Advances in the Use of Immune Checkpoint Inhibitors for Colorectal Cancer Treatment.

IF 2.8 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2025-10-15 eCollection Date: 2025-01-01 DOI:10.2147/OTT.S551204
Jianing Li, Tong Fu, Zhu Wen, Jiahao Liang, Yanzhi Qiu, Kaiqing Li, Jiamin Yang, Ying Tong, Hongbo Cai
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引用次数: 0

Abstract

Purpose: Colorectal cancer (CRC) is a highly prevalent malignant tumor worldwide, and the emergence of immune checkpoint inhibitors (ICIs) has changed CRC immunotherapy. This systematic review aims to provide a comprehensive overview of registered clinical trials on ICIs in CRC worldwide, with a focus on major molecular targets, combination therapy strategies, geographic distribution patterns, and future directions for precision immunotherapy.

Methods: All clinical trials related to ICIs in CRC were retrieved. Trials were screened according to inclusion and exclusion criteria, and core information such as trial phase, conducting country, mechanism targets, and combination therapy, was systematically organized for retrospective and trend analyses.

Results: A total of 1,479 eligible clinical trials were included. There has been a steady increase in the number of registered trials, with Phase II trials being the most numerous. The United States and China lead globally in the number of trials reported. Key research targets included PD-1, PD-L1, CTLA-4, and molecules related to the tumor microenvironment. Combination therapies involving ICIs, anti-angiogenic agents, and targeted drugs across multiple pathways emerged as a new research focus.

Conclusion: ICIs have driven the development of precision immunotherapy for CRC, and multi-target combination therapies hold promise for improving outcomes. However, clinical translation and efficacy improvements remain challenging. Future studies should focus on the mechanisms involved and accumulating clinical data to guide more effective immunotherapy strategies.

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免疫检查点抑制剂在结直肠癌治疗中的应用进展
目的:结直肠癌(Colorectal cancer, CRC)是世界范围内高度流行的恶性肿瘤,免疫检查点抑制剂(immune checkpoint inhibitors, ICIs)的出现改变了结直肠癌的免疫治疗。本系统综述旨在全面概述全球结直肠癌中已注册的ICIs临床试验,重点关注主要分子靶点、联合治疗策略、地理分布模式和精准免疫治疗的未来方向。方法:检索所有与结直肠癌中ICIs相关的临床试验。根据纳入和排除标准筛选试验,系统整理试验阶段、开展国、机制靶点、联合治疗等核心信息,进行回顾性分析和趋势分析。结果:共纳入1479项符合条件的临床试验。注册试验的数量稳步增加,其中II期试验数量最多。美国和中国在报告的试验数量方面处于全球领先地位。重点研究靶点包括PD-1、PD-L1、CTLA-4以及与肿瘤微环境相关的分子。包括ICIs、抗血管生成药物和靶向药物在内的多种途径的联合治疗成为新的研究热点。结论:ICIs推动了CRC精准免疫治疗的发展,多靶点联合治疗有望改善预后。然而,临床转化和疗效改善仍然具有挑战性。未来的研究应侧重于相关机制和积累临床数据,以指导更有效的免疫治疗策略。
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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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