M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Anticancer Res. 2011 Apr;31(4):1417-20.
Pancreatic cancer is an aggressive, frequently fatal malignancy that strikes 37,000 patients annually in the U.S.A. It is poorly responsive to standard chemotherapies such as gemcitabine. Approximately 5-10% of pancreatic cancer occurs in the setting of a BRCA2 mutation. Breast and ovarian carcinomas that harbor BRCA2 mutations are susceptible to the effects of an emerging class of targeted agents, namely, poly(ADP-ribose) polymerase (PARP) inhibitors. This report describes the case of a patient with a germline BRCA2 mutation and an associated pancreatic cancer treated with iniparib (BSI-201), a PARP inhibitor, who demonstrated a complete pathologic response to this agent. This case highlights the potential benefit for PARP inhibition in BRCA2-related pancreatic cancer.
胰腺癌在美国每年侵袭 3.7 万名患者,是一种侵袭性的、常致命的恶性肿瘤,对吉西他滨等标准化疗药物反应不佳。约 5-10%的胰腺癌发生在 BRCA2 突变的背景下。携带 BRCA2 突变的乳腺癌和卵巢癌易受一类新兴靶向药物的影响,即多聚(ADP-核糖)聚合酶(PARP)抑制剂的影响。本报告描述了一例携带胚系 BRCA2 突变和相关胰腺癌的患者,该患者接受了 PARP 抑制剂尼拉帕尼(BSI-201)治疗,该患者对该药物表现出完全的病理缓解。本病例突出了 PARP 抑制在 BRCA2 相关胰腺癌中的潜在获益。