Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer
- PMID: 31851799
- DOI: 10.1056/NEJMoa1911361
Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer
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.).
Copyright © 2019 Massachusetts Medical Society.
Comment in
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Personalized Medicine for Primary Treatment of Serous Ovarian Cancer.N Engl J Med. 2019 Dec 19;381(25):2471-2474. doi: 10.1056/NEJMe1914488. N Engl J Med. 2019. PMID: 31851805 No abstract available.
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Olaparib plus bevacizumab improves progression-free survival in ovarian cancer.Lancet Oncol. 2020 Feb;21(2):e71. doi: 10.1016/S1470-2045(20)30005-X. Epub 2020 Jan 9. Lancet Oncol. 2020. PMID: 31928926 No abstract available.
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PARP Inhibitors in Ovarian Cancer.N Engl J Med. 2020 Apr 16;382(16):1573. doi: 10.1056/NEJMc2000644. N Engl J Med. 2020. PMID: 32294362 No abstract available.
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PARP Inhibitors in Ovarian Cancer.N Engl J Med. 2020 Apr 16;382(16):1573-1574. doi: 10.1056/NEJMc2000644. N Engl J Med. 2020. PMID: 32294363 No abstract available.
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