Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/195805
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dc.contributor.authorHarrington, Kevin J.-
dc.contributor.authorBurtness, Barbara-
dc.contributor.authorGreil, Richard-
dc.contributor.authorSoulières, Denis-
dc.contributor.authorTahara, Makoto-
dc.contributor.authorCastro, Gilberto de-
dc.contributor.authorPsyrri, Amanda-
dc.contributor.authorBraña, Irene-
dc.contributor.authorBasté, Neus-
dc.contributor.authorNeupane, Prakash-
dc.contributor.authorBratland, Åse-
dc.contributor.authorFuereder, Thorsten-
dc.contributor.authorHughes, Brett G.M.-
dc.contributor.authorMesía Nin, Ricard-
dc.contributor.authorNgamphaiboon, Nuttapong-
dc.contributor.authorRordorf, Tamara-
dc.contributor.authorIshak, Wan Zamaniah Wan-
dc.contributor.authorLin, Jiaxin-
dc.contributor.authorGumuscu, Burak-
dc.contributor.authorSwaby, Ramona F.-
dc.contributor.authorRischin, Danny-
dc.date.accessioned2023-03-22T15:59:46Z-
dc.date.available2023-04-11T05:10:31Z-
dc.date.issued2022-10-11-
dc.identifier.issn0732-183X-
dc.identifier.urihttp://hdl.handle.net/2445/195805-
dc.description.abstractPurpose: Pembrolizumab 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. Methods: Patients 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. Results: The 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. Conclusion: With 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.format.extent13 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1200/JCO.21.02508-
dc.relation.ispartofJournal of Clinical Oncology, 2022, vol. 41, num. 4, p. 790-802-
dc.relation.urihttps://doi.org/10.1200/JCO.21.02508-
dc.rights(c) American Society of Clinical Oncology, 2022-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationQuimioteràpia-
dc.subject.classificationCàncer de cap-
dc.subject.classificationCàncer de coll-
dc.subject.classificationAnticossos monoclonals-
dc.subject.otherChemotherapy-
dc.subject.otherHead cancer-
dc.subject.otherNeck cancer-
dc.subject.otherMonoclonal antibodies-
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.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec732810-
dc.date.updated2023-03-22T15:59:46Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid36219809-
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)

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