In contrast to prior studies, adding bevacizumab to erlotinib provides no progression-free survival benefit for treatment-naive patients.
Identifying mechanisms to delay development of resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in EGFR-mutated non–small-cell lung cancer (NSCLC) is a high clinical research priority.
To test whether adding the antiangiogenic agent bevacizumab to standard first-line therapy with erlotinib improves outcomes in this setting, investigators conducted a multicenter, randomized, phase II trial in which 88 treatment-naive, stage 4 NSCLC patients with EGFR mutations (del exon 19, exon 21 L858) were assigned to erlotinib (150 mg daily) with or without bevacizumab (15 mg/kg every 3 weeks). Of these patients 85% were white, 70% were women, 55% were never smokers, and 67% had deletion exon 19 EGFR mutation.
At medi…
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