Adding bevacizumab to cisplatin and etoposide improved progression-free survival, but not overall survival, the primary outcome.
Patients with extensive-stage small-cell lung cancer (ES-SCLC) have limited treatment options beyond first-line platinum-etoposide therapy. Early phase II trials demonstrated improvement in outcomes in this setting with the addition of bevacizumab, an antiangiogenic agent.
Now, Italian investigators have conducted a multicenter, randomized phase III trial, in which 205 treatment-naive ES-SCLC patients received cisplatin and etoposide with or without bevacizumab for 6 cycles. Nonprogressors in the bevacizumab arm received maintenance therapy for a maximum of 18 cycles.
At a median follow-up of 34.9 months, the addition of bevacizumab significantly improved median progression-free survival (PFS; 6.7 vs 5.7 months; hazard ratio, 0.72; P=0.03), b…
Reviewing Author
DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
RoyaltiesUpToDate
Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb
DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
RoyaltiesUpToDate
Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb