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Overall Survival and Long-Term Safety of Nivolumab (Anti-Programmed Death 1 Antibody, BMS-936558, ONO-4538) in Patients With Previously Treated Advanced Non-Small-Cell Lung Cancer.


ABSTRACT:

Purpose

Programmed death 1 is an immune checkpoint that suppresses antitumor immunity. Nivolumab, a fully human immunoglobulin G4 programmed death 1 immune checkpoint inhibitor antibody, was active and generally well tolerated in patients with advanced solid tumors treated in a phase I trial with expansion cohorts. We report overall survival (OS), response durability, and long-term safety in patients with non-small-cell lung cancer (NSCLC) receiving nivolumab in this trial.

Patients and methods

Patients (N = 129) with heavily pretreated advanced NSCLC received nivolumab 1, 3, or 10 mg/kg intravenously once every 2 weeks in 8-week cycles for up to 96 weeks. Tumor burden was assessed by RECIST (version 1.0) after each cycle.

Results

Median OS across doses was 9.9 months; 1-, 2-, and 3-year OS rates were 42%, 24%, and 18%, respectively, across doses and 56%, 42%, and 27%, respectively, at the 3-mg/kg dose (n = 37) chosen for further clinical development. Among 22 patients (17%) with objective responses, estimated median response duration was 17.0 months. An additional six patients (5%) had unconventional immune-pattern responses. Response rates were similar in squamous and nonsquamous NSCLC. Eighteen responding patients discontinued nivolumab for reasons other than progressive disease; nine (50%) of those had responses lasting > 9 months after their last dose. Grade 3 to 4 treatment-related adverse events occurred in 14% of patients. Three treatment-related deaths (2% of patients) occurred, each associated with pneumonitis.

Conclusion

Nivolumab monotherapy produced durable responses and encouraging survival rates in patients with heavily pretreated NSCLC. Randomized clinical trials with nivolumab in advanced NSCLC are ongoing.

SUBMITTER: Gettinger SN 

PROVIDER: S-EPMC4672027 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Publications

Overall Survival and Long-Term Safety of Nivolumab (Anti-Programmed Death 1 Antibody, BMS-936558, ONO-4538) in Patients With Previously Treated Advanced Non-Small-Cell Lung Cancer.

Gettinger Scott N SN   Horn Leora L   Gandhi Leena L   Spigel David R DR   Antonia Scott J SJ   Rizvi Naiyer A NA   Powderly John D JD   Heist Rebecca S RS   Carvajal Richard D RD   Jackman David M DM   Sequist Lecia V LV   Smith David C DC   Leming Philip P   Carbone David P DP   Pinder-Schenck Mary C MC   Topalian Suzanne L SL   Hodi F Stephen FS   Sosman Jeffrey A JA   Sznol Mario M   McDermott David F DF   Pardoll Drew M DM   Sankar Vindira V   Ahlers Christoph M CM   Salvati Mark M   Wigginton Jon M JM   Hellmann Matthew D MD   Kollia Georgia D GD   Gupta Ashok K AK   Brahmer Julie R JR  

Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20150420 18


<h4>Purpose</h4>Programmed death 1 is an immune checkpoint that suppresses antitumor immunity. Nivolumab, a fully human immunoglobulin G4 programmed death 1 immune checkpoint inhibitor antibody, was active and generally well tolerated in patients with advanced solid tumors treated in a phase I trial with expansion cohorts. We report overall survival (OS), response durability, and long-term safety in patients with non-small-cell lung cancer (NSCLC) receiving nivolumab in this trial.<h4>Patients a  ...[more]

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