研究概要
尽管皮肤黑色素瘤仅占皮肤癌的约 2%,但其快速进展使其成为一种高死亡率的侵袭性皮肤癌。
中文摘要
尽管皮肤黑色素瘤约占皮肤癌的2%,但其进展迅速,是一种死亡率较高的侵袭性皮肤癌。根据截至2018年的SEER数据库估计,美国确诊时为IV期的患者5年总生存率为29.8%。包括黏膜和葡萄膜亚型在内的非皮肤黑色素瘤通常预后更差。过去黑色素瘤被认为对化疗和放疗等传统治疗难治;近十年来,免疫治疗(包括免疫检查点抑制剂、疫苗和TIL(肿瘤浸润淋巴细胞)〔TIL〕)以及靶向治疗的出现,显著改善了黑色素瘤的治疗效果。值得注意的是,免疫检查点抑制剂可使黑色素瘤患者获得长期缓解,因此部分转移性疾病患者有望治愈。这类药物包括靶向程序性细胞死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)、细胞毒性T淋巴细胞相关抗原4(CTLA-4)及淋巴细胞活化基因3(LAG-3)的抗体。本综述概述转移性黑色素瘤,重点介绍当前药物治疗手段、免疫检查点抑制剂和靶向治疗的毒性,以及治疗临床策略。本文介绍的治疗进展为不断扩展的创新疗法奠定基础,包括mRNA疫苗、溶瘤病毒、双特异性衔接分子、口服免疫调节剂和新型细胞因子。过继细胞策略正发展为转导条件性基因表达盒的TIL疗法,以及涉及树突状细胞和自然杀伤(NK)细胞的非T细胞疗法。靶向治疗策略也已扩展至RAS上游组分、其他丝裂原活化蛋白激酶(MAPK)通路及组蛋白去乙酰化酶(HDAC)抑制剂等。这些新模式使治疗团队面临日益复杂的决策,但由此带来的负担远不及其为黑色素瘤患者带来的巨大获益。这确实是一个新时代的开端。
展开英文摘要原文
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.
论文信息
- 作者
- Kreidieh F、Wong MK
- 第一作者单位
- Clinical Medicine- Division of Hematology-Oncology, Associate Director- Internal Medicine Residency Program, American University of Beirut, Beirut, Lebanon.
- 通讯作者单位
- Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.United States
- 文献类型
- 综述
- 期刊
- Current pharmaceutical design2026