Immunotherapy in Melanoma.

Q2 Medicine
Yan Xing, Helena T Wu, Swapnil Rajurkar, Tingting Tan, Vanessa Hsu
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引用次数: 0

Abstract

This chapter explores systemic treatment strategies for cutaneous melanoma across neoadjuvant, adjuvant, and Stage IV settings. Neoadjuvant therapy aims to reduce tumor burden pre-surgery, primarily using immune checkpoint inhibitors like nivolumab plus ipilimumab, showing promising response rates. Adjuvant therapy, post-resection, leverages immunotherapy (e.g., nivolumab) and targeted therapies (e.g., dabrafenib plus trametinib) to prevent recurrence in high-risk patients, improving relapse-free survival. Stage IV systemic treatment addresses metastatic disease, employing immunotherapy (nivolumab, pembrolizumab) and targeted mitogen-activated protein kinase (MAPK) pathway inhibitors (dabrafenib plus trametinib) for BRAF-mutant cases, while BRAF wild-type patients benefit from nivolumab-relatlimab or combination therapies. Tables summarize key regimens, efficacy, and toxicities. Content aligns with clinical guidelines, with updates on emerging therapies like tumor-infiltrating lymphocytes (TIL). These approaches enhance survival and treatment-free intervals, tailored to mutation status and disease stage.

黑色素瘤的免疫治疗。
本章探讨了皮肤黑色素瘤的新辅助、辅助和IV期治疗策略。新辅助治疗的目的是在手术前减少肿瘤负担,主要使用免疫检查点抑制剂,如nivolumab和ipilimumab,显示出有希望的反应率。术后辅助治疗利用免疫治疗(如纳武单抗)和靶向治疗(如达拉法尼加曲美替尼)预防高危患者复发,提高无复发生存率。IV期全身治疗针对转移性疾病,针对BRAF突变病例采用免疫治疗(nivolumab, pembrolizumab)和靶向丝裂原活化蛋白激酶(MAPK)途径抑制剂(dabrafenib + trametinib),而BRAF野生型患者则受益于nivolumab- relatlimumab或联合治疗。表格总结了主要的治疗方案、疗效和毒性。内容与临床指南保持一致,并更新了肿瘤浸润淋巴细胞(TIL)等新兴疗法。这些方法可根据突变状态和疾病阶段提高生存率和无治疗间隔。
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
Cancer treatment and research
Cancer treatment and research Medicine-Oncology
CiteScore
1.00
自引率
0.00%
发文量
11
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