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A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment

  • Published:2017-08 Issue:2 Volume:146 Page:399-404
  • ISSN:0090-8258
  • Container-title:Gynecologic Oncology
  • language:en
  • Short-container-title:Gynecologic Oncology

Author:

Bednar Erica M.,Oakley Holly D.,Sun Charlotte C.,Burke Catherine C.,Munsell Mark F.,Westin Shannon N.,Lu Karen H.

Funder

The University of Texas MD Anderson Cancer Center

The MD Anderson Cancer Center Moon Shot™

NIH/NCI

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Oncology

Reference22 articles.

1. BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases;Pal;Cancer,2005

2. Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada;Risch;J. Natl. Cancer Inst.,2006

3. BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group;Alsop;J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol.,2012

4. Meta-analysis of BRCA1 and BRCA2 penetrance;Chen;J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol.,2007

5. Clinical Practice Guidelines in Oncology: Genetic/Familial High-Risk Assessment: Breast and Ovarian [Internet];NCCN,2008
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