Zenderowski Veronika, Schreieder Laura, Drexler Konstantin, Haferkamp Sebastian
Klinik und Poliklinik für Dermatologie und Venerologie, Universitätsklinikum Regensburg, Franz-Josef-Strauß-Allee 11, 93053, Regensburg, Deutschland.
Dermatologie (Heidelb). 2025 Jun;76(6):354-360. doi: 10.1007/s00105-025-05508-x. Epub 2025 May 23.
Although effective treatment options for malignant melanoma already exist, currently available adjuvant and neoadjuvant therapies are not always sufficient to prevent relapse or ensure a long-term treatment response. Many patients develop resistance or show inadequate responses to existing therapies. Therefore, there is an urgent need for new and more effective therapeutic approaches in the adjuvant and neoadjuvant settings to sustainably improve patient prognosis.
This study provides an overview of current developments in melanoma treatment, with a particular focus on the adjuvant and neoadjuvant application of novel immunotherapies.
A literature search and discussion of relevant recent studies was carried out.
Adjuvant mRNA-based adjuvant treatment combined with pembrolizumab demonstrated a significantly improved relapse-free survival compared to pembrolizumab monotherapy (79% vs. 62%). The value of adjuvant LAG‑3 antibodies in combination with PD‑1 blockers remains inconclusive. A neoadjuvant intralesional treatment with daromun after complete removal of tumor tissue reduced the risk of recurrence by 41% and led to a significant extension in relapse-free survival (16.7 months vs. 6.8 months). Tebentafusp improved overall survival in metastatic uveal melanoma and is currently being investigated in the adjuvant and neoadjuvant setting.
The mRNA-based treatment combined with checkpoint inhibitors have the potential to induce long-term immune responses. The efficacy of LAG-3 inhibitors in the adjuvant setting is currently under evaluation in clinical studies. The immunocytokine treatment with daromun shows promising results in the neoadjuvant setting by stimulating both local and systemic immune responses. Future studies should focus on identifying optimal combinations of treatment to improve the long-term prognosis of patients.
尽管恶性黑色素瘤已有有效的治疗方案,但目前可用的辅助和新辅助治疗并不总能预防复发或确保长期治疗反应。许多患者对现有疗法产生耐药性或反应不佳。因此,迫切需要在辅助和新辅助治疗中采用更新、更有效的治疗方法,以可持续地改善患者预后。
本研究概述了黑色素瘤治疗的当前进展,特别关注新型免疫疗法的辅助和新辅助应用。
进行了文献检索并讨论了近期相关研究。
与帕博利珠单抗单药治疗相比,基于mRNA的辅助治疗联合帕博利珠单抗可显著提高无复发生存率(79%对62%)。辅助性LAG-3抗体联合PD-1阻断剂的价值尚无定论。在肿瘤组织完全切除后,采用达罗木单抗进行新辅助病灶内治疗可将复发风险降低41%,并显著延长无复发生存期(16.7个月对6.8个月)。替贝福司改善了转移性葡萄膜黑色素瘤的总生存期,目前正在辅助和新辅助治疗环境中进行研究。
基于mRNA的治疗联合检查点抑制剂有潜力诱导长期免疫反应。LAG-3抑制剂在辅助治疗中的疗效目前正在临床研究中评估。达罗木单抗的免疫细胞因子治疗通过刺激局部和全身免疫反应,在新辅助治疗中显示出有前景的结果。未来的研究应专注于确定最佳治疗组合,以改善患者的长期预后。