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首页|期刊导航|中国癌症杂志|免疫检查点抑制剂在肢端型黑色素瘤治疗中的研究进展

免疫检查点抑制剂在肢端型黑色素瘤治疗中的研究进展

钱佳佳 阮聪 刘继勇 徐蕊

中国癌症杂志2025,Vol.35Issue(7):702-709,8.
中国癌症杂志2025,Vol.35Issue(7):702-709,8.DOI:10.19401/j.cnki.1007-3639.2025.07.009

免疫检查点抑制剂在肢端型黑色素瘤治疗中的研究进展

Research progress of immune checkpoint inhibitors in the treatment of acral melanoma

钱佳佳 1阮聪 1刘继勇 2徐蕊1

作者信息

  • 1. 复旦大学附属肿瘤医院闵行院区药剂科,上海 200240
  • 2. 复旦大学附属肿瘤医院闵行院区药剂科,上海 200240||复旦大学附属肿瘤医院药剂科,复旦大学上海医学院肿瘤学系,上海 200032
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摘要

Abstract

In recent years,immune checkpoint inhibitor(ICI)has led to substantial advances in the treatment of recurrent or metastatic advanced cutaneous melanoma(CM),significantly prolonging overall survival.However,due to the biological heterogeneity across melanoma subtypes,the degree of immune responsiveness varies considerably.In particular,acral melanoma(AM)(the predominant melanoma subtype in Asian populations,including China)has demonstrated limited benefit from ICI therapy,especially in the context of monotherapy.Currently,no systematic staging and standardized treatment guidelines are available for AM,and clinical evidence supporting the use of ICI in this rare subtype remains insufficient.In the neoadjuvant setting,several large phase Ⅱ/Ⅲ international trials in CM,including SWOG 1801 and NADINA,have shown that ICI-based neoadjuvant combination therapy significantly improves pathological response rates compared with traditional adjuvant approaches.Nevertheless,neoadjuvant treatment in AM remains in the exploratory stage.Early-phase clinical studies in resectable stage Ⅲ/Ⅳ AM suggest that toripalimab combined with intratumoral oncolytic virus therapy,or camrelizumab in combination with apatinib and temozolomide,may offer clinical benefit;however,confirmation of long-term survival benefit requires further validation in larger,prospective cohorts.In the adjuvant setting,for AM patients with BRAF mutations,real-world data from China have shown no significant difference in survival outcomes between dabrafenib plus trametinib and programmed death-1(PD-1)inhibitor monotherapy in high-risk resectable stage Ⅲ/Ⅳ disease,although direct head-to-head comparisons are lacking.For patients with resectable stage Ⅲ/Ⅳ wild-type AM,combination adjuvant regimens incorporating PD-1 inhibitors may provide superior recurrence risk reduction and survival benefit compared to monotherapy.In the advanced disease setting,in Chinese populations,the objective response rates of PD-1 inhibitors such as pembrolizumab,toripalimab and penpulimab remain suboptimal in AM.ICI-based combination strategies(including those with chemotherapy,anti-angiogenic agents,dual or triple immune checkpoint blockade)may improve the immune microenvironment and clinical prognosis,but concerns regarding safety and tolerability persist.For patients with ICI-refractory AM,various novel approaches combining immunotherapy,targeted agents and chemotherapy are under investigation.Additionally,several next-generation immunotherapeutic modalities[including T-cell receptor-engineered(TCR-T)therapies,therapeutic cancer vaccines,chimeric antigen receptor T(CAR-T)cell therapy and antibody-drug conjugate(ADC)]are currently in development.This review aimed to provide a comprehensive overview of current clinical evidence on the use of ICI in acral melanoma across the neoadjuvant,adjuvant,and advanced disease settings.We highlighted the efficacy and safety of existing strategies,exploreed emerging combination regimens and predictive biomarkers,and discussed key areas for future research to inform clinical decision-making and optimize outcomes in this challenging melanoma subtype.

关键词

肢端型黑色素瘤/免疫检查点抑制剂/新辅助治疗/辅助治疗/联合治疗

Key words

Acral melanoma/Immune checkpoint inhibitor/Neoadjuvant/Adjuvant/Combination therapy

分类

医药卫生

引用本文复制引用

钱佳佳,阮聪,刘继勇,徐蕊..免疫检查点抑制剂在肢端型黑色素瘤治疗中的研究进展[J].中国癌症杂志,2025,35(7):702-709,8.

基金项目

上海市闵行区卫生健康系统优秀青年药学人才计划(mwyjyx03) (mwyjyx03)

上海市闵行区自然科学研究(2023MHZ096). Excellent Young Pharmacy Talent Program of Minhang District Health System,Shanghai(mwyjyx03) (2023MHZ096)

Natural Science Research of Minhang District,Shanghai(2023MHZ096). (2023MHZ096)

中国癌症杂志

OA北大核心

1007-3639

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