A pan-tumor review of the role of poly(adenosine diphosphate ribose) polymerase inhibitors

CA Cancer J Clin. 2025 Jan 10. doi: 10.3322/caac.21870. Online ahead of print.

Abstract

Poly(adenosine diphosphate ribose) polymerase (PARP) inhibitors, such as olaparib, talazoparib, rucaparib, and niraparib, comprise a therapeutic class that targets PARP proteins involved in DNA repair. Cancer cells with homologous recombination repair defects, particularly BRCA alterations, display enhanced sensitivity to these agents because of synthetic lethality induced by PARP inhibitors. These agents have significantly improved survival outcomes across various malignancies, initially gaining regulatory approval in ovarian cancer and subsequently in breast, pancreatic, and prostate cancers in different indications. This review offers a comprehensive clinical overview of PARP inhibitor approvals, emphasizing their efficacy across different cancers based on landmark phase 3 clinical trials.

Keywords: breast cancer; ovarian cancer; pancreatic cancer; poly(adenosine diphosphate ribose) polymerase inhibitors; prostate cancer.

Publication types

  • Review