Overall survival was longer and toxicity was lower with nivolumab than with standard docetaxel in pretreated patients.
Limited advances have been made in second-line treatment of patients with advanced squamous-cell non–small cell lung cancer (SCC-NSCLC) since the introduction of docetaxel. In phase I and II studies, nivolumab — an IgG4 programmed death 1 (PD-1) immune-checkpoint–inhibitor antibody — demonstrated activity in previously treated SCC-NSCLC patients.
To further test the safety and efficacy of nivolumab versus docetaxel in this setting, investigators conducted an industry-funded, international, randomized, phase III trial (CheckMate 017) involving 272 patients with advanced SCC-NSCLC who experienced disease progression with prior chemotherapy. Patients received nivolumab (3 mg/kg every 2 weeks) or docetaxel (75 mg/m2 every 3 weeks). Results were …
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