First-line nivolumab plus ipilimumab in advanced non-small-cell lung cancer (CheckMate 568): Outcomes by programmed death ligand 1 and tumor mutational burden as biomarkers Journal Article


Authors: Ready, N.; Hellmann, M. D.; Awad, M. M.; Otterson, G. A.; Gutierrez, M.; Gainor, J. F.; Borghaei, H.; Jolivet, J.; Horn, L.; Mates, M.; Brahmer, J.; Rabinowitz, I.; Reddy, P. S.; Chesney, J.; Orcutt, J.; Spigel, D. R.; Reck, M.; O'Byrne, K. J.; Paz-Ares, L.; Hu, W.; Zerba, K.; Li, X.; Lestini, B.; Geese, W. J.; Szustakowski, J. D.; Green, G.; Chang, H.; Ramalingam, S. S.
Article Title: First-line nivolumab plus ipilimumab in advanced non-small-cell lung cancer (CheckMate 568): Outcomes by programmed death ligand 1 and tumor mutational burden as biomarkers
Abstract: PURPOSE CheckMate 568 is an open-label phase II trial that evaluated the efficacy and safety of nivolumab plus low-dose ipilimumab as first-line treatment of advanced/metastatic non-small-cell lung cancer (NSCLC). We assessed the association of efficacy with programmed death ligand 1 (PD-L1) expression and tumor mutational burden (TMB). PATIENTS AND METHODS Two hundred eighty-eight patients with previously untreated, recurrent stage IIIB/IV NSCLC received nivolumab 3 mg/kg every 2 weeks plus ipilimumab 1 mg/kg every 6 weeks. The primary end point was objective response rate (ORR) in patients with 1% or more and less than 1% tumor PD-L1 expression. Efficacy on the basis of TMB (FoundationOne CDx assay) was a secondary end point. RESULTS Of treated patients with tumor available for testing, 252 patients (88%) of 288 were evaluable for PD-L1 expression and 98 patients (82%) of 120 for TMB. ORR was 30% overall and 41% and 15% in patients with 1% or greater and less than 1% tumor PD-L1 expression, respectively. ORR increased with higher TMB, plateauing at 10 or more mutations/megabase (mut/Mb). Regardless of PD-L1 expression, ORRs were higher in patients with TMB of 10 or more mut/Mb (n = 48: PD-L1, >= 1%, 48%; PD-L1, < 1%, 47%) versus TMB of fewer than 10 mut/Mb (n = 50: PD-L1, >= 1%, 18%; PD-L1, < 1%, 5%), and progression-free survival was longer in patients with TMB of 10 or more mut/Mb versus TMB of fewer than 10 mut/Mb (median, 7.1 v 2.6 months). Grade 3 to 4 treatment-related adverse events occurred in 29% of patients. CONCLUSION Nivolumab plus low-dose ipilimumab was effective and tolerable as a first-line treatment of advanced/metastatic NSCLC. TMB of 10 or more mut/Mb was associated with improved response and prolonged progression-free survival in both tumor PD-L1 expression 1% or greater and less than 1% subgroups and was thus identified as a potentially relevant cutoff in the assessment of TMB as a biomarker for first-line nivolumab plus ipilimumab. (C) 2019 by American Society of Clinical Oncology
Keywords: docetaxel; pd-1; multicenter; landscape; blockade; stage iv; open-label
Journal Title: Journal of Clinical Oncology
Volume: 37
Issue: 12
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2019-04-20
Start Page: 992
End Page: 1000
Language: English
ACCESSION: WOS:000466717700007
DOI: 10.1200/jco.18.01042
PROVIDER: wos
PUBMED: 30785829
PMCID: PMC6494267
Notes: Article -- Source: Wos
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  1. Matthew David Hellmann
    411 Hellmann