Pembrolizumab with or without chemotherapy in recurrent or metastatic head and neck squamous cell carcinoma: 5-year follow-up from the randomized phase III KEYNOTE-048 study
| dc.contributor.author | Tahara M. | |
| dc.contributor.author | Greil R. | |
| dc.contributor.author | Rischin D. | |
| dc.contributor.author | Harrington K.J. | |
| dc.contributor.author | Burtness B. | |
| dc.contributor.author | de Castro G. | |
| dc.contributor.author | Psyrri A. | |
| dc.contributor.author | Braña I. | |
| 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 | Mesía R. | |
| dc.contributor.author | Ngamphaiboon N. | |
| dc.contributor.author | Rordorf T. | |
| dc.contributor.author | Ishak W.Z.W. | |
| dc.contributor.author | Lin J. | |
| dc.contributor.author | Gumuscu B. | |
| dc.contributor.author | Lerman N. | |
| dc.contributor.author | Soulières D. | |
| dc.contributor.correspondence | Tahara M. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2025-04-28T18:07:04Z | |
| dc.date.available | 2025-04-28T18:07:04Z | |
| dc.date.issued | 2025-05-15 | |
| dc.description.abstract | Background: Pembrolizumab monotherapy and pembrolizumab-chemotherapy demonstrated superior overall survival (OS) versus cetuximab-chemotherapy (EXTREME) in the primary analysis of the phase III KEYNOTE-048 study of recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) in the first-line setting. We report updated data with 5 years of follow-up. Methods: Adults with previously untreated R/M HNSCC incurable by local therapy were randomly assigned 1:1:1 to pembrolizumab, pembrolizumab plus chemotherapy, or EXTREME. The primary endpoints were OS and progression-free survival (PFS). Results: Overall, 882 participants were assigned to pembrolizumab, pembrolizumab-chemotherapy, or EXTREME. Median study follow-up was 69.2 months (pembrolizumab) and 68.6 months (pembrolizumab-chemotherapy). Median OS remained longer for pembrolizumab versus EXTREME in the programmed cell death ligand 1 (PD-L1) combined positive score (CPS) ≥ 20 (HR, 0.61; 95 % CI, 0.46–0.81) and CPS ≥ 1 populations (HR, 0.74; 95 % CI, 0.61–0.89), and similar in the total population (HR, 0.82; 95 % CI, 0.69–0.97). Pembrolizumab-chemotherapy prolonged median OS in the PD-L1 CPS ≥ 20 (HR, 0.63; 95 % CI, 0.47–0.84), CPS ≥ 1 (HR, 0.65; 95 % CI, 0.53–0.79), and total (HR, 0.72; 95 % CI, 0.60–0.86) populations. The 5-year OS rate in the total population was 14.4 % for pembrolizumab versus 6.5 % for EXTREME and 16.0 % for pembrolizumab-chemotherapy versus 5.2 % for EXTREME. There was no clinically meaningful difference in PFS among pembrolizumab, pembrolizumab-chemotherapy, or EXTREME groups in any populations. Conclusions: These 5-year follow-up results support the use of pembrolizumab and pembrolizumab-chemotherapy as first-line standards of care for R/M HNSCC. Clinical Trial Information: NCT02358031. Prior Presentation: Presented at the European Society for Medical Oncology Congress, September 9–13, 2022. | |
| dc.identifier.citation | European Journal of Cancer Vol.221 (2025) | |
| dc.identifier.doi | 10.1016/j.ejca.2025.115395 | |
| dc.identifier.eissn | 18790852 | |
| dc.identifier.issn | 09598049 | |
| dc.identifier.scopus | 2-s2.0-105002856892 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/109806 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Biochemistry, Genetics and Molecular Biology | |
| dc.subject | Medicine | |
| dc.title | Pembrolizumab with or without chemotherapy in recurrent or metastatic head and neck squamous cell carcinoma: 5-year follow-up from the randomized phase III KEYNOTE-048 study | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105002856892&origin=inward | |
| oaire.citation.title | European Journal of Cancer | |
| oaire.citation.volume | 221 | |
| 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 | Universiti Malaya | |
| oairecerif.author.affiliation | National and Kapodistrian University of Athens | |
| oairecerif.author.affiliation | Royal Brisbane and Women's Hospital | |
| oairecerif.author.affiliation | Allgemeines KrankenHaus Wien | |
| oairecerif.author.affiliation | UniversitatsSpital Zurich | |
| oairecerif.author.affiliation | Yale School of Medicine | |
| oairecerif.author.affiliation | Institute Catala Oncologia | |
| oairecerif.author.affiliation | Paracelsus Medizinische Privatuniversitat | |
| oairecerif.author.affiliation | National Cancer Center Hospital East | |
| oairecerif.author.affiliation | The Institute of Cancer Research | |
| oairecerif.author.affiliation | Centre Hospitalier de L'Université de Montréal | |
| oairecerif.author.affiliation | Universidade de São Paulo | |
| oairecerif.author.affiliation | Merck & Co., Inc. | |
| oairecerif.author.affiliation | University of Kansas Medical Center |
