微卫星稳定型结直肠癌的免疫治疗:克服耐药性和探索新的治疗策略。

IF 2.1 Q2 GASTROENTEROLOGY & HEPATOLOGY
Annals of Coloproctology Pub Date : 2026-02-01 Epub Date: 2026-02-19 DOI:10.3393/ac.2025.01354.0193
Sun Young Kim
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引用次数: 0

摘要

微卫星稳定型(MSS)结直肠癌(CRC)占所有CRC病例的85%至95%,是癌症免疫治疗时代的重大治疗挑战。与对免疫检查点抑制剂表现出显著反应的微卫星不稳定性高肿瘤不同,由于肿瘤突变负担低、t细胞浸润最小和免疫抑制肿瘤微环境,MSS CRC表现出深刻的耐药性。本文回顾了MSS CRC免疫治疗试验的现状,包括最近报道的stella -303研究,讨论了新兴的预测性生物标志物,如肿瘤突变负担、免疫评分免疫检查点(Immunoscore- ic)和人工智能驱动的工具,如Lunit SCOPE,并探讨了克服免疫耐药的创新策略,包括下一代抗细胞毒性t淋巴细胞相关蛋白4 (anti-CTLA-4)抗体。程序性细胞死亡配体1 (PD-L1)/白细胞介素-2 (IL-2)双特异性抗体、cd47靶向策略、疫苗和嵌合抗原受体T (CAR-T)细胞治疗。了解这些不断发展的策略对于在这一具有挑战性的患者群体中推进精确免疫治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy for microsatellite-stable colorectal cancer: overcoming resistance and exploring novel therapeutic strategies.

Microsatellite-stable (MSS) colorectal cancer (CRC), comprising 85% to 95% of all CRC cases, represents a significant therapeutic challenge in the era of cancer immunotherapy. Unlike microsatellite instability-high tumors that demonstrate remarkable responses to immune checkpoint inhibitors, MSS CRC exhibits profound resistance due to low tumor mutational burden, minimal T-cell infiltration, and an immunosuppressive tumor microenvironment. This article reviews the current landscape of immunotherapy trials in MSS CRC, including the recently reported STELLAR-303 study, discusses emerging predictive biomarkers such as tumor mutational burden, Immunoscore Immune Checkpoint (Immunoscore-IC), and artificial intelligence-driven tools like Lunit SCOPE, and explores innovative strategies to overcome immune resistance, including next-generation anti-cytotoxic T-lymphocyte-associated protein-4 (anti-CTLA-4) antibodies, programmed cell death-ligand 1 (PD-L1)/interleukin-2 (IL-2) bispecific antibodies, CD47-targeting strategies, vaccines, and chimeric antigen receptor T (CAR-T) cell therapy. Understanding these evolving strategies is critical for advancing precision immunotherapy in this challenging patient population.

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来源期刊
CiteScore
3.30
自引率
3.20%
发文量
73
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