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黑色素瘤的免疫疗法:进展、陷阱与未来展望。

Immunotherapy in melanoma: advances, pitfalls, and future perspectives.

作者信息

Sorino Cristina, Iezzi Simona, Ciuffreda Ludovica, Falcone Italia

机构信息

SAFU, Department of Research, Advanced Diagnostics, and Technological Innovation, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.

出版信息

Front Mol Biosci. 2024 Jun 28;11:1403021. doi: 10.3389/fmolb.2024.1403021. eCollection 2024.

DOI:10.3389/fmolb.2024.1403021
PMID:39086722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11289331/
Abstract

Cutaneous melanoma is the deadliest and most aggressive form of skin cancer owing to its high capacity for metastasis. Over the past few decades, the management of this type of malignancy has undergone a significant revolution with the advent of both targeted therapies and immunotherapy, which have greatly improved patient quality of life and survival. Nevertheless, the response rates are still unsatisfactory for the presence of side effects and development of resistance mechanisms. In this context, tumor microenvironment has emerged as a factor affecting the responsiveness and efficacy of immunotherapy, and the study of its interplay with the immune system has offered new promising clinical strategies. This review provides a brief overview of the currently available immunotherapeutic strategies for melanoma treatment by analyzing both the positive aspects and those that require further improvement. Indeed, a better understanding of the mechanisms involved in the immune evasion of melanoma cells, with particular attention on the role of the tumor microenvironment, could provide the basis for improving current therapies and identifying new predictive biomarkers.

摘要

皮肤黑色素瘤是最致命、侵袭性最强的皮肤癌形式,因其具有高转移能力。在过去几十年里,随着靶向治疗和免疫治疗的出现,这种恶性肿瘤的治疗发生了重大变革,极大地改善了患者的生活质量和生存率。然而,由于副作用的存在和耐药机制的产生,反应率仍不尽人意。在此背景下,肿瘤微环境已成为影响免疫治疗反应性和疗效的一个因素,对其与免疫系统相互作用的研究提供了新的有前景的临床策略。本综述通过分析当前可用的黑色素瘤免疫治疗策略的积极方面和需要进一步改进的方面,对其进行简要概述。事实上,更好地理解黑色素瘤细胞免疫逃逸所涉及的机制,尤其关注肿瘤微环境的作用,可为改进当前治疗方法和识别新的预测生物标志物提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbb/11289331/60f9254197d9/fmolb-11-1403021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbb/11289331/c5bd11d038c4/fmolb-11-1403021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbb/11289331/60f9254197d9/fmolb-11-1403021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbb/11289331/c5bd11d038c4/fmolb-11-1403021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbb/11289331/60f9254197d9/fmolb-11-1403021-g002.jpg

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本文引用的文献

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Individualised neoantigen therapy mRNA-4157 (V940) plus pembrolizumab versus pembrolizumab monotherapy in resected melanoma (KEYNOTE-942): a randomised, phase 2b study.个体化新抗原疗法mRNA-4157(V940)联合帕博利珠单抗与帕博利珠单抗单药治疗可切除黑色素瘤(KEYNOTE-942):一项随机2b期研究
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The role of triple therapy and therapy sequence in treatment of BRAF-mutant metastatic melanoma. Response to overall survival with first-line atezolizumab in combination with vemurafenib and cobimetinib in BRAFV600 mutation-positive advanced melanoma (IMspire150): second interim analysis of a multicentre, randomised, phase 3 study.
皮肤黑色素瘤中基质金属蛋白酶的综合研究:诊断、预后及治疗见解
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BRAF 突变型转移性黑色素瘤的三联疗法和治疗顺序的作用。在 BRAFV600 突变阳性的晚期黑色素瘤(IMspire150)患者中,一线阿特珠单抗联合维莫非尼和考比替尼的总生存期:多中心、随机、3 期研究的第二次期中分析。
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