Ontology highlight
ABSTRACT: Background
Patients with advanced squamous-cell non-small-cell lung cancer (NSCLC) who have disease progression during or after first-line chemotherapy have limited treatment options. This randomized, open-label, international, phase 3 study evaluated the efficacy and safety of nivolumab, a fully human IgG4 programmed death 1 (PD-1) immune-checkpoint-inhibitor antibody, as compared with docetaxel in this patient population.Methods
We randomly assigned 272 patients to receive nivolumab, at a dose of 3 mg per kilogram of body weight every 2 weeks, or docetaxel, at a dose of 75 mg per square meter of body-surface area every 3 weeks. The primary end point was overall survival.Results
The median overall survival was 9.2 months (95% confidence interval [CI], 7.3 to 13.3)
SUBMITTER: Brahmer J
PROVIDER: S-EPMC4681400 | biostudies-literature | 2015 Jul
REPOSITORIES: biostudies-literature