Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial

We evaluated the efficacy and safety of pembrolizumab in patients from Asia with previously treated advanced hepatocellular carcinoma (HCC).METHODSIn a double-blind, phase III trial, 453 patients with advanced HCC and progression during or after treatment with or intolerance to sorafenib or oxalipla...

Full description

Saved in:
Bibliographic Details
Main Authors: Qin, Shukui, Chen, Zhendong, Fang, Weijia, Ren, Zhenggang, Xu, Ruocai, Ryoo, Baek-Yeol, Meng, Zhiqiang, Bai, Yuxian, Chen, Xiaoming, Liu, Xiufeng, Xiao, Juxiang, Ho, Gwo Fuang, Mao, Yimin, Wang, Xin, Ying, Jieer, Li, Jianfeng, Zhong, Wenyan, Zhou, Yu, Siegel, Abby B., Hao, Chunyi
Format: Article
Published: American Society of Clinical Oncology 2023
Subjects:
Online Access:http://eprints.um.edu.my/38540/
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universiti Malaya
id my.um.eprints.38540
record_format eprints
spelling my.um.eprints.385402024-08-14T06:59:02Z http://eprints.um.edu.my/38540/ Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial Qin, Shukui Chen, Zhendong Fang, Weijia Ren, Zhenggang Xu, Ruocai Ryoo, Baek-Yeol Meng, Zhiqiang Bai, Yuxian Chen, Xiaoming Liu, Xiufeng Xiao, Juxiang Ho, Gwo Fuang Mao, Yimin Wang, Xin Ying, Jieer Li, Jianfeng Zhong, Wenyan Zhou, Yu Siegel, Abby B. Hao, Chunyi R Medicine RA Public aspects of medicine We evaluated the efficacy and safety of pembrolizumab in patients from Asia with previously treated advanced hepatocellular carcinoma (HCC).METHODSIn a double-blind, phase III trial, 453 patients with advanced HCC and progression during or after treatment with or intolerance to sorafenib or oxaliplatin-based chemotherapy were randomly assigned in a 2:1 ratio to receive pembrolizumab (200 mg) or placebo once every 3 weeks for <= 35 cycles plus best supportive care. The primary end point was overall survival (one-sided significance threshold, P = .0193 final analysis]). Secondary end points included progression-free survival (PFS) and objective response rate (ORR; one-sided significance threshold, P = .0134 and .0091, respectively second interim analysis]; RECIST version 1.1, by blinded independent central review).RESULTSMedian overall survival was longer in the pembrolizumab group than in the placebo group (14.6 v 13.0 months; hazard ratio for death, 0.79; 95% CI, 0.63 to 0.99; P = .0180). Median PFS was also longer in the pembrolizumab group than in the placebo group (2.6 v 2.3 months; hazard ratio for progression or death, 0.74; 95% CI, 0.60 to 0.92; P = .0032). ORR was greater in the pembrolizumab group (12.7% 95% CI, 9.1 to 17.0]) than in the placebo group (1.3% 95% CI, 0.2 to 4.6]; P < .0001). Treatment-related adverse events occurred in 66.9% of patients (grade 3, 12.0%; grade 4, 1.3%; grade 5, 1.0%) in the pembrolizumab group and 49.7% of patients (grade 3, 5.9%; grade 4, 0%; grade 5, 0%) in the placebo group.CONCLUSIONIn patients from Asia with previously treated advanced HCC, pembrolizumab significantly prolonged overall survival and PFS, and ORR was greater versus placebo. American Society of Clinical Oncology 2023-03 Article PeerReviewed Qin, Shukui and Chen, Zhendong and Fang, Weijia and Ren, Zhenggang and Xu, Ruocai and Ryoo, Baek-Yeol and Meng, Zhiqiang and Bai, Yuxian and Chen, Xiaoming and Liu, Xiufeng and Xiao, Juxiang and Ho, Gwo Fuang and Mao, Yimin and Wang, Xin and Ying, Jieer and Li, Jianfeng and Zhong, Wenyan and Zhou, Yu and Siegel, Abby B. and Hao, Chunyi (2023) Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial. Journal of Clinical Oncology, 41 (7). 1434+. ISSN 0732-183X, DOI https://doi.org/10.1200/JCO.22.00620 <https://doi.org/10.1200/JCO.22.00620>. 10.1200/JCO.22.00620
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
RA Public aspects of medicine
spellingShingle R Medicine
RA Public aspects of medicine
Qin, Shukui
Chen, Zhendong
Fang, Weijia
Ren, Zhenggang
Xu, Ruocai
Ryoo, Baek-Yeol
Meng, Zhiqiang
Bai, Yuxian
Chen, Xiaoming
Liu, Xiufeng
Xiao, Juxiang
Ho, Gwo Fuang
Mao, Yimin
Wang, Xin
Ying, Jieer
Li, Jianfeng
Zhong, Wenyan
Zhou, Yu
Siegel, Abby B.
Hao, Chunyi
Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
description We evaluated the efficacy and safety of pembrolizumab in patients from Asia with previously treated advanced hepatocellular carcinoma (HCC).METHODSIn a double-blind, phase III trial, 453 patients with advanced HCC and progression during or after treatment with or intolerance to sorafenib or oxaliplatin-based chemotherapy were randomly assigned in a 2:1 ratio to receive pembrolizumab (200 mg) or placebo once every 3 weeks for <= 35 cycles plus best supportive care. The primary end point was overall survival (one-sided significance threshold, P = .0193 final analysis]). Secondary end points included progression-free survival (PFS) and objective response rate (ORR; one-sided significance threshold, P = .0134 and .0091, respectively second interim analysis]; RECIST version 1.1, by blinded independent central review).RESULTSMedian overall survival was longer in the pembrolizumab group than in the placebo group (14.6 v 13.0 months; hazard ratio for death, 0.79; 95% CI, 0.63 to 0.99; P = .0180). Median PFS was also longer in the pembrolizumab group than in the placebo group (2.6 v 2.3 months; hazard ratio for progression or death, 0.74; 95% CI, 0.60 to 0.92; P = .0032). ORR was greater in the pembrolizumab group (12.7% 95% CI, 9.1 to 17.0]) than in the placebo group (1.3% 95% CI, 0.2 to 4.6]; P < .0001). Treatment-related adverse events occurred in 66.9% of patients (grade 3, 12.0%; grade 4, 1.3%; grade 5, 1.0%) in the pembrolizumab group and 49.7% of patients (grade 3, 5.9%; grade 4, 0%; grade 5, 0%) in the placebo group.CONCLUSIONIn patients from Asia with previously treated advanced HCC, pembrolizumab significantly prolonged overall survival and PFS, and ORR was greater versus placebo.
format Article
author Qin, Shukui
Chen, Zhendong
Fang, Weijia
Ren, Zhenggang
Xu, Ruocai
Ryoo, Baek-Yeol
Meng, Zhiqiang
Bai, Yuxian
Chen, Xiaoming
Liu, Xiufeng
Xiao, Juxiang
Ho, Gwo Fuang
Mao, Yimin
Wang, Xin
Ying, Jieer
Li, Jianfeng
Zhong, Wenyan
Zhou, Yu
Siegel, Abby B.
Hao, Chunyi
author_facet Qin, Shukui
Chen, Zhendong
Fang, Weijia
Ren, Zhenggang
Xu, Ruocai
Ryoo, Baek-Yeol
Meng, Zhiqiang
Bai, Yuxian
Chen, Xiaoming
Liu, Xiufeng
Xiao, Juxiang
Ho, Gwo Fuang
Mao, Yimin
Wang, Xin
Ying, Jieer
Li, Jianfeng
Zhong, Wenyan
Zhou, Yu
Siegel, Abby B.
Hao, Chunyi
author_sort Qin, Shukui
title Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
title_short Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
title_full Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
title_fullStr Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
title_full_unstemmed Pembrolizumab Versus Placebo as second-line therapy in patients From Asia with advanced hepatocellular carcinoma: A randomized, double-blind, phase III trial
title_sort pembrolizumab versus placebo as second-line therapy in patients from asia with advanced hepatocellular carcinoma: a randomized, double-blind, phase iii trial
publisher American Society of Clinical Oncology
publishDate 2023
url http://eprints.um.edu.my/38540/
_version_ 1809136911945564160