Pembrolizumab monotherapy versus chemotherapy in platinum-pretreated, recurrent or metastatic nasopharyngeal cancer (KEYNOTE-122): an open-label, randomized, phase III trial
dc.contributor.author | Chan A.T.C. | |
dc.contributor.author | Lee V.H.F. | |
dc.contributor.author | Hong R.L. | |
dc.contributor.author | Ahn M.J. | |
dc.contributor.author | Chong W.Q. | |
dc.contributor.author | Kim S.B. | |
dc.contributor.author | Ho G.F. | |
dc.contributor.author | Caguioa P.B. | |
dc.contributor.author | Ngamphaiboon N. | |
dc.contributor.author | Ho C. | |
dc.contributor.author | Aziz M.A.S.A. | |
dc.contributor.author | Ng Q.S. | |
dc.contributor.author | Yen C.J. | |
dc.contributor.author | Soparattanapaisarn N. | |
dc.contributor.author | Ngan R.K.C. | |
dc.contributor.author | Kho S.K. | |
dc.contributor.author | Tiambeng M.L.A. | |
dc.contributor.author | Yun T. | |
dc.contributor.author | Sriuranpong V. | |
dc.contributor.author | Algazi A.P. | |
dc.contributor.author | Cheng A. | |
dc.contributor.author | Massarelli E. | |
dc.contributor.author | Swaby R.F. | |
dc.contributor.author | Saraf S. | |
dc.contributor.author | Yuan J. | |
dc.contributor.author | Siu L.L. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-05-19T08:23:41Z | |
dc.date.available | 2023-05-19T08:23:41Z | |
dc.date.issued | 2023-03-01 | |
dc.description.abstract | Background: 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.citation | Annals of Oncology Vol.34 No.3 (2023) , 251-261 | |
dc.identifier.doi | 10.1016/j.annonc.2022.12.007 | |
dc.identifier.eissn | 15698041 | |
dc.identifier.issn | 09237534 | |
dc.identifier.pmid | 36535566 | |
dc.identifier.scopus | 2-s2.0-85147365199 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/82374 | |
dc.rights.holder | SCOPUS | |
dc.subject | Medicine | |
dc.title | Pembrolizumab monotherapy versus chemotherapy in platinum-pretreated, recurrent or metastatic nasopharyngeal cancer (KEYNOTE-122): an open-label, randomized, phase III trial | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147365199&origin=inward | |
oaire.citation.endPage | 261 | |
oaire.citation.issue | 3 | |
oaire.citation.startPage | 251 | |
oaire.citation.title | Annals of Oncology | |
oaire.citation.volume | 34 | |
oairecerif.author.affiliation | Ramathibodi Hospital | |
oairecerif.author.affiliation | Siriraj Hospital | |
oairecerif.author.affiliation | Hospital Umum Sarawak | |
oairecerif.author.affiliation | National Cheng Kung University Hospital | |
oairecerif.author.affiliation | National Taiwan University Hospital | |
oairecerif.author.affiliation | University of Santo Tomas, Manila | |
oairecerif.author.affiliation | National Cancer Center, Gyeonggi | |
oairecerif.author.affiliation | National Cancer Centre, Singapore | |
oairecerif.author.affiliation | Universiti Malaya | |
oairecerif.author.affiliation | Prince of Wales Hospital Hong Kong | |
oairecerif.author.affiliation | University of California, San Francisco | |
oairecerif.author.affiliation | King Chulalongkorn Memorial Hospital | |
oairecerif.author.affiliation | Samsung Medical Center, Sungkyunkwan University | |
oairecerif.author.affiliation | University of Toronto | |
oairecerif.author.affiliation | Queen Elizabeth Hospital Hong Kong | |
oairecerif.author.affiliation | Princess Margaret Hospital Hong Kong | |
oairecerif.author.affiliation | Pantai Holdings Sdn Bhd | |
oairecerif.author.affiliation | The University of British Columbia | |
oairecerif.author.affiliation | Merck & Co., Inc. | |
oairecerif.author.affiliation | City of Hope National Med Center | |
oairecerif.author.affiliation | The University of Hong Kong | |
oairecerif.author.affiliation | University of Ulsan College of Medicine | |
oairecerif.author.affiliation | National University Cancer Institute | |
oairecerif.author.affiliation | Cardinal Santos Medical Center |