Five-Year Follow-Up of Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: Results From the CA209-003 Study

Scott Gettinger(Dana-Farber Cancer Institute), Leora Horn(Dana-Farber Cancer Institute), David M. Jackman(Dana-Farber Cancer Institute), David R. Spigel(Dana-Farber Cancer Institute), Scott Antonia(Dana-Farber Cancer Institute), Matthew D. Hellmann(Dana-Farber Cancer Institute), John D. Powderly(Dana-Farber Cancer Institute), Rebecca S. Heist(Dana-Farber Cancer Institute), Lecia V. Sequist(Dana-Farber Cancer Institute), David C. Smith(Dana-Farber Cancer Institute), Philip D. Leming(Dana-Farber Cancer Institute), William J. Geese(Dana-Farber Cancer Institute), Dennis J. Yoon(Dana-Farber Cancer Institute), Ang Li(Dana-Farber Cancer Institute), Julie R. Brahmer(Dana-Farber Cancer Institute)
Journal of Clinical Oncology
March 23, 2018
Cited by 747

Abstract

Purpose In two phase III studies, nivolumab, a programmed death-1 (PD-1) inhibitor antibody, improved overall survival (OS) versus docetaxel in pretreated advanced non-small-cell lung cancer (NSCLC). We report 5-year follow-up results from an early phase I study of nivolumab in this patient population and describe characteristics of 5-year survivors. Patients and Methods Patients with pretreated, advanced NSCLC received nivolumab 1, 3, or 10 mg/kg every 2 weeks in 8-week cycles for up to 96 weeks. OS from the time of first dose was estimated by the Kaplan-Meier method. Results The estimated 5-year OS rate was 16% for all treated patients (N = 129); 5-year OS rates were similar for squamous (16%) and nonsquamous (15%) NSCLC. Of 16 5-year survivors, most (88%) were known current or former smokers. Of 10 5-year survivors with quantifiable PD-1 ligand 1 expression, 70% had ≥ 1% PD-1 ligand 1 expression at baseline. Twelve 5-year survivors (75%) achieved a partial response to nivolumab per Response Evaluation Criteria in Solid Tumors, version 1.0, and two each (12%) had stable disease and progressive disease as best response. Nine 5-year survivors (56%) completed the maximum 96 weeks of nivolumab; four (25%) discontinued owing to adverse events and three (19%) owing to disease progression. As of a November 2016 database lock, 12 5-year survivors (75%) received no subsequent therapy and were without evidence of progressive disease at last follow-up. Conclusions Nivolumab treatment resulted in long-term OS and durable responses in a proportion of patients with pretreated advanced NSCLC. Long-term survivors had diverse baseline and on-treatment characteristics.


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