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PMID: 23257362 Published · ppublish English Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Prognostically relevant gene signatures of high-grade serous ovarian carcinoma.

The Journal of clinical investigation ·Vol. 123 ·No. 1 ·2013-01-00 ·Pages 517-25

Verhaak RG, Tamayo P, Yang JY, Hubbard D, Zhang H, Creighton CJ, Fereday S, Lawrence M, Carter SL, Mermel CH, Kostic AD, Etemadmoghadam D, Saksena G, Cibulskis K, Duraisamy S, Levanon K, Sougnez C, Tsherniak A, Gomez S, Onofrio R, Gabriel S, Chin L, Zhang N, Spellman PT, Zhang Y, Akbani R, Hoadley KA, Kahn A, Köbel M, Huntsman D, Soslow RA, Defazio A, Birrer MJ, Gray JW, Weinstein JN, Bowtell DD, Drapkin R, Mesirov JP, Getz G, Levine DA, Meyerson M, Cancer Genome Atlas Research Network

Abstract

Because of the high risk of recurrence in high-grade serous ovarian carcinoma (HGS-OvCa), the development of outcome predictors could be valuable for patient stratification. Using the catalog of The Cancer Genome Atlas (TCGA), we developed subtype and survival gene expression signatures, which, when combined, provide a prognostic model of HGS-OvCa classification, named "Classification of Ovarian Cancer" (CLOVAR). We validated CLOVAR on an independent dataset consisting of 879 HGS-OvCa expression profiles. The worst outcome group, accounting for 23% of all cases, was associated with a median survival of 23 months and a platinum resistance rate of 63%, versus a median survival of 46 months and platinum resistance rate of 23% in other cases. Associating the outcome prediction model with BRCA1/BRCA2 mutation status, residual disease after surgery, and disease stage further optimized outcome classification. Ovarian cancer is a disease in urgent need of more effective therapies. The spectrum of outcomes observed here and their association with CLOVAR signatures suggests variations in underlying tumor biology. Prospective validation of the CLOVAR model in the context of additional prognostic variables may provide a rationale for optimal combination of patient and treatment regimens.

MeSH Terms
Adult Aged BRCA1 Protein/biosynthesis,genetics BRCA2 Protein/biosynthesis,genetics Disease-Free Survival Female Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Middle Aged Models, Biological Mutation Neoplasm Grading Ovarian Neoplasms/classification,genetics,metabolism,mortality,therapy Predictive Value of Tests Prospective Studies Survival Rate
Chemicals
BRCA1 Protein BRCA1 protein, human BRCA2 Protein BRCA2 protein, human
Authors & Affiliations
42 authors, click to expand affiliations / ORCID
Verhaak Roel G W
Department of Bioinformatics and Computational Biology, MD Anderson Cancer Center, Houston, Texas 77030, USA. [email protected]
Tamayo Pablo
Yang Ji-Yeon
Hubbard Diana
Zhang Hailei
Creighton Chad J
Fereday Sian
Lawrence Michael
Carter Scott L
Mermel Craig H
Kostic Aleksandar D
Etemadmoghadam Dariush
Saksena Gordon
Cibulskis Kristian
Duraisamy Sekhar
Levanon Keren
Sougnez Carrie
Tsherniak Aviad
Gomez Sebastian
Onofrio Robert
Gabriel Stacey
Chin Lynda
Zhang Nianxiang
Spellman Paul T
Zhang Yiqun
Akbani Rehan
Hoadley Katherine A
Kahn Ari
Köbel Martin
Huntsman David
Soslow Robert A
Defazio Anna
Birrer Michael J
Gray Joe W
Weinstein John N
Bowtell David D
Drapkin Ronny
Mesirov Jill P
Getz Gad
Levine Douglas A
Meyerson Matthew
Cancer Genome Atlas Research Network
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
1558-8238
Published
2013-01-00
Epub
2012-00-21
Pages
517-25
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC3533304
Subset
IM
Grants
NIGMS NIH HHS · R01 GM074024 · United States
NCI NIH HHS · P30 CA016672 · United States
NCI NIH HHS · U24 CA143799 · United States
NIGMS NIH HHS · T32 GM007753 · United States
NCI NIH HHS · U24CA143867 · United States
NCI NIH HHS · U24 CA143883 · United States
NCI NIH HHS · R01 CA121941 · United States
NCI NIH HHS · U24 CA143867 · United States
NHGRI NIH HHS · U54 HG003067 · United States
NCI NIH HHS · P30 CA016056 · United States
NCI NIH HHS · P30 CA008748 · United States
NCI NIH HHS · U24CA143883 · United States
Corrections
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