The objective response rate was only 8.2%.
We do not know whether oral epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) can be sequenced after patients with non–small-cell lung cancer (NSCLC) experience disease progression during treatment with these agents.
Now, investigators in Japan have conducted a single-arm, open-label, phase II study (LUX-Lung 4) of the irreversible EGFR TKI afatinib (50 mg per day) in 61 evaluable patients with stage IIIB–IV NSCLC (45 were EGFR-mutation–positive). All patients had progressed after receiving ≥12 weeks of the reversible EGFR TKIs erlotinib, gefitinib, or both. Results were as follows:
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