PubMed · 2011 · 93 citations · 9 references
MedicineOncologyPharmacologyCancer PharmacologyChemotherapyMolecular OncologyCancer Molecular PathologyGermline Cancer SusceptibilityMalignant NeoplasmsPancreatic CancerPancreatic PathologyTargeted Cancer TherapyBrca MutationsBrca2 InactivationParp InhibitionParp Inhibitor ResistanceParp Inhibitor SensitivityPoly Adp-ribose Polymerase InhibitorsPoly(adp-ribose) Polymerase InhibitionPoly(adp-ribose) Polymerase Inhibitors
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.
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Inhibition of Poly(ADP-Ribose) Polymerase in Tumors from <i>BRCA</i> Mutation Carriers
Peter C.C. Fong, David S. Boss, Timothy A. Yap et al. · New England Journal of Medicine · 2009 · 3.6K citations · Full text
Medicine, Oncology, Pharmacology +17
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas.
Michael Goggins, Mieke Schutte, Jing Lü et al. · PubMed · 1996 · 648 citations
Involvement of Brca2 in DNA Repair
Ketan J. Patel, Veronica Yu, Hyun‐Sook Lee et al. · Molecular Cell · 1998 · 631 citations · Full text