Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer

  • Isabelle Ray-Coquard
  • Patricia Pautier
  • Sandro Pignata
  • David Pérol
  • Antonio González-Martín
  • Regina Berger
  • Keiichi Fujiwara
  • Ignace Vergote
  • Nicoletta Colombo
  • Johanna Mäenpää
  • Frédéric Selle
  • Jalid Sehouli
  • Domenica Lorusso
  • Eva M Guerra Alía
  • Alexander Reinthaller
  • Shoji Nagao
  • Claudia Lefeuvre-Plesse
  • Ulrich Canzler
  • Giovanni Scambia
  • Alain Lortholary
  • Frederik Marmé
  • Pierre Combe
  • Nikolaus de Gregorio
  • Manuel Rodrigues
  • Paul Buderath
  • Coraline Dubot
  • Alexander Burges
  • Benoît You
  • Eric Pujade-Lauraine
  • Philipp Harter
  • PAOLA-1 Investigators

Abstract

BACKGROUND: Olaparib has shown significant clinical benefit as maintenance therapy in women with newly diagnosed advanced ovarian cancer with a BRCA mutation. The effect of combining maintenance olaparib and bevacizumab in patients regardless of BRCA mutation status is unknown.

METHODS: We conducted a randomized, double-blind, international phase 3 trial. Eligible patients had newly diagnosed, advanced, high-grade ovarian cancer and were having a response after first-line platinum-taxane chemotherapy plus bevacizumab. Patients were eligible regardless of surgical outcome or BRCA mutation status. Patients were randomly assigned in a 2:1 ratio to receive olaparib tablets (300 mg twice daily) or placebo for up to 24 months; all the patients received bevacizumab at a dose of 15 mg per kilogram of body weight every 3 weeks for up to 15 months in total. The primary end point was the time from randomization until investigator-assessed disease progression or death.

RESULTS: Of the 806 patients who underwent randomization, 537 were assigned to receive olaparib and 269 to receive placebo. After a median follow-up of 22.9 months, the median progression-free survival was 22.1 months with olaparib plus bevacizumab and 16.6 months with placebo plus bevacizumab (hazard ratio for disease progression or death, 0.59; 95% confidence interval [CI], 0.49 to 0.72; P<0.001). The hazard ratio (olaparib group vs. placebo group) for disease progression or death was 0.33 (95% CI, 0.25 to 0.45) in patients with tumors positive for homologous-recombination deficiency (HRD), including tumors that had BRCA mutations (median progression-free survival, 37.2 vs. 17.7 months), and 0.43 (95% CI, 0.28 to 0.66) in patients with HRD-positive tumors that did not have BRCA mutations (median progression-free survival, 28.1 vs. 16.6 months). Adverse events were consistent with the established safety profiles of olaparib and bevacizumab.

CONCLUSIONS: In patients with advanced ovarian cancer receiving first-line standard therapy including bevacizumab, the addition of maintenance olaparib provided a significant progression-free survival benefit, which was substantial in patients with HRD-positive tumors, including those without a BRCA mutation. (Funded by ARCAGY Research and others; PAOLA-1 ClinicalTrials.gov number, NCT02477644.).

Bibliografische Daten

OriginalspracheEnglisch
ISSN0028-4793
DOIs
StatusVeröffentlicht - 19.12.2019
Extern publiziertJa

Anmerkungen des Dekanats

Copyright © 2019 Massachusetts Medical Society.

PubMed 31851799