Show simple item record

dc.contributor.authorHarrington, KJ
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, BGM
dc.contributor.authorMesia, R
dc.contributor.authorNgamphaiboon, N
dc.contributor.authorRordorf, T
dc.contributor.authorWan Ishak, WZ
dc.contributor.authorLin, J
dc.contributor.authorGumuscu, B
dc.contributor.authorSwaby, RF
dc.contributor.authorRischin, D
dc.coverage.spatialUnited States
dc.date.accessioned2022-12-23T09:57:26Z
dc.date.available2022-12-23T09:57:26Z
dc.date.issued2023-02-01
dc.identifier.citationJournal of Clinical Oncology, 2022, pp. JCO2102508 -
dc.identifier.issn0732-183X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5625
dc.identifier.eissn1527-7755
dc.identifier.eissn1527-7755
dc.identifier.doi10.1200/JCO.21.02508
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.formatPrint-Electronic
dc.format.extentJCO2102508 -
dc.languageeng
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartofJournal of Clinical Oncology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
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.typeJournal Article
dcterms.dateAccepted2022-07-06
dc.date.updated2022-12-23T09:56:44Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1200/JCO.21.02508
rioxxterms.licenseref.startdate2022-10-11
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36219809
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR/ImmNet
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1200/jco.21.02508
icr.researchteamTargeted Therapy
dc.contributor.icrauthorHarrington, Kevin
icr.provenanceDeposited by Mr Arek Surman on 2022-12-23. Deposit type is initial. No. of files: 1. Files: jco.21.02508.pdf


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by-nc-nd/4.0/
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/