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.author | Harrington K.J. | |
dc.contributor.author | Burtness B. | |
dc.contributor.author | Greil R. | |
dc.contributor.author | Soulières D. | |
dc.contributor.author | Tahara M. | |
dc.contributor.author | De Castro G. | |
dc.contributor.author | Psyrri A. | |
dc.contributor.author | Brana I. | |
dc.contributor.author | Basté N. | |
dc.contributor.author | Neupane P. | |
dc.contributor.author | Bratland Å. | |
dc.contributor.author | Fuereder T. | |
dc.contributor.author | Hughes B.G.M. | |
dc.contributor.author | Mesia R. | |
dc.contributor.author | Ngamphaiboon N. | |
dc.contributor.author | Rordorf T. | |
dc.contributor.author | Wan Ishak W.Z. | |
dc.contributor.author | Lin J. | |
dc.contributor.author | Gumuscu B. | |
dc.contributor.author | Swaby R.F. | |
dc.contributor.author | Rischin D. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-05-19T07:36:01Z | |
dc.date.available | 2023-05-19T07:36:01Z | |
dc.date.issued | 2023-02-01 | |
dc.description.abstract | PURPOSEPembrolizumab 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.citation | Journal of Clinical Oncology Vol.41 No.4 (2023) , 790-802 | |
dc.identifier.doi | 10.1200/JCO.21.02508 | |
dc.identifier.eissn | 15277755 | |
dc.identifier.issn | 0732183X | |
dc.identifier.pmid | 36219809 | |
dc.identifier.scopus | 2-s2.0-85147094382 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/81670 | |
dc.rights.holder | SCOPUS | |
dc.subject | Biochemistry, Genetics and Molecular Biology | |
dc.title | 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.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147094382&origin=inward | |
oaire.citation.endPage | 802 | |
oaire.citation.issue | 4 | |
oaire.citation.startPage | 790 | |
oaire.citation.title | Journal of Clinical Oncology | |
oaire.citation.volume | 41 | |
oairecerif.author.affiliation | Ramathibodi Hospital | |
oairecerif.author.affiliation | Vall d‘Hebron Institut de Oncologia | |
oairecerif.author.affiliation | Oslo Universitetssykehus | |
oairecerif.author.affiliation | Peter Maccallum Cancer Centre | |
oairecerif.author.affiliation | The University of Queensland | |
oairecerif.author.affiliation | Yale Cancer Center | |
oairecerif.author.affiliation | Universiti Malaya | |
oairecerif.author.affiliation | National and Kapodistrian University of Athens | |
oairecerif.author.affiliation | University of Melbourne | |
oairecerif.author.affiliation | UniversitatsSpital Zurich | |
oairecerif.author.affiliation | The Royal Marsden NHS Foundation Trust | |
oairecerif.author.affiliation | Paracelsus Medizinische Privatuniversitat | |
oairecerif.author.affiliation | Medizinische Universität Wien | |
oairecerif.author.affiliation | National Cancer Center Hospital East | |
oairecerif.author.affiliation | Centre Hospitalier de L'Universite de Montreal | |
oairecerif.author.affiliation | Universidade de São Paulo | |
oairecerif.author.affiliation | Merck & Co., Inc. | |
oairecerif.author.affiliation | University of Kansas Medical Center | |
oairecerif.author.affiliation | IGTP | |
oairecerif.author.affiliation | Center for Clinical Cancer and Immunology Trials |