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目前关于黑色素瘤免疫治疗耐药的知识以及潜在的预测和预后生物标志物

英文原题:Current knowledge about immunotherapy resistance for melanoma and potential predictive and prognostic biomarkers.

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Current knowledge about immunotherapy resistance for melanoma and potential predictive and prognostic biomarkers.

PubMed 2024/05/13(内容时间) Cancer Drug Resist Q1 · IF 7.6(JCR 2025)

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中文摘要

黑色素瘤每年仍有数千例新诊断病例,其侵袭性使得康复充满挑战,尤其是对于III/IV期不可切除的黑色素瘤患者。免疫治疗作为希望的灯塔出现,站在晚期黑色素瘤治疗的前沿。本综述深入探讨了各种免疫治疗策略,主要包括细胞因子免疫治疗、过继细胞治疗、免疫检查点抑制剂和疫苗。其中,免疫检查点抑制剂,特别是抗程序性细胞死亡-1(PD-1)和抗细胞毒性T淋巴细胞抗原-4(CTLA-4)抗体,成为领先策略。然而,相当一部分黑色素瘤患者对这些抑制剂仍无反应,凸显了对有效生物标志物的需求。高效的生物标志物有潜力通过促进为黑色素瘤患者设计个性化治疗来彻底改变治疗格局。这篇综合性综述重点介绍了黑色素瘤免疫治疗的最新进展以及近期研究努力核心的潜在生物标志物。

展开英文摘要原文

Melanoma still reaches thousands of new diagnoses per year, and its aggressiveness makes recovery challenging, especially for those with stage III/IV unresectable melanoma. Immunotherapy, emerging as a beacon of hope, stands at the forefront of treatments for advanced melanoma.

This review delves into the various immunotherapeutic strategies, prominently featuring cytokine immunotherapy, adoptive cell therapy, immune checkpoint inhibitors, and vaccinations. Among these, immune checkpoint inhibitors, notably anti-programmed cell death-1 (PD-1) and anti-cytotoxic T lymphocyte antigen-4 (CTLA-4) antibodies, emerge as the leading strategy.

However, a significant subset of melanoma patients remains unresponsive to these inhibitors, underscoring the need for potent biomarkers. Efficient biomarkers have the potential to revolutionize the therapeutic landscape by facilitating the design of personalized treatments for patients with melanoma. This comprehensive review highlights the latest advancements in melanoma immunotherapy and potential biomarkers at the epicenter of recent research endeavors.

论文信息

作者
Song L、Yang Y、Tian X
单位
Wenzhou Municipal Key Laboratory for Applied Biomedical and Bio-pharmaceutical Informatics, Wenzhou-Kean University, Wenzhou 325060, Zhejiang, China.China
文献类型
综述
期刊
Cancer drug resistance (Alhambra, Calif.)2024
原文标识
PubMed 38835341 · DOI 10.20517/cdr.2023.150