Research status on immunotherapy trials of gastric cancer

被引:5
|
作者
Liang, Chao [1 ]
Wu, Heng-Miao [2 ]
Yu, Wei-Ming [1 ]
Chen, Wei [3 ]
机构
[1] Lihuili Hosp, Dept Gen Surg, Ningbo Med Ctr, Ningbo 315040, Zhejiang, Peoples R China
[2] Ningbo Univ, Ningbo Med Ctr, Lihuili Hosp, Ningbo 315040, Zhejiang, Peoples R China
[3] Tongde Hosp Zhejiang Prov, Zhejiang Acad Tradit Chinese Med, Canc Inst Integrated Tradit Chinese & Western Med, 234 Gucui Rd, Hangzhou 310012, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastric cancer; Immunotherapy; Clinical trial; Immune checkpoint inhibitor; Neoadjuvant therapy; IMMUNE-RELATED RESPONSE; PLUS PEMBROLIZUMAB; SINGLE-ARM; END-POINTS; TUMOR; COMBINATION; THERAPY; PD-1; BLOCKADE; 1ST-LINE;
D O I
10.12998/wjcc.v9.i21.5782
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The breakthrough of immune checkpoint inhibitor (ICI) therapy has created extensive opportunities for cancer immunotherapy. Especially, the block of programmed death-1/programmed death ligand 1 (PD-L1) axis using ICIs has become a new therapeutic strategy to treat advanced gastric cancer (GC). However, in the past decade, single-arm and randomized trials for single-drug ICI therapy showed that the therapeutic effect was not satisfactory, including clinical trials for advanced GC. However, after selecting suitable predictive biomarkers and developing a combination of anti-angiogenic targeted drugs and other chemotherapeutic drugs, the objective response rate and progression-free survival of patients with gastric cancer were improved significantly. The United States Food and Drug Administration has approved treatment with pembrolizumab for patients with advanced GC with PD-L1 expression or microsatellite instability-high/mismatch repair deficiency. In this review, the updated data from the latest trial results of combination immunotherapy for GC are presented. Based on the outcome of combination therapy, we discuss its possible molecular mechanism and summarize effective predictive biomarkers. We also discuss possible problems stemming from results of other clinical trials of ICI treatment and propose other directions for ICI therapy.
引用
收藏
页码:5782 / 5793
页数:12
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