New Standards in the Treatment of Advanced Metastatic Melanoma: Immunotherapy and BRAF-Targeted Therapies as Emerging Paradigms.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Firas Kreidieh, Michael K Wong
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引用次数: 0

Abstract

Although cutaneous melanoma accounts for only about 2% of skin cancers, its rapid progression makes it an aggressive skin cancer with a high mortality rate. As of 2018, the SEER database estimated that the 5-year overall survival (OS) rate is 29.8% in patients with stage IV disease at diagnosis in the United States. Non-cutaneous melanoma, including mucosal and uveal subtypes, carries a generally worse prognosis. Once considered refractory to conventional treatments, such as chemotherapy and radiation therapy, the advent of immunotherapy, including immune checkpoint inhibitors (ICIs), vaccines, and tumor-infiltrating lymphocytes (TIL), and of targeted therapy over the past decade has resulted in dramatic improvements in melanoma. Importantly, ICIs have resulted in long-term remission for patients with melanoma, thus introducing the possibility of a cure for some patients with metastatic disease. These include antibodies against programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1), cytotoxic T-lymphocyte antigen-4 (CTLA-4), and lymphocyte activation gene-3 (LAG-3). In this review, we will provide an overview of metastatic melanoma while focusing on its current pharmacologic armamentarium, toxicities of treatment, including ICIs and targeted therapy, and its therapeutic clinical strategies. The therapeutic advances presented in this review serve as the foundation for an ever-expanding repertoire of innovative approaches. These include mRNA vaccines, oncolytic viruses, bispecific engagers, oral immunomodulators, and novel cytokines. Adoptive cellular strategies are evolving to TILS transduced with conditional gene expression cassettes, as well as non-T cell approaches involving dendritic cells and natural killer (NK) cells. Targeted therapy strategies have broadened to include upstream components of RAS, other MAP kinase pathways, and HDAC inhibitors, among others. All these new paradigms translate into increasingly complex decision-making for the treatment team, a burden that is more than offset by the tremendous benefit for melanoma patients. This is truly the beginning of a new era.

晚期转移性黑色素瘤治疗的新标准:免疫治疗和braf靶向治疗作为新兴范例。
虽然皮肤黑色素瘤只占皮肤癌的2%左右,但它的快速进展使其成为一种具有高死亡率的侵袭性皮肤癌。截至2018年,SEER数据库估计,在美国诊断为IV期疾病的患者,5年总生存率(OS)为29.8%。非皮肤黑色素瘤,包括粘膜和葡萄膜亚型,通常预后较差。在过去的十年里,免疫疗法的出现,包括免疫检查点抑制剂(ICIs)、疫苗和肿瘤浸润淋巴细胞(TIL),以及靶向治疗,曾被认为对化疗和放疗等常规治疗难以治愈,导致了黑色素瘤的显著改善。重要的是,ICIs已经导致黑色素瘤患者的长期缓解,从而为一些转移性疾病患者带来治愈的可能性。这些抗体包括抗程序性细胞死亡-1 (PD-1)/程序性细胞死亡配体-1 (PD-L1)、细胞毒性t淋巴细胞抗原-4 (CTLA-4)和淋巴细胞活化基因-3 (LAG-3)的抗体。在这篇综述中,我们将提供转移性黑色素瘤的概述,同时重点介绍其目前的药理学,治疗的毒性,包括ICIs和靶向治疗,以及其治疗的临床策略。本综述中提出的治疗进展为不断扩展的创新方法奠定了基础。这些包括mRNA疫苗、溶瘤病毒、双特异性接合物、口服免疫调节剂和新型细胞因子。过继细胞策略正在演变为由条件基因表达磁带转导的TILS,以及涉及树突状细胞和自然杀伤(NK)细胞的非t细胞方法。靶向治疗策略已经扩大到包括RAS的上游成分、其他MAP激酶途径和HDAC抑制剂等。所有这些新的范例转化为治疗团队越来越复杂的决策,这一负担被黑色素瘤患者的巨大利益所抵消。这确实是一个新时代的开始。
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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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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