免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotherapy in Melanoma.
Immunotherapy in Melanoma.
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本章探讨皮肤黑色素瘤在新辅助、辅助和 IV 期情境下的全身治疗策略。新辅助治疗旨在术前缩小肿瘤负荷,主要采用 nivolumab 联合 ipilimumab 等免疫检查点抑制剂,显示出有前景的缓解率。术后辅助治疗采用免疫疗法(如 nivolumab)和靶向治疗(如 dabrafenib 联合 trametinib),以预防高危患者复发并改善无复发生存。IV 期全身治疗针对转移性疾病,使用免疫疗法(nivolumab、pembrolizumab)和靶向丝裂原活化蛋白激酶(MAPK)通路抑制剂;BRAF 突变病例可用 dabrafenib 联合 trametinib,BRAF 野生型患者则可从 nivolumab-relatlimab 或联合治疗中获益。表格总结了关键方案、疗效和毒性。内容与临床指南一致,并更新了TIL(肿瘤浸润淋巴细胞)等新兴疗法。这些治疗根据突变状态和疾病分期进行个体化,有助于提高生存并延长无需治疗时间。
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.
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