Literature DB >> 21276604

Improved survival in non-Ashkenazi Jewish ovarian cancer patients with BRCA1 and BRCA2 gene mutations.

Robin A Lacour1, Shannon N Westin, Larissa A Meyer, Shana N Wingo, John O Schorge, Rebecca Brooks, David Mutch, Ashley Molina, Rebecca Sutphen, Mack Barnes, Jeffrey Elder, Deanna Teoh, C Bethan Powell, Veena Choubey, Stephanie Blank, Heather R Macdonald, Mark F Brady, Diana L Urbauer, Diane Bodurka, David M Gershenson, Karen H Lu.   

Abstract

OBJECTIVES: Previous studies report a survival advantage in ovarian cancer patients with Ashkenazi Jewish (AJ) breast cancer gene (BRCA) founder mutations. The purpose of this study was to determine if this association exists in patients with non-Ashkenazi Jewish (non-AJ) BRCA mutations. We also sought to account for "survival bias" by minimizing lead time that may exist between diagnosis and genetic testing.
METHODS: Patients with stage III/IV ovarian cancer and a non-AJ BRCA mutation, seen between January 1996 and July 2007, were identified from eight institutions. Patients with sporadic ovarian cancer were compared to similar cases, matched by age, stage, year of diagnosis, and vital status at time interval to BRCA testing. Progression-free (PFS) and overall survival (OS) were calculated by the Kaplan-Meier method. Multivariate Cox proportional hazards models were calculated for variables of interest. Fisher's exact test and chi-square were also used for analysis.
RESULTS: Ninety-five advanced stage ovarian cancer patients with non-AJ BRCA mutations and 183 sporadic controls were analyzed. Compared to sporadic ovarian cancer patients, non-AJ BRCA patients had longer PFS (27.9 months vs. 17.9 months, HR 0.61 [95% CI 0.43-0.86]) and OS (101.7 months vs. 54.3 months, HR 0.43 [95% CI 0.27-0.68]). BRCA status was an independent predictor of PFS and OS.
CONCLUSIONS: This multicenter study demonstrates a significant survival advantage in advanced stage ovarian cancer patients with non-AJ BRCA mutations, confirming the previous studies in the Jewish population. This improved survival was evident when accounting for the "survival bias" that coincides with genetic testing.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21276604      PMCID: PMC3310886          DOI: 10.1016/j.ygyno.2010.12.354

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  20 in total

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6.  Survival analysis in familial ovarian cancer, a case control study.

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8.  Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.

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9.  Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.

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10.  Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

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  16 in total

1.  An emerging entity: pancreatic adenocarcinoma associated with a known BRCA mutation: clinical descriptors, treatment implications, and future directions.

Authors:  Maeve A Lowery; David P Kelsen; Zsofia K Stadler; Kenneth H Yu; Yelena Y Janjigian; Emmy Ludwig; David R D'Adamo; Erin Salo-Mullen; Mark E Robson; Peter J Allen; Robert C Kurtz; Eileen M O'Reilly
Journal:  Oncologist       Date:  2011-09-20

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Review 4.  Genetic risk and gynecologic cancers.

Authors:  Laura L Holman; Karen H Lu
Journal:  Hematol Oncol Clin North Am       Date:  2012-02       Impact factor: 3.722

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7.  BRCA1 expression is epigenetically repressed in sporadic ovarian cancer cells by overexpression of C-terminal binding protein 2.

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9.  Clinical Considerations of BRCA1- and BRCA2-Mutation Carriers: A Review.

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10.  Predictive modeling using a somatic mutational profile in ovarian high grade serous carcinoma.

Authors:  Insuk Sohn; Chang Ohk Sung
Journal:  PLoS One       Date:  2013-01-10       Impact factor: 3.240

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