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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

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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.
Issued Date
2023
A.T.C. Chan
V.H.F. Lee
R.-L. Hong
M.-J. Ahn
W.Q. Chong
S.-B. Kim
G.F. Ho
P.B. Caguioa
N. Ngamphaiboon
C. Ho
M.A.S.A. Aziz
Q.S. Ng
C.-J. Yen
N. Soparattanapaisarn
R.K.-C. Ngan
S.K. Kho
M.L.A. Tiambeng
T. Yun
V. Sriuranpong
A.P. Algazi
L.L. Siu
Type
Article
Keyword
immunotherapynasopharyngeal cancerpembrolizumabprogrammed death-1 (PD-1)
DOI
10.1016/j.annonc.2022.12.007
URI
https://oak.ulsan.ac.kr/handle/2021.oak/16575
Publisher
ANNALS OF ONCOLOGY
Language
영어
ISSN
0923-7534
Citation Volume
34
Citation Number
3
Citation Start Page
251
Citation End Page
261
Appears in Collections:
Medicine > Nursing
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