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Wednesday, October 05, 2016

The impact of paclitaxel and carboplatin chemotherapy on the autonomous nervous system of patients with ovarian cancer (+heart systems)




sen·so·ri·mo·tor
ˌsen(t)sərēˈmōdər/adjective
Physiology adjective: sensorimotor (of nerves or their actions) having or involving both sensory and motor functions or pathways.
                                  ~~~~~~~~~~~~~~~~~~~~~~
open access - | BMC Neurology | Full Text
October 1, 2016

Background

Paclitaxel-based regimens are frequently associated with the development of peripheral neuropathy. The autonomous nervous system (ANS) effects, however, of this chemotherapeutic agent remain unexplored.

Methods

We investigated a group of 31 female patients with ovarian cancer receiving treatment with paclitaxel and carboplatin, as well as a group of 16 healthy age- and gender-matched healthy volunteers. All study participants completed a questionnaire and were assessed neurophysiologically at three time points (baseline, 3–4 months and 6–8 months following the onset of chemotherapy). The evaluation of the ANS included assessment of the adrenergic cardiovascular function (orthostatic hypotension-OH), parasympathetic heart innervation (30/15 ratio) and sympathetic skin response (SSR).

Results

At the 3–4 months ANS assessment, 19.2 % of the patients had systolic OH and the same percentage had diastolic OH, but at the 6–8 months evaluation no patient had systolic OH and only 13.8 % had diastolic OH. The values of the 30/15 ratio were significantly reduced at both time points, whereas the SSR was not affected.

Conclusions

Combined paclitaxel and carboplatin chemotherapy is associated with significant effects on the parasympathetic heart innervation and occasionally with effects on the adrenergic cardiovascular reaction. The SSR remained unaffected. Physicians should be alert to the possibility of these treatment-emergent side effects, so as to monitor ANS parameters and introduce treatment modifications accordingly. Our findings however, should be validated in larger cohorts.

Background

Paclitaxel is commonly used as first-line chemotherapy for advanced ovarian cancer and as adjuvant treatment, in combination with cisplatin or carboplatin, for residual disease. Taxanes (paclitaxel and docetaxel) are associated with numerous side effects, particularly including neurotoxic phenomena [1] . For instance, severe peripheral neuropathy is known to occur in patients receiving cumulative doses of around 1000 mg/m2 paclitaxel and 400 mg/m2 docetaxel [2]. In recent years, research interest focused on maximizing the therapeutic efficacy of paclitaxel, while minimizing the associated side effects. Despite these efforts, primarily sensory and occasionally sensorimotor [3, 4] peripheral neuropathy occurs in 59 to 78 % of treated patients [5, 6, 7].
Generalized peripheral neuropathies are frequently accompanied by autonomous nervous system (ANS) dysfunction [8]. However, it is currently unknown whether paclitaxel or its combination with carboplatin affects the ANS and whether paclitaxel-induced neuropathy comprises autonomic phenomena, as well.
The present study was designed to address this issue and investigate the effects of the combination of paclitaxel and carboplatin chemotherapy on the ANS. From a clinical point of view, paclitaxel is occasionally associated with hypotension, bradycardia and hypertension. Accordingly, we investigated the impact of paclitaxel on the sympathetic and parasympathetic innervation of the heart....

 Conclusions
The present study highlights the fact that combined paclitaxel and carboplatin chemotherapy for ovarian cancer is associated with significant effects on the sympathetic and parasympathetic heart innervation, whereas the SSR remains relatively untouched. Physicians caring for patients with ovarian cancer should be alert to the possibility of these treatment-emergent side effects, so as to monitor ANS parameters (BP, cardiac rhythm and their alterations upon standing) and introduce treatment modifications accordingly. Our findings however, should be validated in larger cohorts.

Abbreviations

ANS: 
Autonomous nervous system
BP: 
Blood pressure
DBP: 
Diastolic blood pressure
NCVs: 
Nerve conduction velocities
OH: 
Orthostatic hypotension
OS: 
Overall survival
PFS: 
Progression-free survival
SBP: 
Systolic blood pressure
SD: 
Standard deviation
SSR: 
Sympathetic skin response

SGO collaboration (new) Genetics Toolkit (Lynch Syndrome/BRCA/variants....)



Genetics Toolkit | SGO

A collaboration of the Society of Gynecologic Oncology, the American College of Obstetricians and Gynecologists, the National Society of Genetic Counselors, Bright Pink and Facing Our Risk of Cancer Empowered (FORCE)
 

The Society of Gynecologic Oncology has partnered with medical societies and patient advocacy groups to develop a toolkit designed to provide critical, practical information to heath care provers interested in gaining a deeper understanding of the role of genetics in gynecologic cancers. While not written for a lay audience, patients and families will gain an appreciation for the complexity of genetic testing and the challenges providers face every day.

The toolkit is comprised of specific case studies telling an individual woman’s story. Key points are illuminated from each organization’s perspective. Each case history provides references, national guidelines and society statements. A “General Resources” section includes useful tools and websites of interest.

Society of Gynecologic Oncology Genetics Toolkit (Complete version)
Case 1: BRCA1- and BRCA2-related ovarian cancer
Case 2: Daughter of BRCA1 mutation carrier
Case 3: Risk-reducing salpingo-oophorectomy
Case 4: Health outcomes after risk-reducing salpingo-oophorectomy
Case 5: Impact of hereditary breast and ovarian cancer genes on male family members
Case 6: Ambiguous test results and variants
Case 7: Lynch syndrome
General Resources
Collaborating Organizations

ESMO 2016 conference (Oct 7-11) 3 presidential sessions (niraparib/ovarian)



Medscape 


Taking place from October 7 to 11 in Copenhagen, this is the largest oncology meeting in Europe, say the organizers, who are expecting more than 20,000 attendees listening to 1600 approved abstracts, of which 50 will be reporting late-breaking trials. This will form part of 21 tumor tracks covering all areas of oncology, from basic science to clinical activities and public health.
Andrés Cervantes, MD, professor of medicine at the University of Valencia, Spain, and Scientific Committee chair for ESMO 2016, explained that so many trials are being reported at the meeting that are predicted to have an impact on clinical practice that there will be not one but three presidential sessions.
The first presidential symposium takes place on Saturday, October 8, and will discuss three abstracts that feature new investigational agents. The first will discuss results from the MONALEESA-2 study, which looked at the investigational CDK4/6 inhibitor ribociclib (formerly LEE011, Novartis) used with letrozole (Femara, Novartis) in postmenopausal women with hormone receptor–positive, HER2-negative advanced breast cancer. In the same session, results will be presented from a randomized study on the use of a new PARP (poly [ADP-ribose] polymerase) inhibitor niraparib, which is under development by Tesaro, in patients with platinum-sensitive ovarian cancer.

Smart Patients and AliveAndKickn: Lynch Syndrome online community



Smart Patients
 
AliveAndKickn is a proud to partner with Smart Patients, an online community for patients and caregivers affected by Lynch Syndrome and associated cancers. The online support of the Smart Patients Lynch Syndrome Community complements the work of AliveAndKickn, whose mission is to improve the lives of individuals and families affected by Lynch Syndrome and associated cancers through research, education, and screening.
Join Smart Patients, ask a question, and support others who can learn from you.

(blog) Plaintiff Attys Seek 3rd Win Against J&J At Trial Over Talc Powder's Supposed Cancer Risk



legal blog

Canada Denies Public Access To Potentially Life-Prolonging (oral) Ovarian Cancer Treatment LYNPARZA® (olaparib)



News Press Release | PharmiWeb.com

AstraZeneca Canada
Canada NewsWire
MISSISSAUGA, ON, Oct. 5, 2016

Pan-Canadian Oncology Drug Review (pCODR) Decides not to Recommend Lynparza for Reimbursement
MISSISSAUGA, ON, Oct. 5, 2016 /CNW/ - Following its deliberations, the pan-Canadian Oncology Drug Review (pCODR) recently announced its decision not to recommend for provincial reimbursement, Lynparza (olaparib), a maintenance treatment for women with platinum-sensitive relapsed BRCA-mutated (germline or somatic) high grade serous epithelial ovarian, fallopian tube or primary peritoneal cancer. AstraZeneca Canada is extremely disappointed that pCODR has disregarded the demonstrated significant clinical benefits of Lynparza, including potentially prolonging life, creating a roadblock for Canadian women in accessing the first oral, targeted therapy for BRCA-mutated relapsed ovarian cancer
"We are surprised and deeply disappointed in pCODR's assessment of Lynparza," says Mark Findlay, Vice President, Patient Access & Established Brands, AstraZeneca Canada. "Regulatory bodies around the world, Canadian oncologists and patient organizations have all demonstrated strong support for this important advancement in ovarian cancer treatment. Additionally, women from many countries with similar reimbursement agencies as pCODR, such as the UK, France, Norway, Denmark and Sweden, already have access to this treatment option as a result of reimbursement of Lynparza; Canadian women deserve no less. We are committed to working with provincial governments to urgently address the issue of access to Lynparza for Canadian women with relapsed ovarian cancer."
In its assessment, pCODR questioned the clinical benefits of Lynparza, despite Health Canada, the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA) and many regulatory bodies around the world having assessed and approved Lynparza based on its efficacy and safety data. Lynparza was first approved by the FDA in 2014 following an accelerated approval. Since then, more than 45 countries have approved Lynparza, several of which have also provided accelerated approval.1 The pCODR recommendation not to list means that, for many Canadian women, it will be more difficult to receive coverage for a medicine that has been reimbursed and available to patients in many countries since 2014. Canadian women with ovarian cancer are at a distinct disadvantage, as Canada is now falling behind emerging economies, including Greece, Romania, Hungary and Poland, when it comes to providing public funding for this innovative, targeted therapy.2

Effect of ARID1A/BAF250a expression on carcinogenesis and clinicopathological factors in pure-type clear cell adenocarcinoma of the ovary (Japan)



Blogger's Note: important to note that clear cell ovarian cancer is diagnosed at significantly higher rates than other countries and may represent a distinct phenotype

open access:
Effect of ARID1A/BAF250a expression on carcinogenesis and clinicopathological factors in pure-type clear cell adenocarcinoma of the ovary

Frequent mutation of the ARID1A gene has been recently identified in ovarian clear‑cell adenocarcinoma (CCA); however, the clinical significance of BAF250a expression encoded by the ARID1A gene remains to be determined. The aim of the present study was to assess whether BAF250a expression had an impact on the clinical features of CCA....Although loss of BAF250a expression was associated with early tumorigenesis in endometriosis‑related CCA, this alteration was not significantly correlated with chemosensitivity and prognoses of CCA. Further biomarker analyses, including BAF250a expression, are required to improve the prognoses of CCA.
 Patients
A total of 97 cases of CCA treated between 1984 and 2007 at the National Defense Medical College Hospital, (Tokorozawa, Japan) were enrolled in the present study. Of the 97 CCAs, a consecutive series of 38 CCAs synchronous with endometriosis (EM-related CCAs) and 21 CCAs adjacent to CCAF component (CCAF-related CCAs) were identified, according to the histopathological criteria described previously (18). Of those, 31 non-atypical endometrioses, 38 atypical endometrioses, 20 benign CCAFs and 21 borderline CCAFs were identified. A total of 18 cases with solitary endometriosis that had no CCA were used as controls.
 

Reproductive and hormonal factors in relation to survival and platinum resistance among ovarian cancer cases



Abstract:
 Reproductive and hormonal factors in relation to survival and platinum resistance among ovarian cancer cases : British Journal of Cancer
 
Background:
Ovarian cancer survival is poor, particularly for platinum-resistant cases. The previous literature on pre-diagnostic reproductive factors and ovarian cancer survival has been mixed. Therefore, we evaluated pre-diagnostic reproductive and hormonal factors with overall survival and, additionally, platinum-chemotherapy resistance.
Methods:
We followed 1649 invasive epithelial ovarian cancer cases who were enrolled between 1992 and 2008 for overall mortality within the New England Case-Control Study and abstracted chemotherapy data on a subset (n=449). We assessed pre-diagnostic reproductive and hormonal factors during in-person interviews. We calculated hazard ratios (HRs) using Cox-proportional hazards models.
Results:
We observed 911 all-cause deaths among 1649 ovarian cancer cases. Self-reported endometriosis and longer duration of hormone therapy use were associated with improved survival (HR: 0.72; 95% confidence interval (CI): 0.54–0.94 and HR, greater than or equal to5 years vs never: 0.70; 95% CI: 0.55–0.90, respectively). Older age at menopause and menarche were associated with worse survival (HR, less than or equal to50 vs >50 years: 1.23; 95% CI: 1.03–1.46 and HR, 13 vs <13 years: 1.24; 95% CI: 1.06–1.44, respectively). We observed no association between oral contraceptive use, parity and tubal ligation, and overall survival. No significant associations were observed for any of the reproductive and hormonal factors and platinum resistance.
Conclusions:
These results suggest that pre-diagnostic exposures such as endometriosis and HT use may influence overall survival among ovarian cancer patients.

The generalizability of NCI-sponsored clinical trials accrual among women with gynecologic malignancies



abstract:
The generalizability of NCI-sponsored clinical trials accrual among women with gynecologic malignancies
 

Highlights

  • The population enrolled to gynecologic cancer clinical trials differs from the US population
  • Extremes of age, racial and ethnic minorities in are under-represented in these clinical trials
  • Several factors including geography influence the diversity of clinical trials accruals

Objectives

Enrollment of a representative population to cancer clinical trials ensures scientific reliability and generalizability of results. This study evaluated the similarity of patients enrolled in NCI-supported group gynecologic cancer trials to the incident US population.

Methods

Accrual to NCI-sponsored ovarian, uterine, and cervical cancer treatment trials between 2003 and 2012 were examined. Race, ethnicity, age, and insurance status were compared to the analogous US patient population estimated using adjusted SEER incidence data.

Results

There were 18,913 accruals to 156 NCI-sponsored gynecologic cancer treatment trials, ovarian (56%), uterine (32%), and cervical cancers (12%). Ovarian cancer trials included the least racial, ethnic and age diversity. Black women were notably underrepresented in ovarian trials (4% versus 11%). Hispanic patients were underrepresented in ovarian and uterine trials (4% and 5% versus 18% and 19%, respectively), but not in cervical cancer trials (14 versus 11%). Elderly patients were underrepresented in each disease area, with the greatest underrepresentation seen in ovarian cancer patients over the age of 75 (7% versus 29%). Privately insured women were overrepresented among accrued ovarian cancer patients (87% versus 76%), and the uninsured were overrepresented among women with uterine or cervical cancers. These patterns did not change over time.

Conclusions

Several notable differences were observed between the patients accrued to NCI funded trials and the incident population. Improving representation of racial and ethnic minorities and elderly patients on cancer clinical trials continues to be a challenge and priority.

(weight loss - gyn + breast pts) Aspects of Health-Related Factors and Nutritional Care Needs by Survival Stage among Female Cancer Patients (South Korea)



open access
Aspects of Health-Related Factors and Nutritional Care Needs by Survival Stage among Female Cancer Patients in South Korea
 

Introduction

Over 2.4 million South Korean women were diagnosed with a female cancer (site of breast, cervix uteri, corpus uteri, or ovary) in 2012....
.... In addition, there are some national health/medical care systems for cancer patients in Korea with national health insurance systems as “Caner Control Act”, “Policy on Home-Based Management for Cancer” and “Policy on Hospice and Palliative Care for Terminal Cancer Patients” [2729]. However cancer patients still cannot be given better service. Those medical care systems are graded payment, and insufficient to cover the all patients and survivors. Regarding diet and nutrition managements, several hospitals are carrying out nutritional care, counselling, and education program, but it is not responsibility. Even there are no statistical figures to investigate the supports’ implementation status.....

Abstract

Purpose

This study examined diet-related problems and needs associated with nutritional care according to survival stage in Korean female cancer survivors.

Methods

186 outpatients (breast or gynecologic cancer survivors) recruited. Subjects were classified as (1) extended stage (ES, 2–5 years from diagnosis) and (2) long-term stage (LS, ≥5 years from diagnosis). Eating habits, changes in health related factors, nutritional needs, and quality of life were investigated.

Results

43% of ES survivors had diet-related problems (p = .031); ES group reported dyspepsia (indigestion) and LS group reported anorexia/nausea as the major problem. Half of ES survivors had taste change, decreasing amount of intake, and reduced quality of life (p < .05). The LS group had a greater preference for sweet tastes than the ES group. According to their diagnosis, ES survivors with breast cancer gained weight (27.1%), whereas ES survivors with gynecologic cancer lost their body weight (34.5%) significantly. LS breast cancer patients showed great food preference for vegetables, whereas those with gynecologic cancer showed an increased preference for fish, meat and grain. Approximately 90% of survivors demanded nutritional care regarding restricted foods, preventing recurrence, particularly in ES survivors (p < .01). Moreover, main factors for nutritional care needs were body weight control for breast cancer and food environment for gynecologic cancer.

Conclusion

Survivors have different aspects of diet-related problems by survival stage as dyspepsia in ES and anorexia in LS. ES stage had changes in dietary patterns and their food consumption have decreased. Most of survivors have demanded nutritional care regardless of survival stage. These features of each stage should be considered to improve their health.

Integrative Development of a TLR8 Agonist for Ovarian Cancer Chemo-immunotherapy



 Motolimod (formerly VTX-2337)

abstract

Background: Immunotherapy is an emerging paradigm for the treatment of cancer, but the potential efficacy of many drugs cannot be sufficiently tested in the mouse. We sought to develop a rational combination of motolimod-a novel Toll-like receptor 8 (TLR8) agonist that stimulates robust innate immune responses in humans but diminished responses in mice-with pegylated liposomal doxorubicin (PLD), a chemotherapeutic that induces immunogenic cell death.
Methods: We followed an integrative pharmacologic approach including healthy human volunteers, non-human primates, NSG-HIS ("humanized immune system") mice reconstituted with human CD34+ cells, and cancer patients to test the effects of motolimod and to assess the combination of motolimod with PLD for the treatment of ovarian cancer.
Results: The pharmacodynamic effects of motolimod monotherapy in NSG-HIS mice closely mimicked those in non-human primates and healthy human subjects, while the effects of the motolimod/PLD combination in tumor-bearing NSG-HIS mice closely mimicked those in patients with ovarian cancer treated in a phase 1b trial (NCT01294293). The NSG-HIS mouse helped elucidate the mechanism of action of the combination, and revealed a positive interaction between the two drugs in vivo. The combination produced no dose-limiting toxicities in ovarian cancer patients. Two subjects (15%) had complete responses and 7 subjects (53%) had disease stabilization. A phase 2 study was consequently initiated.
Conclusions: These results are the first to demonstrate the value of pharmacologic approaches integrating the NSG-HIS mouse, non-human primates, and cancer patients for the development of novel immunomodulatory anticancer agents with human specificity.

Tuesday, October 04, 2016

(popular writing) I Have Cancer and Haven't Learned Anything New About Life | Mother Jones



Blogger's Note: not about ovarian cancer but words many can relate to
Mother Jones

(Nfld, Canada) Evaluation of a Population Based Approach to Familial Colorectal Cancer



abstract

 As Newfoundland has the highest rate of familial CRC in the world, we started a population-based clinic to provide colonoscopic and Lynch syndrome (LS) screening recommendations to families of CRC patients based on family risk. Of 1091 incident patients 52% provided a family history. Seventy-two percent of families were at low or intermediate-low risk of CRC and colonoscopic screening recommendations were provided by letter. Twenty eight per cent were at high and intermediate-high risk and were referred to the genetic counsellor, but only 30% (N = 48) were interviewed by study end. Colonoscopy was recommended more frequently than every 5 years in 35% of families. Lower family risk was associated with older age of proband but the frequency of screening colonoscopy recommendations varied across all age groups, driven by variability in family history. Twenty four percent had a high MMR Predict score for a Lynch Syndrome mutation, and 23% fulfilled the Provincial Program criteria for LS screening. A population-based approach in the provision of colonoscopic screening recommendations to families at risk of CRC was limited by the relatively low response rate. A family history first approach to the identification of LS families was inefficient.

webcast Oct 26th: (Canada) CPSI and CIHI collaborate on Hospital Harm



Hospital Harm Measure

Webcast

October 26, 2016
Measuring Patient Harm in Canadian Hospitals Virtual Announcement
Join the expert panel to hear an announcement​ on Measuring Patient Harm in Canadian Hospitals and available Hospital Harm Improvement Resources to make care safer. 
Join us at 1 pm ET. 
Hospital Harm Project (anticipated release date: Fall 2016)

Hospital Harm Measure  
  • A new measure intended to monitor variations in patient safety in inpatient acute care settings at the national level.  across facilities over time.
  • It is designed to help identify patient safety improvement initiatives in hospitals and could be the basis of a future comparable indicator. 
  • The measure captures hospitalizations with at least one occurrence of unintended harm that could have potentially been prevented by implementing known evidence-informed practices.

journal (pdf) Cancer patterns and trends in Central and South America



 Blogger's Note: limited references to ovarian cancer

open access

Global Cancer Observatory: Cancer in Central and South America Project



Global Cancer Observatory

Cancer in Central and South America Project

The Cancer in Central and South America Project is a collaboration between the Section of Cancer Surveillance of the International Agency for Research on Cancer (IARC), the Red de Institutos e Instituciones Nacionales de Cáncer (RINC) and cancer registries in the Central and South American region. The project commenced in 2013, with the primary objective of collating data collected by these cancer registries; presenting the data in a standardized, comparable format; and making them available to cancer research and control communities within the region and elsewhere.

Three online resources are available from the Cancer in Central and South America Project:

Cancer in Central and South America

This supplement issue of the journal Cancer Epidemiology comprises a series of 17 peer-reviewed, open access papers describing the background, methodology and results of the project. Included in the collection are a broad overview of cancer incidence and mortality patterns within the region and 14 cancer site-specific papers looking in detail at the geographical and temporal patterns for the major cancers.
Cancer Epidemiology [Volume 44 Supplement 1] (2016)
  1. Foreword Wild CP, Delgado L.
  2. Cancer in Central and South America: Introduction Forman D.,Sierra MS.
  3. Cancer in Central and South America: Methodology Sierra MS,Forman D.
  4. Cancer patterns and trends in Central and South America Sierra MS, Soerjomataram I, Antoni S, Laversanne M, Piñeros M, de Vries E, Forman D.
  5. Head and neck cancer burden and preventive measures in Central and South America Perdomo S, Roa GM, Brennan P, Forman D, Sierra MS.
  6. The burden of oesophageal cancer in Central and South America Barrios E, Sierra MS, Musetti C, Forman D.
  7. Stomach cancer burden in Central and South America Sierra MS, Cueva P, Bravo LE, Forman D.
  8. Burden of colorectal cancer in Central and South America Sierra MS, Forman D.
  9. Burden of gallbladder cancer in Central and South America Izarzugaza MI, Fernández L, Forman D, Sierra MS.
  10. Descriptive epidemiology of lung cancer and current status of tobacco control measures in Central and South America Piñeros M, Sierra MS, Forman D.
  11. The burden of cutaneous melanoma and status of preventive measures in Central and South America de Vries E, Sierra MS, Loria D, Forman D.
  12. Female breast cancer in Central and South America Di Sibio A, Abriata G, Forman D, Sierra MS.
  13. Cervical cancer in Central and South America: Burden of disease and status of disease control Murillo R, Herrero R, Sierra MS, Forman D.
  14. Prostate cancer burden in Central and South America Sierra MS, Soerjomataram I, Forman D.
  15. Descriptive epidemiology of brain and central nervous system cancers in Central and South America Piñeros M, Sierra MS, Izarzugaza I, Forman D.
  16. Thyroid cancer burden in Central and South America Sierra MS, Soerjomataram I, Forman D.
  17. Hodgkin lymphoma burden in Central and South America Kusminsky G, Abriata G, Forman D, Sierra MS.
  18. The burden of non-Hodgkin lymphoma in Central and South America Diumenjo MC, Abriata G, Forman D, Sierra MS.
A complete list of the Cancer in Central and South America Working Group participants, including all the contributing registries is available here and the project's Editorial Board members are listed here.
Working Group members represented their respective cancer registries at the time of the call for data in 2013. Current contact information for cancer registries in the region can be found at the International Association of Cancer Registries (IACR) website.

Cancer in Central and South America - a comprehensive analysis (17 articles)



Medical News 

A series of 17 scientific articles coordinated by the International Agency for Research on Cancer (IARC), based on the most extensive collation of data on cancer incidence and mortality in Central and South America to date, will be published next week as a supplement issue of Cancer Epidemiology. The series provides a comprehensive analysis of recent cancer patterns in the region and can also be accessed on the IARC Global Cancer Observatory website, along with additional resources and statistics.

journal search "talc" - (AACR) Cancer Epidemiology, Biomarkers & Prevention



Search Results | Cancer Epidemiology, Biomarkers & Prevention

34 Results
for term "talc"
by: most recent first
  • Research Articles
    Association between Body Powder Use and Ovarian Cancer: The African American Cancer Epidemiology Study (AACES)
    Joellen M. Schildkraut, Sarah E. Abbott, Anthony J. Alberg, Elisa V. Bandera, Jill S. Barnholtz-Sloan, Melissa L. Bondy, Michele L. Cote, Ellen Funkhouser, Lauren C. Peres, Edward S. Peters, Ann G. Schwartz, Paul Terry, Sydnee Crankshaw, Fabian Camacho, Frances Wang and Patricia G. Moorman

    ...commentary by Trabert, p. 1369 Introduction Genital powder use may be a modifiable risk factor for epithelial ovarian cancer (EOC), the most deadly of all gynecologic cancers (1). In 2010, the International Agency for Research on Cancer (IARC) classified perineal (genital) use of nonasbestos–containing, talc ~~~
  • Commentary
    Body Powder and Ovarian Cancer Risk—What Is the Role of Recall Bias?
    Britton Trabert

    ..., specifically perineal talc use, has been suggested as another potential proinflammatory exposure that may be related to ovarian cancer risk. Several case–control studies have shown an association between genital powder use and increased risk of ovarian cancer (6–9). The International Agency for Research ~~~
  • Research Article
    Is pelvic inflammatory disease a risk factor for ovarian cancer?
    Christina B. Rasmussen, Allan Jensen, Vanna Albieri, Klaus K Andersen and Susanne K. Kjaer

    ...risk factors for ovarian cancer, including endometriosis, talc use and pelvic inflammatory disease (PID), may act through a common inflammatory mechanism. In addition, studies have shown that tubal ligation and hysterectomy protects against ovarian cancer (3) and this protective effect may also ~~~
  • Research Articles
    Chronic Recreational Physical Inactivity and Epithelial Ovarian Cancer Risk: Evidence from the Ovarian Cancer Association Consortium
    Rikki Cannioto, Michael J. LaMonte, Harvey A. Risch, Chi-Chen Hong, Lara E. Sucheston-Campbell, Kevin H. Eng, J. Brian Szender, Jenny Chang-Claude, Barbara Schmalfeldt, Ruediger Klapdor, Emily Gower, Albina N. Minlikeeva, Gary R. Zirpoli, Elisa V. Bandera, Andrew Berchuck, Daniel Cramer, Jennifer A. Doherty, Robert P. Edwards, Brooke L. Fridley, Ellen L. Goode, Marc T. Goodman, Estrid Hogdall, Satoyo Hosono, Allan Jensen, Susan Jordan, on behalf of The Australian Ovarian Cancer Study Group, Susanne K. Kjaer, Keitaro Matsuo, Roberta B. Ness, Catherine M. Olsen, Sara H. Olson, Celeste Leigh Pearce, Malcolm C. Pike, Mary Anne Rossing, Elizabeth A. Szamreta, Pamela J. Thompson, Chiu-Chen Tseng, Robert A. Vierkant, Penelope M. Webb, Nicolas Wentzensen, Kristine G. Wicklund, Stacey J. Winham, Anna H. Wu, Francesmary Modugno, Joellen M. Schildkraut, Kathryn L. Terry, Linda E. Kelemen and Kirsten B. Moysich

    ..., former), education (less than high school, high school, some college, college graduate, graduate school), talc or genital powder use (no use, genital use, nongenital use), NSAIDs use ( once/week,......(click link above for all 34 articles per search "talc"

Body Powder and Ovarian Cancer Risk—What Is the Role of Recall Bias? (AACR)



(partial view) Cancer Epidemiology, Biomarkers

Serious drug side effects are massively underreported in medical papers



link to paper/media

An astonishing 64 per cent of drug or medical device side effects are left out of the published reports that clinicians so frequently base decisions on. This is the finding of a recent paper published in the journal PLOS Medicine by a team of UK researchers.

Opportunistic Salpingectomy: Benefits Do Not Outweigh Risks: The National Catholic Bioethics Quarterly



(partial view) The National Catholic Bioethics Quarterly (Philosophy Documentation Center)


 

10 Steps to ‘End Cancer As We Know It’ - Blue Ribbon Panel's 10 Recommendations (U.S.)



Oncology Times
 

Blue Ribbon Panel's 10 Recommendations

1. Engage patients to contribute their comprehensive tumor profile data to expand knowledge about what therapies work, in whom, and in which types of cancer. This recommendation would create a privacy-protected new national network in which patients could “pre-register” for clinical trials.
2. Establish a cancer immunotherapy clinical trials network devoted exclusively to discovering and evaluating immunotherapy approaches in oncology. This network could help to speed the development of new cancer vaccines.
3. Identify therapeutic targets to overcome drug resistance through studies that determine the mechanisms that lead cancer cells to become resistant to previously effective treatments.
4. Create a national ecosystem for sharing and analyzing cancer data so that researchers, clinicians, and patients will be able to contribute data, which will facilitate efficient data analysis. This ecosystem would link many of the largest U.S. data repositories.
5. Improve our understanding of fusion oncoproteins (so-called rogue proteins) in pediatric cancer and use new preclinical models to develop inhibitors that target them.
6. Accelerate the development of guidelines for routing monitoring and management of patient-reported symptoms to minimize debilitating side effects of cancer and its treatment.
7. Reduce cancer risk and cancer health disparities through approaches in development, testing and broad adoption of proven prevention strategies. These include tobacco control, colorectal cancer screening and HPV vaccination.
8. Predict response to standard treatments through retrospective analysis of patient specimens.
9. Create dynamic 3D maps of human tumor evolution to document the genetic lesions and cellular interactions of each tumor as it evolves from a precancerous lesion to advanced cancer. A 3-D cancer atlas would allow researchers to develop predictive models of tumor progression and response to treatment.
10. Develop new enabling cancer technologies to characterize tumors and test therapies. These include implantable microdosing drug devices and advanced imaging technologies to study cancers at extremely high resolution.

ESMO 2016 October 7-11 (link to abstract book)



ESMO 2016 | Oncology Conference
ESMO 2016

 Official Journal of the European Society for
Medical Oncology and the Japanese Society of Medical Oncology
Volume 27, 2016 Supplement 6
Abstract Book of the 41st ESMO Congress (ESMO 2016)
Copenhagen, Denmark, 7–11 October 2016


Monday, October 03, 2016

Effects of a (Alberta) Provincial-Wide Implementation of Screening for Distress on Healthcare Professionals' Confidence and Understanding of Person-Centered Care in Oncology



Blogger's Note: 1 gyn cancer patient included


open access
 Effects of a Provincial-Wide Implementation of Screening for Distress on Healthcare Professionals' Confidence and Understanding of Person-Centered Care in Oncology

Background: Although published studies report that screening for distress (SFD) improves the quality of care for patients with cancer, little is known about how SFD impacts healthcare professionals (HCPs).  
Objectives: This quality improvement project examined the impact of implementing the SFD intervention on HCPs' confidence in addressing patient distress and awareness of person-centered care. Patients and Methods: This project involved pre-evaluation and post-evaluation of the impact of implementing SFD. A total of 254 HCPs (cohort 1) were recruited from 17 facilities across the province to complete questionnaires. SFD was then implemented at all cancer care facilities over a 10-month implementation period, after which 157 HCPs (cohort 2) completed post-implementation questionnaires. At regional and community care centers, navigators supported the integration of SFD into routine practice; therefore, the impact of navigators was examined.  
Results: HCPs in cohort 2 reported significantly greater confidence in managing patients' distress and greater awareness about person-centered care relative to HCPs in cohort 1. HCPs at regional and community sites reported greater awareness in person-centeredness before and after the intervention, and reported fewer negative impacts of SFD relative to HCPs at tertiary sites. Caring for single or multiple tumor types was an effect modifier, with effects observed only in the HCPs treating multiple tumors.  
Conclusions: Implementation of SFD was beneficial for HCPs' confidence and awareness of person-centeredness. Factors comprising different models of care, such as having site-based navigators and caring for single or multiple tumors, influenced outcomes.

Crossing the Line (direct to consumer advertising)



JNCCN

NCCN Imaging Appropriate Use Criteria (20 types of cancer + ovarian cancer)



NCCN Imaging Appropriate Use Criteria

NCCN Imaging Appropriate Use Criteria (NCCN Imaging AUC™)

 NCCN Imaging AUC currently are available for 20 cancer types; the new NCCN Imaging AUC are available for:

  • Esophageal and Esophagogastric Junction Cancers
  • Gastric Cancer
  • Malignant Pleural Mesothelioma
  • Melanoma
  • Ovarian Cancer
  • Penile Cancer
  • Small Cell Lung Cancer
  • Thymomas and Thymic Carcinomas
About NCCN Imaging AUC™
NCCN Imaging Appropriate Use Criteria (NCCN Imaging AUC™) include information designed to support clinical decision-making around the use of imaging in patients with cancer and are based directly on the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®). NCCN Imaging AUC™ are available free of charge to registered users of NCCN.org
NCCN Imaging AUC™ include recommendations pertaining to cancer screening, diagnosis, staging, treatment response assessment, follow-up, and surveillance. Additional information includes the indication, imaging modality, and frequency of use, as well as clinical notes related to the specific recommendation. NCCN Imaging AUC™ also document information on disease stage and histology. All imaging procedures recommended in the NCCN Guidelines®, including radiographs, computed tomography (CT) scans, magnetic resonance imaging (MRI), functional nuclear medicine imaging (PET, SPECT) and ultrasound, are included within NCCN Imaging AUC™.
NCCN Imaging AUC™ are accessible through an easy to use web-based user interface. The NCCN Imaging AUC™ include a full complement of imaging AUC in oncology care. NCCN, a CMS-approved Provider Led Entity (PLE), is committed to assuring that the most up-to-date recommendations are available and reviews and updates NCCN Imaging AUC™ on a continual basis to ensure that the recommendations take into account the most current evidence.

Apply for a Research Grant | The Rivkin Center for Ovarian Cancer research



Apply for a Research Grant

 The Rivkin Center has multiple streams of funding to support ovarian cancer research. Please see the following links for current requests for applications, guidelines, and forms.

2016 ESC Position Paper on cancer treatments and cardiovascular toxicity



open access:
2016 ESC Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines | European Heart Journal

 Embedded Image
 aWhen used in combination with anthracyclines and cyclophosphambIn patients receiving concurrent anthracyclines

 
1. Introduction
Advances in treatment have led to improved survival of patients with cancer, but have also increased morbidity and mortality due to treatment side effects.1,2 Cardiovascular diseases (CVDs) are one of the most frequent of these side effects, and there is a growing concern that they may lead to premature morbidity and death among cancer survivors.3 This may be the result of cardiotoxicity, which involves direct effects of the cancer treatment on heart function and structure, or may be due to accelerated development of CVD, especially in the presence of traditional cardiovascular risk factors.4
Although the field of cardio-oncology has received increasing attention in recent years, many aspects of both radiation-induced and cancer drug–induced CVD are still to be fully elucidated. Furthermore, the inability to predict the long-term consequences of cancer treatment–associated cardiovascular side effects leads to under- or overdiagnosis of CVD, sometimes resulting in the failure to prevent adverse events and sometimes to inappropriate interruption of a potentially lifesaving cancer treatment.
The complex issue of CVD as a consequence of previous cancer treatment requires the creation of multidisciplinary teams involving specialists in cardiology, oncology and other related fields.....

Abbreviations and acronyms

2-D
two-dimensional
3-D
three-dimensional
5-FU
5-fluorouracil
ACE
angiotensin-converting enzyme
ARB
angiotensin II receptor blocker
ASE
American Society of Echocardiography
BNP
B-type natriuretic peptide
CABG
coronary artery bypass graft
CAD
coronary artery disease
CHA2DS2-VASc
Congestive heart failure or left ventricular dysfunction, Hypertension, Age ≥75 (doubled), Diabetes, Stroke (doubled)-Vascular disease, Age 65–74, Sex category (female)
CMR
cardiac magnetic resonance
COT
registry Cardiac Oncology Toxicity registry
CT
computed tomography
CTRCD
Cancer Therapeutics–Related Cardiac Dysfunction
CVD
cardiovascular disease
EACVI
European Association of Cardiovascular Imaging
ECG
electrocardiogram / electrocardiographic
ESC
European Society of Cardiology
GLS
global longitudinal strain
GY
gray
HAS-BLED
Hypertension, Abnormal renal/liver function (1 point each), Stroke, Bleeding history or predisposition, Labile international normalized ratio, Elderly (>65 years), Drugs/alcohol concomitantly (1 point each)
HDAC
histone deacetylase
HER2
human epidermal growth factor receptor 2
HF
heart failure
LMWH
low molecular weight heparin
LV
left ventricle / left ventricular
LVEF
left ventricular ejection fraction
NA
not available
NOAC
non-vitamin K antagonist oral anticoagulant
NT-proBNP
N-terminal pro-B-type natriuretic peptide
NYHA
New York Heart Association
PAD
peripheral artery disease
PAH
pulmonary arterial hypertension
PCI
percutaneous coronary intervention
RCT
randomized controlled trial
T-DM1
trastuzumab-emtansine
TKI
tyrosine kinase inhibitor
VEGF
vascular endothelial growth factor
VHD
valvular heart disease
VKA
vitamin K antagonist
VTE
venous thromboembolism
WHO
World Health Organization

Glaxo to pay $20 million for bribing doctors in China



pharma news

I Had to Get Cancer to Become a More Empathetic DoctorI Had to Get Cancer to Become a More Empathetic Doctor



abstract: Annals of Internal Medicine

 I am 80 and a retired infectious diseases physician. I have always thought of myself as caring, compassionate, and warm. I thought I knew what patients were feeling, but only now that I have a life-threatening illness do I understand what it's really like to be a patient.

HRT Benefits Premenopausal Women After Ovary Removal - Clinical Oncology News



Clinical Oncology News

 A U.K. study that evaluated the cost-effectiveness of risk-reducing salpingo-oophorectomy (RRSO), the most successful intervention to prevent ovarian cancer, has emphasized the importance of hormone replacement therapy (HRT) in premenopausal women after surgery.
 Original article (abstract): Specifying the ovarian cancer risk threshold of ‘premenopausal risk-reducing salpingo-oophorectomy’ for ovarian cancer prevention: a cost-effectiveness analysis J Med Genet 2016;53:9 591-599

Outcomes included in the analyses were OC, breast cancer (BC) and additional deaths from coronary heart disease. Total costs and effects were estimated in terms of quality-adjusted life-years (QALYs); incidence of OC and BC; as well as incremental cost-effectiveness ratio (ICER).

How Does Surgical Volume Affect Gynecologic Surgery Outcomes?



medscape

 .....We have been aware for some time that patients of higher-volume surgeons have lower perioperative morbidity. However, for gynecologic procedures, it has not been clear whether such an inverse relationship between surgical volume and outcomes is present.
Investigators performed a review and meta-analysis of 14 reports that included almost 750,000 gynecologic surgeries.[1] Eleven of these reports were based in the United States and the remainder were from Holland and Canada. Those who performed surgery once a month or less frequently were considered low-volume surgeons. Hysterectomy and myomectomy procedures were categorized as gynecologic surgeries, endometrial and ovarian cancer procedures as oncology surgeries, and midurethral sling and pelvic reconstructive procedures as urogynecologic surgeries.
Overall, high-volume surgeons tended to operate on patients with more comorbidities. For gynecologic surgeries, low-volume surgeons had higher rates of intraoperative complications such as ureteral, bladder, bowel, and vascular injuries, as well as postoperative morbidity such as wound complications, hemorrhage, ileus, bowel obstruction, and venous thromboembolism. For oncology surgeries, patients of low-volume surgeons had higher perioperative mortality. One report found that among women undergoing surgery for ovarian cancer, 5-year survival was significantly higher with high-volume surgeons. In the urogynecologic category, one study found a higher rate of overall complications among patients of low-volume surgeons. Another noted a higher rate of reoperation for mesh complications following sling procedures performed by low-volume surgeons.
Recently, leaders at three US academic health systems announced a "Take the Volume Pledge" campaign to prevent certain surgeries (none of which are gynecologic) from being performed by low-volume surgeons.[2] This important article suggests that hospitals and particularly payers will increasingly be scrutinizing gynecologic surgeons' volume. Accordingly, gynecologic surgeons would be prudent to assess their own experience level as they plan surgical management of their patients.
Thank you for taking the time to view this video. I'm Andrew Kaunitz.

 References
  1. Mowat A, Maher C, Ballard E. Surgical outcomes for low-volume vs high-volume surgeons in gynecology surgery: a systematic review and meta-analysis. Am J Obstet Gynecol. 2016;215:21-33. Abstract
  2. Urbach DR. Pledging to eliminate low-volume surgery. N Engl J Med. 2015;373:1388-1390. Abstract

Cancer mortality differs among Asian ethnic groups



Medical News Today

Cancer not mainly down to 'bad luck,' finds stem cell study (but....)



Medical News 

In January 2015, a study published in the journal Science suggested that 22 of 31 cancer types - including ovarian, pancreatic, and bone cancers - were down to random "accidental" mutations that arise in normal adult stem cells as they divide.
The new research, however - led by Dr. Ruben van Boxtel of the Department of Genetics at University Medical Center Utrecht in the Netherlands - suggests these "bad luck" mutations do not contribute to cancer development as much as last year's report claims.

Sunday, October 02, 2016

Cancer immunotherapy is moving fast. Here’s what you need to know (media)



The Washington Post

 ......Over the next decade, the growth in the field will be "exponential," predicts Philip Greenberg, head of the immunology program at the Fred Hutchinson Cancer Research Center. "Making something better is enormously different than making something work that doesn't work."
At the same time, researchers remember the past anti-cancer efforts that fizzled after initially showing promise. That explains the consensus sentiment at this week's international immunotherapy conference in New York: Turning science into cures will take years of perseverance against daunting hurdles.
Here's a primer about new treatments and how they work:
What is cancer immunotherapy?.....

Immunotherapy for Ovarian Cancer - Cancer Research Institute



Immunotherapy for Ovarian Cancer 


Cancer Research Institute LogoAbout

IMMUNOTHERAPY FOR OVARIAN CANCER

Current immunotherapies for ovarian cancer fall into six broad categories: monoclonal antibodies; checkpoint inhibitors and immune modulators; therapeutic vaccines; adoptive T cell transfer; oncolytic viruses; and adjuvant immunotherapies. Most of these therapies are still in early-phase testing (phase I and II) for ovarian cancer, but their successful use in other types of cancers suggests that they may ultimately prove useful for ovarian cancer as well.

Long and irregular menstrual cycles, polycystic ovary syndrome, and ovarian cancer risk...



abstract:
Long and irregular menstrual cycles, polycystic ovary syndrome, and ovarian cancer risk in a population-based case-control study

 Long and irregular menstrual cycles, a hallmark of polycystic ovary syndrome (PCOS), have been associated with higher androgen and lower sex hormone binding globulin levels and this altered hormonal environment may increase the risk of specific histologic subtypes of ovarian cancer. We investigated whether menstrual cycle characteristics and self-reported PCOS were associated with ovarian cancer risk among 2041 women with epithelial ovarian cancer and 2100 controls in the New England Case-Control Study (1992-2008). Menstrual cycle irregularity, menstrual cycle length, and PCOS were collected through in-person interview. Unconditional logistic regression models were used to calculate odds ratios (OR) and 95% confidence intervals (95% CIs) for ovarian cancer risk overall, and polytomous logistic regression to evaluate whether risk differed between histologic subtypes. Overall, we observed no elevation in ovarian cancer risk for women who reported periods that were never regular or for those reporting a menstrual cycle length of >35 days with ORs of 0.87 (95% CI=0.69-1.10) and 0.83 (95% CI=0.44-1.54), respectively. We observed no overall association between self-reported PCOS and ovarian cancer (OR=0.97; 95% CI=0.61-1.56). However, we observed significant differences in the association with menstrual cycle irregularity and risk of ovarian cancer subtypes (pheterogeneity=0.03) as well as by BMI and OC use (pinteraction<0.01). Most notable, menstrual cycle irregularity was associated with a decreased risk of high grade serous tumors but an increased risk of serous borderline tumors among women who had never used OCs and those who were overweight. Future research in a large collaborative consortium may help clarify these associations.

HHS Whiteboard on Health Care Data - YouTube (3:13 min) eg. patient access EHR



YouTube

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Published on Sep 27, 2016
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