Publication:
Pembrolizumab Plus Ipilimumab or Placebo for Metastatic Non-Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score >= 50%: Randomized, Double-Blind Phase III KEYNOTE-598 Study

dc.contributor.authorsBoyer, Michael; Sendur, Mehmet A. N.; Rodriguez-Abreu, Delvys; Park, Keunchil; Lee, Dae Ho; Cicin, Irfan; Yumuk, Perran Fulden; Orlandi, Francisco J.; Leal, Ticiana A.; Molinier, Olivier; Soparattanapaisarn, Nopadol; Langleben, Adrian; Califano, Raffaele; Medgyasszay, Balazs; Hsia, Te-Chun; Otterson, Gregory A.; Xu, Lu; Piperdi, Bilal; Samkari, Ayman; Reck, Martin
dc.date.accessioned2022-03-14T09:59:53Z
dc.date.accessioned2026-01-11T18:25:21Z
dc.date.available2022-03-14T09:59:53Z
dc.date.issued2021-07-20
dc.description.abstractPURPOSE Pembrolizumab monotherapy is standard first-line therapy for metastatic non-small-cell lung cancer (NSCLC) with programmed death ligand 1 (PD-L1) tumor proportion score (TPS) >= 50% without actionable driver mutations. It is not known whether adding ipilimumab to pembrolizumab improves efficacy over pembrolizumab alone in this population. METHODS In the randomized, double-blind, phase III KEYNOTE-598 trial (ClinicalTrials.gov identifier: ), eligible patients with previously untreated metastatic NSCLC with PD-L1 TPS >= 50% and no sensitizing EGFR or ALK aberrations were randomly allocated 1:1 to ipilimumab 1 mg/kg or placebo every 6 weeks for up to 18 doses; all participants received pembrolizumab 200 mg every 3 weeks for up to 35 doses. Primary end points were overall survival and progression-free survival. RESULTS Of the 568 participants, 284 were randomly allocated to each group. Median overall survival was 21.4 months for pembrolizumab-ipilimumab versus 21.9 months for pembrolizumab-placebo (hazard ratio, 1.08; 95% CI, 0.85 to 1.37; P = .74). Median progression-free survival was 8.2 months for pembrolizumab-ipilimumab versus 8.4 months for pembrolizumab-placebo (hazard ratio, 1.06; 95% CI, 0.86 to 1.30; P = .72). Grade 3-5 adverse events occurred in 62.4% of pembrolizumab-ipilimumab recipients versus 50.2% of pembrolizumab-placebo recipients and led to death in 13.1% versus 7.5%. The external data and safety monitoring committee recommended that the study be stopped for futility and that participants discontinue ipilimumab and placebo. CONCLUSION Adding ipilimumab to pembrolizumab does not improve efficacy and is associated with greater toxicity than pembrolizumab monotherapy as first-line treatment for metastatic NSCLC with PD-L1 TPS >= 50% and no targetable EGFR or ALK aberrations. These data do not support use of pembrolizumab-ipilimumab in place of pembrolizumab monotherapy in this population. (C) 2021 by American Society of Clinical Oncology
dc.identifier.doi10.1200/JCO.20.03579
dc.identifier.eissn1527-7755
dc.identifier.issn0732-183X
dc.identifier.pubmed33513313
dc.identifier.urihttps://hdl.handle.net/11424/243853
dc.identifier.wosWOS:000708089900003
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartofJOURNAL OF CLINICAL ONCOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCOMBINED NIVOLUMAB
dc.subjectRESPONSE CRITERIA
dc.subjectCHEMOTHERAPY
dc.subjectSURVIVAL
dc.titlePembrolizumab Plus Ipilimumab or Placebo for Metastatic Non-Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score >= 50%: Randomized, Double-Blind Phase III KEYNOTE-598 Study
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage+
oaire.citation.issue21
oaire.citation.startPage2327
oaire.citation.titleJOURNAL OF CLINICAL ONCOLOGY
oaire.citation.volume39

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