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PARP inhibitors: a tsunami of indications in different malignancies.

Gaëlle HaddadMarie Christelle SaadéRoland EidFady Gh HaddadHampig Raphael Kourie
Published in: Pharmacogenomics (2021)
The evolution of precision medicine in the field of oncology has led to a radical change in the course of malignancies. PARP inhibitors are drugs that block the activity of the PARP enzyme responsible for base excision repair and have shown significant positive response when used for tumors lacking homologous recombination, namely high efficacy among BRCA-mutated tumors. Since 2014, when olaparib received an accelerated US FDA approval in ovarian cancer, we witnessed many other FDA approvals for olaparib, rucaparib, niraparib and talazoparib. Additionally, many Phase I, II and III trials were published presenting revolutionizing results. Other ongoing trials combined PARP inhibitors with checkpoint inhibitors. We aimed in this review to state the FDA approvals for PARP inhibitors in breast, ovarian, fallopian tube and primary peritoneal cancers, report the major published trials in high impact medical journals, and mention the ongoing trials combining these drugs with checkpoint inhibitors.
Keyphrases
  • dna damage
  • dna repair
  • healthcare
  • cell cycle
  • randomized controlled trial
  • case report
  • young adults
  • drug induced