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解析并克服黑色素瘤的抗 PD-1 耐药性:机制、生物标志物开发和治疗策略的全面综述。

Deciphering and overcoming Anti-PD-1 resistance in Melanoma: A comprehensive review of Mechanisms, biomarker Developments, and therapeutic strategies.

机构信息

Shanghai Skin Disease Hospital, Shanghai Clinical College of Dermatology, Fifth Clinical Medical College, Anhui Medical University, Shanghai 200443, China.

Shanghai Skin Disease Hospital, Institute of Dermatology, School of Medicine, Tongji University, Shanghai 200443, China.

出版信息

Int Immunopharmacol. 2024 May 10;132:111989. doi: 10.1016/j.intimp.2024.111989. Epub 2024 Apr 8.

DOI:10.1016/j.intimp.2024.111989
PMID:38583243
Abstract

Worldwide, tens of thousands of people die from melanoma each year, making it the most frequently fatal form of cutaneous cancer. Immunotherapeutic advancements, particularly with anti-PD-1 medications, have significantly enhanced treatment outcomes over recent decades. With the broad application of anti-PD-1 therapies, insights into the mechanisms of resistance have evolved. Despite the development of combination treatments and early predictive biomarkers, a comprehensive synthesis of these advancements is absent in the current literature. This review underscores the prevailing knowledge of anti-PD-1 resistance mechanisms and underscores the critical role of robust predictive biomarkers in stratifying patients for targeted combinations of anti-PD-1 and other conventional or innovative therapeutic approaches. Additionally, we offer insights that may shape future melanoma treatment strategies.

摘要

全世界每年有数万人死于黑色素瘤,使其成为最常见的致命皮肤癌。免疫治疗的进步,特别是抗 PD-1 药物的应用,在最近几十年显著改善了治疗效果。随着抗 PD-1 治疗的广泛应用,对耐药机制的认识也在不断发展。尽管联合治疗和早期预测生物标志物的发展,但目前的文献中缺乏对这些进展的全面综合。本综述强调了抗 PD-1 耐药机制的现有知识,并强调了强大的预测生物标志物在为患者分层以进行抗 PD-1 与其他常规或创新治疗方法的靶向联合治疗方面的关键作用。此外,我们还提供了可能影响未来黑色素瘤治疗策略的见解。

相似文献

1
Deciphering and overcoming Anti-PD-1 resistance in Melanoma: A comprehensive review of Mechanisms, biomarker Developments, and therapeutic strategies.解析并克服黑色素瘤的抗 PD-1 耐药性:机制、生物标志物开发和治疗策略的全面综述。
Int Immunopharmacol. 2024 May 10;132:111989. doi: 10.1016/j.intimp.2024.111989. Epub 2024 Apr 8.
2
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Radiological dynamics and SITC-defined resistance types of advanced melanoma during anti-PD-1 monotherapy: an independent single-blind observational study on an international cohort.抗 PD-1 单药治疗期间晚期黑色素瘤的放射动力学和 SITC 定义的耐药类型:一项针对国际队列的独立单盲观察研究。
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Granzyme family acts as a predict biomarker in cutaneous melanoma and indicates more benefit from anti-PD-1 immunotherapy.颗粒酶家族作为皮肤黑色素瘤的预测生物标志物,表明其从抗 PD-1 免疫治疗中获益更多。
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Predicting anti-PD-1 responders in malignant melanoma from the frequency of S100A9+ monocytes in the blood.从血液中 S100A9+单核细胞的频率预测恶性黑色素瘤的抗 PD-1 应答者。
J Immunother Cancer. 2021 May;9(5). doi: 10.1136/jitc-2020-002171.

引用本文的文献

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Evodiamine inhibits programmed cell death ligand 1 expression via the PI3K/AKT signaling pathway to regulate antitumor immunity in melanoma.吴茱萸碱通过PI3K/AKT信号通路抑制程序性细胞死亡配体1的表达,从而调节黑色素瘤的抗肿瘤免疫。
Sci Rep. 2025 Feb 24;15(1):6649. doi: 10.1038/s41598-025-91137-2.
2
Gal-3 blocks the binding between PD-1 and pembrolizumab.半乳糖凝集素-3可阻断程序性死亡受体-1(PD-1)与派姆单抗之间的结合。
J Immunother Cancer. 2024 Oct 2;12(10):e009952. doi: 10.1136/jitc-2024-009952.
3
Multicenter proteome-wide Mendelian randomization study identifies causal plasma proteins in melanoma and non-melanoma skin cancers.
多中心蛋白质组学全基因组孟德尔随机化研究鉴定黑色素瘤和非黑色素瘤皮肤癌中的因果性血浆蛋白。
Commun Biol. 2024 Jul 13;7(1):857. doi: 10.1038/s42003-024-06538-2.