Comparative efficacy and tolerability of targeted and immunotherapy combined with chemotherapy as first-line treatment for advanced gastric cancer: a Bayesian network meta-analysis

被引:4
|
作者
Liu, Shu [1 ]
Wong, Heung Yan [1 ]
Xie, Li [1 ]
Kim, Yoojin [2 ]
Shu, Danhua [3 ]
Zheng, Beishi [4 ]
Liu, Naxin [5 ]
Xing, Chungen [6 ]
Chen, Xiaolei [5 ]
Dong, Qiantong [5 ,6 ]
机构
[1] City Univ Hong Kong, Dept Biomed Sci, Kowloon Tong, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Jockey Club Coll Vet Med & Life Sci, Kowloon Tong, Hong Kong, Peoples R China
[3] Queensland Univ Technol, Fac Hlth, Sch Biomed Sci, Brisbane, Qld, Australia
[4] Woodhull Med & Mental Hlth Ctr, Internal Med Dept, Brooklyn, NY USA
[5] Wenzhou Med Univ, Affiliated Hosp 1, Dept Gastrointestinal Surg, Wenzhou, Peoples R China
[6] Soochow Univ, Affiliated Hosp 2, Dept Gen Surg, Suzhou, Jiangsu, Peoples R China
关键词
ADVANCED ESOPHAGOGASTRIC CANCER; RANDOMIZED PHASE-II; DOUBLE-BLIND; GASTROESOPHAGEAL JUNCTION; OPEN-LABEL; PLUS OXALIPLATIN; ADVANCED ESOPHAGEAL; CAPECITABINE; ADENOCARCINOMA; CISPLATIN;
D O I
10.1038/s41598-022-24426-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The use of target agents and immune checkpoint inhibitors have changed the treatment landscape for AGC in the first-line setting. However, the crosswise comparison between each regimen is rare. Therefore, we estimated the efficacy and safety of targeted therapy or immunotherapy with chemotherapy in AGC patients as the first-line treatment. Included studies were divided into "average" or "specific positivity" group according to whether the patients were selected by a certain pathological expression. We conducted a Bayesian network meta-analysis for all regimens in both groups. In average group, no regimen showed significant improvements in overall survival (OS) and progression free survival (PFS), while pembrolizumab and nivolumab combined with chemotherapy were ranked first and second respectively without an obvious safety difference. In specific positivity group, zolbetuximab plus chemotherapy significantly prolonged OS (HR 0.53, 95% CI 0.36-0.79) and PFS (HR 0.45, 95% CI 0.25-0.81). The top three regimens were zolbetuximab-chemotherapy, trastuzumab plus pertuzuma-chemotherapy and nivolumab-chemotherapy respectively, with no significant safety risk. For average patients, immune checkpoint inhibitor PD-1 plus chemotherapy will be the promising regimen. For patients with overexpression of CLDN18.2, zolbetuximab combined with chemotherapy comes with greater survival benefits, while for patients who have PD-L1 expression with no HER-2 or CLDN18.2 positivity, additional immune checkpoint inhibitor of PD-1 will be a good considered option.
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页数:18
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