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Pembrolizumab monotherapy versus chemotherapy in platinum-pretreated, recurrent or metastatic nasopharyngeal cancer (KEYNOTE-122): an open-label, randomized, phase III trial.
Chan, A T C; Lee, V H F; Hong, R-L; Ahn, M-J; Chong, W Q; Kim, S-B; Ho, G F; Caguioa, P B; Ngamphaiboon, N; Ho, C; Aziz, M A S A; Ng, Q S; Yen, C-J; Soparattanapaisarn, N; Ngan, R K-C; Kho, S K; Tiambeng, M L A; Yun, T; Sriuranpong, V; Algazi, A P; Cheng, A; Massarelli, E; Swaby, R F; Saraf, S; Yuan, J; Siu, L L.
Affiliation
  • Chan ATC; State Key Laboratory in Translational Oncology, Sir YK Pao Centre for Cancer, The Chinese University of Hong Kong, Hong Kong, China. Electronic address: anthonytcchan@cuhk.edu.hk.
  • Lee VHF; Department of Clinical Oncology, The University of Hong Kong, Hong Kong, China.
  • Hong RL; National Taiwan University Hospital, Taipei, Taiwan.
  • Ahn MJ; Samsung Medical Centre, Seoul, South Korea.
  • Chong WQ; National University Cancer Institute, Singapore, Singapore.
  • Kim SB; Asan Medical Centre, University of Ulsan College of Medicine, Seoul, South Korea.
  • Ho GF; Clinical Oncology, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
  • Caguioa PB; St. Luke's Medical Center, University of Santo Tomas Faculty of Medicine and Surgery, Manila, Philippines.
  • Ngamphaiboon N; Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
  • Ho C; BC Cancer, University of British Columbia, Vancouver, Canada.
  • Aziz MASA; Gleneagles Penang Clinical Research Center, Gleneagles Hospital Penang, Penang, Malaysia.
  • Ng QS; National Cancer Centre Singapore, Singapore, Singapore.
  • Yen CJ; National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Soparattanapaisarn N; Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Ngan RK; Queen Elizabeth Hospital, Kowloon, Hong Kong, China.
  • Kho SK; Hospital Umum Sarawak, Kuching, Malaysia.
  • Tiambeng MLA; Cardinal Santos Medical Center, San Juan City, Philippines.
  • Yun T; National Cancer Center, Goyang-si, South Korea.
  • Sriuranpong V; Chulalongkorn University and the King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Algazi AP; UCSF, San Francisco, USA.
  • Cheng A; Princess Margaret Hospital, Hong Kong, China.
  • Massarelli E; City of Hope Comprehensive Cancer Center, Duarte, USA.
  • Swaby RF; Merck & Co., Inc., Rahway, USA.
  • Saraf S; Merck & Co., Inc., Rahway, USA.
  • Yuan J; Merck & Co., Inc., Rahway, USA.
  • Siu LL; Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
Ann Oncol ; 34(3): 251-261, 2023 03.
Article in En | MEDLINE | ID: mdl-36535566
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.
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Full text: 1 Database: MEDLINE Main subject: Platinum / Nasopharyngeal Neoplasms Type of study: Clinical_trials Limits: Humans Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Platinum / Nasopharyngeal Neoplasms Type of study: Clinical_trials Limits: Humans Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2023 Type: Article