Tislelizumab for the treatment of advanced esophageal squamous cell carcinoma

被引:0
作者
Shiraishi, Kazuhiro [1 ]
Yamamoto, Shun [1 ]
Kato, Ken [1 ]
机构
[1] Natl Canc Ctr, Esophageal Med Oncol, Dept Head & Neck, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
关键词
Esophageal cancer; esophageal squamous cell carcinoma; immune checkpoint inhibitor; tislelizumab; RATIONALE-306; RATIONALE-302; PHASE-II EVALUATION; PD-1; BLOCKADE; CANCER; CHEMOTHERAPY; 5-FLUOROURACIL; CISPLATIN; INFUSION; SURVIVAL; PLACEBO; TUMORS;
D O I
10.1080/14796694.2025.2495542
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advanced esophageal squamous cell carcinoma (ESCC) patients had poor prognosis and few effective drugs based on the randomized controlled trials (RCTs). In such a circumstance, recent RCTs have shown the clinical efficacy of immune checkpoint inhibitors (ICIs) as first- or second-line treatment for advanced ESCC patients. Tislelizumab is one of the anti-Programmed-Death-1 (PD-1) antibodies; at first, tislelizumab monotherapy showed clinical efficacy as a second-line treatment for advanced ESCC patients based on the results of the RATIONALE-302 trial. Since then, tislelizumab plus doublet chemotherapy has shown superiority in overall survival compared to doublet chemotherapy for untreated advanced ESCC patients in the RATIONALE-306 trial. In this review, we share the overview of the development of tislelizumab and discuss the future perspectives on ICIs for advanced ESCC patients. In our opinion, tislelizumab plus doublet chemotherapy is one of the first-line standard treatments for advanced ESCC patients regardless of Programmed cell Death ligand 1 expression. Some other ICI-containing treatments showed clinical efficacy for untreated ESCC patients; we need further investigation to select these treatments appropriately.
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页数:9
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