Evidence for the efficacy of iniparib, a PARP-1 inhibitor, in BRCA2-associated pancreatic cancer

David R. Fogelman, Robert A. Wolff, Scott Kopetz, Milind Javle, Charles Bradley, Isabel Mok, Fernando Cabanillas, James L. Abbruzzese

Research output: Contribution to journalArticlepeer-review

89 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)1417-1420
Number of pages4
JournalAnticancer research
Volume31
Issue number4
StatePublished - Apr 2011

Keywords

  • BRCA
  • Chemotherapy
  • Iniparib
  • Pancreatic cancer

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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