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Safety and Efficacy Results of a Phase I, Open-Label Study of Concurrent and Delayed Nivolumab in Combination With nab -Paclitaxel and Carboplatin in Advanced Non-small Cell Lung Cancer.

Authors :
Goldman JW
Waterhouse DM
George B
O'Dwyer PJ
Bhore R
Banerjee S
Lyons L
Louis CU
Ong TJ
Kelly K
Source :
Frontiers in oncology [Front Oncol] 2019 Nov 26; Vol. 9, pp. 1256. Date of Electronic Publication: 2019 Nov 26 (Print Publication: 2019).
Publication Year :
2019

Abstract

Introduction: Multicenter, phase I study of concurrent and delayed nivolumab plus nab -paclitaxel/carboplatin in advanced non-small cell lung cancer (NSCLC). Methods: Chemotherapy-naive patients with advanced NSCLC (ineligible for potentially curative radiation or surgery) received nab -paclitaxel 100 mg/m <superscript>2</superscript> (days 1, 8, 15) and carboplatin area under the curve 6 (day 1) intravenously every 21 days (first 4 cycles); nivolumab 5 mg/kg was administered intravenously (day 15) beginning in cycle 1 (concurrent) or cycle 3 (delayed) in separate cohorts and continued beyond the 4 chemotherapy cycles. The primary objective was to assess safety. Secondary objectives were to assess tolerability and explore antitumor activity. Results: All 32 patients received chemotherapy; 20 of 22 and 6 of 10 patients also received concurrent or delayed nivolumab, respectively. No dose-limiting toxicities were reported in the concurrent cohort; 1 dose-limiting toxicity was reported in the delayed cohort. In the concurrent cohort, 20 patients (91%) had ≥1 grade 3/4 treatment-emergent adverse event (TEAE), and 7 (32%) discontinued treatment due to TEAEs. In the delayed cohort, all patients had ≥1 grade 3/4 TEAE, and 2 (20%) discontinued due to TEAEs. The median progression-free and overall survival, respectively, were 10.5 and 29.3 months in the concurrent cohort and 4.1 and 8.2 months in the delayed cohort. Conclusions: The safety profile of the combination was consistent with that of individual agents and generally similar in the 2 cohorts. Efficacy outcomes in the concurrent cohort, but not in the delayed cohort, were encouraging and support the rationale for concurrent administration of nivolumab with nab -paclitaxel/carboplatin for the treatment of advanced NSCLC. Clinical Trial Registration: www.ClinicalTrials.gov, identifier: NCT02309177.<br /> (Copyright © 2019 Goldman, Waterhouse, George, O'Dwyer, Bhore, Banerjee, Lyons, Louis, Ong and Kelly.)

Details

Language :
English
ISSN :
2234-943X
Volume :
9
Database :
MEDLINE
Journal :
Frontiers in oncology
Publication Type :
Academic Journal
Accession number :
31850192
Full Text :
https://doi.org/10.3389/fonc.2019.01256