| Literature DB >> 26724258 |
Heather H Cheng1, Colin C Pritchard2, Thomas Boyd3, Peter S Nelson4, Bruce Montgomery5.
Abstract
Understanding the molecular underpinnings of sensitivity to specific therapies will advance the goal of precision medicine in prostate cancer (PCa). We identified three patients with metastatic castration-resistant PCa (mCRPC) who achieved an exceptional response to platinum chemotherapy (not first-line treatment for PCa), despite disease progression on prior standard therapies. Using targeted next-generation sequencing on the primary and metastatic tumors, we found that all three patients had biallelic inactivation of BRCA2, a tumor suppressor gene critical for homologous DNA repair. Notably, two had germline BRCA2 mutations, including a patient without compelling family history who was diagnosed at age 66 yr. The third patient had somatic BRCA2 homozygous copy loss. Biallelic BRCA2 inactivation in mCRPC warrants further exploration as a predictive biomarker for sensitivity to platinum chemotherapy.Entities:
Keywords: BRCA2; Carboplatin; DNA repair; Platinum; Prostate cancer; mCRPC
Mesh:
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Year: 2015 PMID: 26724258 PMCID: PMC4909531 DOI: 10.1016/j.eururo.2015.11.022
Source DB: PubMed Journal: Eur Urol ISSN: 0302-2838 Impact factor: 20.096