Pembrolizumab With or Without Chemotherapy in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: Updated Results of the Phase III KEYNOTE-048 Study

dc.contributor.authorHarrington K.J.
dc.contributor.authorBurtness B.
dc.contributor.authorGreil R.
dc.contributor.authorSoulières D.
dc.contributor.authorTahara M.
dc.contributor.authorDe Castro G.
dc.contributor.authorPsyrri A.
dc.contributor.authorBrana I.
dc.contributor.authorBasté N.
dc.contributor.authorNeupane P.
dc.contributor.authorBratland Å.
dc.contributor.authorFuereder T.
dc.contributor.authorHughes B.G.M.
dc.contributor.authorMesia R.
dc.contributor.authorNgamphaiboon N.
dc.contributor.authorRordorf T.
dc.contributor.authorWan Ishak W.Z.
dc.contributor.authorLin J.
dc.contributor.authorGumuscu B.
dc.contributor.authorSwaby R.F.
dc.contributor.authorRischin D.
dc.contributor.otherMahidol University
dc.date.accessioned2023-05-19T07:36:01Z
dc.date.available2023-05-19T07:36:01Z
dc.date.issued2023-02-01
dc.description.abstractPURPOSEPembrolizumab and pembrolizumab-chemotherapy demonstrated efficacy in recurrent/metastatic head and neck squamous cell carcinoma in KEYNOTE-048. Post hoc analysis of long-term efficacy and progression-free survival on next-line therapy (PFS2) is presented.METHODSPatients were randomly assigned (1:1:1) to pembrolizumab, pembrolizumab-chemotherapy, or cetuximab-chemotherapy. Efficacy was evaluated in programmed death ligand 1 (PD-L1) combined positive score (CPS) ≥ 20, CPS ≥ 1, and total populations, with no multiplicity or alpha adjustment.RESULTSThe median study follow-up was 45.0 months (interquartile range, 41.0-49.2; n = 882). At data cutoff (February 18, 2020), overall survival improved with pembrolizumab in the PD-L1 CPS ≥ 20 (hazard ratio [HR], 0.61; 95% CI, 0.46 to 0.81) and CPS ≥ 1 populations (HR, 0.74; 95% CI, 0.61 to 0.89) and was noninferior in the total population (HR, 0.81; 95% CI, 0.68 to 0.97). Overall survival improved with pembrolizumab-chemotherapy in the PD-L1 CPS ≥ 20 (HR, 0.62; 95% CI, 0.46 to 0.84), CPS ≥ 1 (HR, 0.64; 95% CI, 0.53 to 0.78), and total (HR, 0.71; 95% CI, 0.59 to 0.85) populations. The objective response rate on second-course pembrolizumab was 27.3% (3 of 11). PFS2 improved with pembrolizumab in the PD-L1 CPS ≥ 20 (HR, 0.64; 95% CI, 0.48 to 0.84) and CPS ≥ 1 (HR, 0.79; 95% CI, 0.66 to 0.95) populations and with pembrolizumab-chemotherapy in the PD-L1 CPS ≥ 20 (HR, 0.64; 95% CI, 0.48 to 0.86), CPS ≥ 1 (HR, 0.66; 95% CI, 0.55 to 0.81), and total (HR, 0.73; 95% CI, 0.61 to 0.88) populations. PFS2 was similar after pembrolizumab and longer after pembrolizumab-chemotherapy on next-line taxanes and shorter after pembrolizumab and similar after pembrolizumab-chemotherapy on next-line nontaxanes.CONCLUSIONWith a 4-year follow-up, first-line pembrolizumab and pembrolizumab-chemotherapy continued to demonstrate survival benefit versus cetuximab-chemotherapy in recurrent/metastatic head and neck squamous cell carcinoma. Patients responded well to subsequent treatment after pembrolizumab-based therapy.
dc.identifier.citationJournal of Clinical Oncology Vol.41 No.4 (2023) , 790-802
dc.identifier.doi10.1200/JCO.21.02508
dc.identifier.eissn15277755
dc.identifier.issn0732183X
dc.identifier.pmid36219809
dc.identifier.scopus2-s2.0-85147094382
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/81670
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titlePembrolizumab With or Without Chemotherapy in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: Updated Results of the Phase III KEYNOTE-048 Study
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147094382&origin=inward
oaire.citation.endPage802
oaire.citation.issue4
oaire.citation.startPage790
oaire.citation.titleJournal of Clinical Oncology
oaire.citation.volume41
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationVall d‘Hebron Institut de Oncologia
oairecerif.author.affiliationOslo Universitetssykehus
oairecerif.author.affiliationPeter Maccallum Cancer Centre
oairecerif.author.affiliationThe University of Queensland
oairecerif.author.affiliationYale Cancer Center
oairecerif.author.affiliationUniversiti Malaya
oairecerif.author.affiliationNational and Kapodistrian University of Athens
oairecerif.author.affiliationUniversity of Melbourne
oairecerif.author.affiliationUniversitatsSpital Zurich
oairecerif.author.affiliationThe Royal Marsden NHS Foundation Trust
oairecerif.author.affiliationParacelsus Medizinische Privatuniversitat
oairecerif.author.affiliationMedizinische Universität Wien
oairecerif.author.affiliationNational Cancer Center Hospital East
oairecerif.author.affiliationCentre Hospitalier de L'Universite de Montreal
oairecerif.author.affiliationUniversidade de São Paulo
oairecerif.author.affiliationMerck & Co., Inc.
oairecerif.author.affiliationUniversity of Kansas Medical Center
oairecerif.author.affiliationIGTP
oairecerif.author.affiliationCenter for Clinical Cancer and Immunology Trials

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