Pembrolizumab monotherapy versus chemotherapy in platinum-pretreated, recurrent or metastatic nasopharyngeal cancer (KEYNOTE-122): an open-label, randomized, phase III trial

dc.contributor.authorChan A.T.C.
dc.contributor.authorLee V.H.F.
dc.contributor.authorHong R.L.
dc.contributor.authorAhn M.J.
dc.contributor.authorChong W.Q.
dc.contributor.authorKim S.B.
dc.contributor.authorHo G.F.
dc.contributor.authorCaguioa P.B.
dc.contributor.authorNgamphaiboon N.
dc.contributor.authorHo C.
dc.contributor.authorAziz M.A.S.A.
dc.contributor.authorNg Q.S.
dc.contributor.authorYen C.J.
dc.contributor.authorSoparattanapaisarn N.
dc.contributor.authorNgan R.K.C.
dc.contributor.authorKho S.K.
dc.contributor.authorTiambeng M.L.A.
dc.contributor.authorYun T.
dc.contributor.authorSriuranpong V.
dc.contributor.authorAlgazi A.P.
dc.contributor.authorCheng A.
dc.contributor.authorMassarelli E.
dc.contributor.authorSwaby R.F.
dc.contributor.authorSaraf S.
dc.contributor.authorYuan J.
dc.contributor.authorSiu L.L.
dc.contributor.otherMahidol University
dc.date.accessioned2023-05-19T08:23:41Z
dc.date.available2023-05-19T08:23:41Z
dc.date.issued2023-03-01
dc.description.abstractBackground: Pembrolizumab previously demonstrated robust antitumor activity and manageable safety in a phase Ib study of patients with heavily pretreated, programmed death ligand 1 (PD-L1)-positive, recurrent or metastatic nasopharyngeal carcinoma (NPC). The phase III KEYNOTE-122 study was conducted to further evaluate pembrolizumab versus chemotherapy in patients with platinum-pretreated, recurrent and/or metastatic NPC. Final analysis results are presented. Patients and methods: KEYNOTE-122 was an open-label, randomized study conducted at 29 sites, globally. Participants with platinum-pretreated recurrent and/or metastatic NPC were randomly assigned (1 : 1) to pembrolizumab or chemotherapy with capecitabine, gemcitabine, or docetaxel. Randomization was stratified by liver metastasis (present versus absent). The primary endpoint was overall survival (OS), analyzed in the intention-to-treat population using the stratified log-rank test (superiority threshold, one-sided P = 0.0187). Safety was assessed in the as-treated population. Results: Between 5 May 2016 and 28 May 2018, 233 participants were randomly assigned to treatment (pembrolizumab, n = 117; chemotherapy, n = 116); Most participants (86.7%) received study treatment in the second-line or later setting. Median time from randomization to data cut-off (30 November 2020) was 45.1 months (interquartile range, 39.0-48.8 months). Median OS was 17.2 months [95% confidence interval (CI) 11.7-22.9 months] with pembrolizumab and 15.3 months (95% CI 10.9-18.1 months) with chemotherapy [hazard ratio, 0.90 (95% CI 0.67-1.19; P = 0.2262)]. Grade 3-5 treatment-related adverse events occurred in 12 of 116 participants (10.3%) with pembrolizumab and 49 of 112 participants (43.8%) with chemotherapy. Three treatment-related deaths occurred: 1 participant (0.9%) with pembrolizumab (pneumonitis) and 2 (1.8%) with chemotherapy (pneumonia, intracranial hemorrhage). Conclusion: Pembrolizumab did not significantly improve OS compared with chemotherapy in participants with platinum-pretreated recurrent and/or metastatic NPC but did have manageable safety and a lower incidence of treatment-related adverse events.
dc.identifier.citationAnnals of Oncology Vol.34 No.3 (2023) , 251-261
dc.identifier.doi10.1016/j.annonc.2022.12.007
dc.identifier.eissn15698041
dc.identifier.issn09237534
dc.identifier.pmid36535566
dc.identifier.scopus2-s2.0-85147365199
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/82374
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titlePembrolizumab monotherapy versus chemotherapy in platinum-pretreated, recurrent or metastatic nasopharyngeal cancer (KEYNOTE-122): an open-label, randomized, phase III trial
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147365199&origin=inward
oaire.citation.endPage261
oaire.citation.issue3
oaire.citation.startPage251
oaire.citation.titleAnnals of Oncology
oaire.citation.volume34
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationHospital Umum Sarawak
oairecerif.author.affiliationNational Cheng Kung University Hospital
oairecerif.author.affiliationNational Taiwan University Hospital
oairecerif.author.affiliationUniversity of Santo Tomas, Manila
oairecerif.author.affiliationNational Cancer Center, Gyeonggi
oairecerif.author.affiliationNational Cancer Centre, Singapore
oairecerif.author.affiliationUniversiti Malaya
oairecerif.author.affiliationPrince of Wales Hospital Hong Kong
oairecerif.author.affiliationUniversity of California, San Francisco
oairecerif.author.affiliationKing Chulalongkorn Memorial Hospital
oairecerif.author.affiliationSamsung Medical Center, Sungkyunkwan University
oairecerif.author.affiliationUniversity of Toronto
oairecerif.author.affiliationQueen Elizabeth Hospital Hong Kong
oairecerif.author.affiliationPrincess Margaret Hospital Hong Kong
oairecerif.author.affiliationPantai Holdings Sdn Bhd
oairecerif.author.affiliationThe University of British Columbia
oairecerif.author.affiliationMerck & Co., Inc.
oairecerif.author.affiliationCity of Hope National Med Center
oairecerif.author.affiliationThe University of Hong Kong
oairecerif.author.affiliationUniversity of Ulsan College of Medicine
oairecerif.author.affiliationNational University Cancer Institute
oairecerif.author.affiliationCardinal Santos Medical Center

Files

Collections