4.6 Article

Randomized Phase 2 Study of Osimertinib Plus Bevacizumab Versus Osimertinib for Untreated Patients With Nonsquamous NSCLC Harboring EGFR Mutations: WJOG9717L Study

Journal

JOURNAL OF THORACIC ONCOLOGY
Volume 17, Issue 9, Pages 1098-1108

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtho.2022.05.006

Keywords

Non-small cell lung cancer; EGFR mutation; Osimertinib; Bevacizumab

Funding

  1. AstraZeneca K.K

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This study evaluated the efficacy and safety of osimertinib plus bevacizumab in previously untreated patients with advanced nonsquamous NSCLC harboring EGFR-sensitizing mutations. The results showed no significant improvement in progression-free survival with osimertinib plus bevacizumab compared to osimertinib monotherapy. Adverse events were slightly higher in the osimertinib plus bevacizumab group.
Introduction: To evaluate the efficacy and safety of osimertinib plus bevacizumab for previously untreated patients with advanced nonsquamous NSCLC harboring EGFR-sensitizing mutations. Methods: We conducted a randomized, open-label, phase 2 study at 21 institutions in Japan. Previously untreated patients with advanced nonsquamous NSCLC harboring EGFR-sensitizing mutations received either osimertinib (80 mg, daily) plus bevacizumab (15 mg/kg, every 3 wk) or osimertinib monotherapy, and were stratified according to sex, stage, and EGFR mutation status. The primary end point was progression-free survival (PFS) in the intention-to-treat population, assessed by means of blinded, independent central radiologic review. Results: Between January 2018 and September 2018, a total of 122 patients were enrolled (osimertinib + bevacizumab arm, 61 patients; osimertinib monotherapy arm, 61 patients). At a median follow-up duration of 19.8 months, the median PFS was 22.1 months for osimertinib plus bevacizumab and 20.2 months for osimertinib monotherapy, with a hazard ratio of 0.862 (60% confidence interval: 0.700-1.060, 95% confidence interval: 0.531-1.397, one-sided stratified log-rank p = 0.213). Adverse events of grade 3 or worse were observed in 34 patients (56%) in the osimertinib plus bevacizumab arm and 29 (48%) in the osimertinib monotherapy arm. In addition, two (3%) and 11 patients (18%) experienced any grade pneumonitis, respectively, and grade 3 pneumonitis was observed in one patient (2%) in each arm. Conclusions: This study failed to exhibit the efficacy of osimertinib plus bevacizumab for improving the PFS among patients with nonsquamous NSCLC harboring EGFR mutations as first-line treatment. (C) 2022 International Association for the Study of Lung Cancer. Published by Elsevier Inc.

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