Present and prospect of transarterial chemoembolization combined with tyrosine kinase inhibitor and PD-1 inhibitor for unresectable hepatocellular carcinoma

被引:1
|
作者
Zhang, Rui [1 ]
Liu, Yan-Hui [2 ]
Li, Yu [3 ]
Li, Nan-Nan [4 ]
Li, Zheng [5 ]
机构
[1] Anhui Med Univ, Peoples Hosp Hefei 2, Dept Pharm, Hefei Hosp, Hefei 230011, Anhui, Peoples R China
[2] Anhui Prov Childrens Hosp, Dept Clin Pharm, Hefei 230000, Anhui, Peoples R China
[3] Taihe Cty Peoples Hosp Anhui Prov, Dept Pharm, Fuyang 236600, Anhui, Peoples R China
[4] Univ Sci & Technol China, Affiliated Hosp 1, Hefei 230001, Anhui Province, Peoples R China
[5] Jiangsu Normal Univ, Coll Hlth Sci, Jiangsu Engn Res Ctr Cardiovasc Drugs Targeting En, Sch Life Sci, 101 Shanghai Rd, Xuzhou 221000, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Transarterial chemoembolization; Multi-targeted tyrosine kinase inhibitor; Programmed cell death protein-1 inhibitor; Unresectable hepatocellular carcinoma; Mechanism; ENDOTHELIAL GROWTH-FACTOR; SORAFENIB; IMMUNOTHERAPY; EXPRESSION; THERAPY;
D O I
10.4251/wjgo.v16.i11.4315
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this editorial, we comment on the article (World J Gastrointest Oncol 2024; 16: 1236-1247), which is a retrospective study of transarterial chemoembolization (TACE) combined with multi-targeted tyrosine kinase inhibitor (TKI) and programmed cell death protein-1 (PD-1) inhibitor for the treatment of unresectable hepatocellular carcinoma (HCC). Herein, we focus specifically on the mechanisms of this triple therapy, administration sequence and selection of each medication, and implications for future clinical trials. Based on the interaction mechanisms between medications, the triple therapy of TACE + TKI + PD-1 is proposed to complement the deficiency of each monotherapy, and achieve synergistic antitumor effects. Although this triple therapy has been evaluated by several retrospective trials, it is still controversial whether the triple therapy achieves better clinical benefits, due to the flawed study design and heterogeneity in medications. In addition, the administration sequence, which may greatly affect the clinical benefit, needs to be fully considered at clinical decision-making for obtaining better prognosis. We hope that this editorial could contribute to the design and optimization of future trials.
引用
收藏
页数:7
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