Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer
Isabelle Ray‐Coquard(Université Claude Bernard Lyon 1), Patricia Pautier(Université Claude Bernard Lyon 1), Sandro Pignata(Université Claude Bernard Lyon 1), David Pérol(Université Claude Bernard Lyon 1), Antonio González-Martı́n(Université Claude Bernard Lyon 1), Regina Berger(Université Claude Bernard Lyon 1), Keiichi Fujiwara(Université Claude Bernard Lyon 1), Ignace Vergote(Université Claude Bernard Lyon 1), Nicoletta Colombo(Université Claude Bernard Lyon 1), Johanna Mäenpää(Université Claude Bernard Lyon 1), Frédèric Selle(Université Claude Bernard Lyon 1), Jalid Sehouli(Université Claude Bernard Lyon 1), Domenica Lorusso(Université Claude Bernard Lyon 1), Eva María Guerra Alia(Université Claude Bernard Lyon 1), Alexander Reinthaller(Université Claude Bernard Lyon 1), Shoji Nagao(Université Claude Bernard Lyon 1), Claudia Lefeuvre‐Plesse(Université Claude Bernard Lyon 1), Ulrich Canzler(Université Claude Bernard Lyon 1), Giovanni Scambia(Université Claude Bernard Lyon 1), Alain Lortholary(Université Claude Bernard Lyon 1), Frederik Marmé(Université Claude Bernard Lyon 1), Pierre Combe(Université Claude Bernard Lyon 1), Nikolaus de Gregorio(Université Claude Bernard Lyon 1), Manuel Rodrigues(Université Claude Bernard Lyon 1), Paul Buderath(Université Claude Bernard Lyon 1), Coraline Dubot(Université Claude Bernard Lyon 1), Alexander Burges(Université Claude Bernard Lyon 1), Benoît You(Université Claude Bernard Lyon 1), Éric Pujade-Lauraine(Université Claude Bernard Lyon 1), Philipp Harter(Université Claude Bernard Lyon 1)
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Abstract
BACKGROUND: mutation status is unknown. METHODS: 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: 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: mutation. (Funded by ARCAGY Research and others; PAOLA-1 ClinicalTrials.gov number, NCT02477644.).
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