PARP-Inhibitors in BRCA-Associated Pancreatic Cancer

  • Anshul Bhalla Tufts Medical Center and Tufts University School of Medicine. Boston, MA, USA
  • Muhammad Wasif Saif Tufts Medical Center and Tufts University School of Medicine. Boston, MA, USA
Keywords: Drug Therapy, gemcitabine, Genes, BRCA1, BRCA2, Mutation, PALB2 protein, human, Pancreatic Neoplasms, Poly(ADP-ribose) Polymerases

Abstract

Recent data suggests that treatingpatients with pancreatic cancer that express mutations in BRCA1, BRCA2, and PALB2 with chemotherapy which targets the DNA repair defect in these cells, such as platinum based therapies or PARPi [poly (ADP-ribose) polymerase inhibitor], may be more beneficial in these patients. Moreover, further data also indicates the promise of combining PARPi with conventional chemotherapy. Authors summarize the data related to PARPi in BRCA-associated pancreatic cancer that was presented at the annual meeting of ASCO 2014. Enrolment on a clinical trial for patients who fit these criteria should be encouraged.

Image: Schematic representation of PARP and BRCA mediated DNA repair.

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Schematic representation of PARP and BRCA mediated DNA repair
Published
2014-07-28
How to Cite
BhallaA., & SaifM. (2014). PARP-Inhibitors in BRCA-Associated Pancreatic Cancer. JOP. Journal of the Pancreas, 15(4), 340-343. https://doi.org/10.6092/1590-8577/2690
Section
Highlights from the “50th ASCO Annual Meeting 2014”. Chicago, IL, USA. May 30 - June 3, 2014