The trial did not meet its primary endpoint of noninferiority for gefitinib in terms of progression-free survival.
Four epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors are currently FDA-approved for EGFR-mutated non–small-cell lung cancer (NSCLC). In frontline EGFR-mutated patients, afatinib, gefitinib, and erlotinib are available, and osimertinib is approved for T790M patients. Gefitinib and erlotinib are also approved for salvage use in EGFR–wild-type NSCLC.
Now, the West Japan Oncology Group has conducted a multicenter, randomized, open-label, noninferiority, phase III trial (WJOG 5108L), in which 561 previously chemotherapy-treated patients with advanced lung adenocarcinoma (71% had EGFR mutations) were randomized to receive gefitinib or erlotinib. The primary endpoint was progression-free survival (PFS) noninferiority with gefitin…
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