such as Memorial Sloan Kettering and Columbia-Presbyterian. Recruitment of patients begins immediately and is focusing on the neediest patients who have not responded to multiple treatments.

Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant (BRCA1/2/Ashkenazi Jewish...)



Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant
 

Discussion

We performed WGS of multiple primary cancers and identified a novel germline PALB2 structural variant responsible for inherited susceptibility to ovarian serous adenocarcinoma and mammary invasive ductal carcinoma. The finding of a germline mutation in PALB2 has implications for the patient and her family.....
.... Apart from BRCA1/2, the basis for genetic susceptibility to breast and ovarian cancer is heterogeneous, requiring sequential or multiplex testing. Panels directed towards breast and ovarian cancer susceptibility include genes like ATM, BRIP1, and PALB2.19 While this PALB2 deletion might have been detected using a panel approach, such methods are not designed to scan the entire genome. Although successful in diagnosing the underlying genetic susceptibility in up to 30% of BRCA1/2-negative familial breast cancer cases,19,20 panels are limited by the current state of knowledge of known or presumed cancer susceptibility genes, whereas the approach demonstrated here could potentially uncover changes in novel susceptibility genes....
 http://jco.ascopubs.org/content/34/8/e61/T1.large.jpg

Correspondence/References: Intraperitoneal Therapy for Ovarian Cancer



open access

Twenty-four years ago, David Alberts and I wrote a letter to the Journal of Clinical Oncology to speak in favor of studying intraperitoneal (IP) therapy.1 Now, the editorial by Bookman and Brady2 on the article by Tewari et al3 merits comments on this long-running debate......

REFERENCES

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  7. 7.
  8. 8.
  9. 9.

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New immunotherapy trial launched to test cancer vaccine (London and Guildford)



Medical News Today

 
A new vaccine aimed at enabling the immune system to fight against advanced cancer is being trialled in London and Guildford.
Scientists are testing the effectiveness and safety of the vaccine which works by resembling the natural immune responses generated by the body against bacterial and viral infections.
All patients with any solid tumour, irrespective of their type of cancer and tumour genetic profile, are believed to have the potential to benefit from this sort of treatment.