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An In-Depth Review of Niraparib in Ovarian Cancer: Mechanism of Action, Clinical Efficacy and Future Directions.

Published version
Peer-reviewed

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Authors

Akay, Melek 
Funingana, Ionut-Gabriel 
Patel, Grisma 
Mustapha, Rami 
Gjafa, Ernese 

Abstract

Niraparib is an oral, potent, highly selective poly-ADP ribose polymerase 1 (PARP1) and PARP2 inhibitor. In most developed countries, it is approved as a maintenance treatment for epithelial ovarian, fallopian tube, or primary peritoneal cancer in patients with complete or partial response to platinum-based therapy. These approvals are based on results of randomised, double-blind, placebo-controlled trials, particularly the NOVA trial and more recently the PRIMA trial. In this comprehensive review, we delve into the scientific basis of PARP inhibition, discussing both preclinical and clinical data which have led to the current approval status of niraparib. We also discuss ongoing trials and biological rationale of combination treatments involving niraparib, with particular focus on antiangiogenic drugs, immune checkpoint inhibitors and cyclic GMP-AMP synthase stimulator of interferon genes (cGAS/STING) pathway. In addition, we reflect on potential strategies and challenges of utilising current biomarkers for treatment selection of patients to ensure maximal benefit.

Description

Keywords

Combined therapy, Niraparib, Ovarian Cancer, PARP inhibitors, Pharmacokinetics

Journal Title

Oncol Ther

Conference Name

Journal ISSN

2366-1070
2366-1089

Volume Title

9

Publisher

Springer Science and Business Media LLC