Exploring resistance to immune checkpoint inhibitors and targeted therapies in melanoma.

IF 4.6 Q1 ONCOLOGY
癌症耐药(英文) Pub Date : 2024-10-31 eCollection Date: 2024-01-01 DOI:10.20517/cdr.2024.54
Anum Jalil, Melissa M Donate, Jane Mattei
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引用次数: 0

Abstract

Melanoma is the most aggressive form of skin cancer, characterized by a poor prognosis, and its incidence has risen rapidly over the past 30 years. Recent therapies, notably immunotherapy and targeted therapy, have significantly improved the outcome of patients with metastatic melanoma. Previously dismal five-year survival rates of below 5% have shifted to over 50% of patients surviving the five-year mark, marking a significant shift in the landscape of melanoma treatment and survival. Unfortunately, about 50% of patients either do not respond to therapy or experience early or late relapses following an initial response. The underlying mechanisms for primary and secondary resistance to targeted therapies or immunotherapy and relapse patterns remain not fully identified. However, several molecular pathways and genetic factors have been associated with melanoma resistance to these treatments. Understanding these mechanisms paves the way for creating novel treatments that can address resistance and ultimately enhance patient outcomes in melanoma. This review explores the mechanisms behind immunotherapy and targeted therapy resistance in melanoma patients. Additionally, it describes the treatment strategies to overcome resistance, which have improved patients' outcomes in clinical trials and practice.

探索黑色素瘤对免疫检查点抑制剂和靶向疗法的耐药性。
黑色素瘤是最具侵袭性的皮肤癌,其特点是预后不良,在过去 30 年中发病率迅速上升。最近的疗法,尤其是免疫疗法和靶向疗法,大大改善了转移性黑色素瘤患者的预后。患者的五年生存率从以前的不足 5%,到现在的超过 50%,标志着黑色素瘤治疗和生存状况的重大转变。遗憾的是,约 50%的患者要么对治疗无反应,要么在初次反应后出现早期或晚期复发。靶向疗法或免疫疗法的原发性和继发性耐药性以及复发模式的基本机制仍未完全确定。不过,有几种分子途径和遗传因素与黑色素瘤对这些疗法的耐药性有关。了解这些机制可为创造新型治疗方法铺平道路,从而解决耐药性问题,并最终改善黑色素瘤患者的预后。本综述探讨了黑色素瘤患者对免疫疗法和靶向疗法产生耐药性的机制。此外,它还介绍了克服耐药性的治疗策略,这些策略在临床试验和实践中改善了患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.60
自引率
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