Lian Bin, Guo Jun
Department of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Peking University Cancer Hospital & Institute, Beijing, China.
Am Soc Clin Oncol Educ Book. 2025 Jun;45(3):e4733858. doi: 10.1200/EDBK-25-473858. Epub 2025 May 28.
Mucosal melanoma (MM) is a rare and aggressive subtype of melanoma arising from mucosal tissues, with distinct genomic and clinical characteristics compared with cutaneous melanoma (CM). Despite therapeutic advancements, MM remains challenging to treat because of late diagnosis, high heterogeneity, and limited efficacy of conventional therapies. This review synthesizes current knowledge on the genomic landscape of MM and explores the tumor microenvironment that influences treatment resistance. Emerging therapeutic approaches, including neoadjuvant and adjuvant therapies, are critically evaluated. Targeted therapy (eg, BRAF/MEK and KIT inhibitors) demonstrated comparable efficacy in advanced MM and CM. Although immune checkpoint inhibitors show promise in CM, their efficacy in MM is modest, with antiangiogenic-based combination therapies offering potential improvements. Preclinical and ongoing clinical trials underscore the need for personalized treatment strategies on the basis of molecular profiling. This review emphasizes the urgency for further research to address the unmet needs in MM management and improve patient outcomes.
黏膜黑色素瘤(MM)是一种源自黏膜组织的罕见且侵袭性黑色素瘤亚型,与皮肤黑色素瘤(CM)相比具有独特的基因组和临床特征。尽管治疗取得了进展,但由于诊断较晚、高度异质性以及传统疗法疗效有限,MM的治疗仍然具有挑战性。本综述综合了关于MM基因组格局的当前知识,并探讨了影响治疗耐药性的肿瘤微环境。对包括新辅助和辅助治疗在内的新兴治疗方法进行了批判性评估。靶向治疗(如BRAF/MEK和KIT抑制剂)在晚期MM和CM中显示出相当的疗效。尽管免疫检查点抑制剂在CM中显示出前景,但其在MM中的疗效一般,基于抗血管生成的联合疗法可能会有所改善。临床前和正在进行的临床试验强调了基于分子谱分析制定个性化治疗策略的必要性。本综述强调了进一步研究以满足MM管理中未满足需求并改善患者预后的紧迫性。