Comparison of poly (ADP-ribose) polymerase inhibitors (parpis) as maintenance therapy for platinum-sensitive ovarian cancer: Systematic review and network meta-analysis

Amos Stemmer, Inbal Shafran, Salomon M. Stemmer*, Daliah Tsoref

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background: Three PARPis (olaparib, niraparib and rucaparib) are currently FDA-approved as maintenance therapy in newly diagnosed and recurrent ovarian cancer. However, thus far, no trial has compared the three approved PARPis in the overall population, in patients with BRCA mutations, or in those with wild-type BRCA. Methods: A frequentist network meta-analysis was used for indirect comparisons between the different PARPis with respect to progression free survival (PFS), overall survival (OS), and adverse events. Results: Overall, six randomized clinical trials involving 2,770 patients, were included in the analysis. Results from the indirect comparisons revealed no statistically significant differences between the three PARPis with respect to PFS or OS in the entire population and in patients with mutated and wild-type BRCA, separately. Niraparib showed a statistically significant increased risk for grade 3 and 4 thrombocytopenia (risk-difference [RD] from placebo: 0.3; 95% confidence interval [CI], 0.27-0.34) and any grade neutropenia (RD from placebo: 0.22; 95% CI, 0.18-0.25) as compared with the other PARPis. Conclusion: No statistically significant difference was found between the three PARPis with respect to PFS or OS (overall and in subpopulations by BRCA status). There is, however, a statistical difference in toxicity as niraparib is associated with a greater risk for thrombocytopenia and neutropenia.

Original languageEnglish
Article number3026
Pages (from-to)1-12
Number of pages12
JournalCancers
Volume12
Issue number10
DOIs
StatePublished - Oct 2020

Keywords

  • Adverse event
  • Network meta-analysis
  • Ovarian cancer
  • Overall survival
  • Platinum-sensitive
  • Poly (ADP-ribose) polymerase inhibitor
  • Progression-free survival

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