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PMID: 20547991 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Validation Study

Gene expression profile of BRCAness that correlates with responsiveness to chemotherapy and with outcome in patients with epithelial ovarian cancer.

Konstantinopoulos PA, Spentzos D, Karlan BY, Taniguchi T, Fountzilas E, Francoeur N, Levine DA, Cannistra SA

Abstract

To define a gene expression profile of BRCAness that correlates with chemotherapy response and outcome in epithelial ovarian cancer (EOC). A publicly available microarray data set including 61 patients with EOC with either sporadic disease or BRCA(1/2) germline mutations was used for development of the BRCAness profile. Correlation with platinum responsiveness was assessed in platinum-sensitive and platinum-resistant tumor biopsy specimens from six patients with BRCA germline mutations. Association with poly-ADP ribose polymerase (PARP) inhibitor responsiveness and with radiation-induced RAD51 foci formation (a surrogate of homologous recombination) was assessed in Capan-1 cell line clones. The BRCAness profile was validated in 70 patients enriched for sporadic disease to assess its association with outcome. The BRCAness profile accurately predicted platinum responsiveness in eight out of 10 patient-derived tumor specimens, and between PARP-inhibitor sensitivity and resistance in four out of four Capan-1 clones. [corrected] When applied to the 70 patients with sporadic disease, patients with the BRCA-like (BL) profile had improved disease-free survival (34 months v 15 months; log-rank P = .013) and overall survival (72 months v 41 months; log-rank P = .006) compared with patients with a non-BRCA-like (NBL) profile, respectively. The BRCAness profile maintained independent prognostic value in multivariate analysis, which controlled for other known clinical prognostic factors. The BRCAness profile correlates with responsiveness to platinum and PARP inhibitors and identifies a subset of sporadic patients with improved outcome. Additional evaluation of this profile as a predictive tool in patients with sporadic EOC is warranted.

MeSH Terms
Adult Aged Aged, 80 and over Antineoplastic Agents/therapeutic use Cell Line, Tumor Disease-Free Survival Drug Resistance, Neoplasm Exonucleases/metabolism Female Gene Expression Profiling Genes, BRCA1 Genes, BRCA2 Humans Middle Aged Mutation Neoplasms, Glandular and Epithelial/drug therapy,genetics Ovarian Neoplasms/drug therapy,genetics Platinum Compounds/therapeutic use Poly(ADP-ribose) Polymerase Inhibitors Treatment Outcome
Chemicals
Antineoplastic Agents Platinum Compounds Poly(ADP-ribose) Polymerase Inhibitors Exonucleases Rad1 protein, human
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Konstantinopoulos Panagiotis A
Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Spentzos Dimitrios
Karlan Beth Y
Taniguchi Toshiyasu
Fountzilas Elena
Francoeur Nancy
Levine Douglas A
Cannistra Stephen A
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Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2010-08-01
Epub
2010-00-14
Pages
3555-61
Language
English
Region
United States
NLM ID
8309333
PMCID
PMC2917311
Subset
IM
Grants
NCI NIH HHS · P50 CA105009 · United States
Corrections
ErratumIn
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CommentIn
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