Prkačin Ivana, Brkić Ana, Pondeljak Nives, Mokos Mislav, Gaćina Klara, Šitum Mirna
Department of Dermatology and Venereology, Sestre Milosrdnice University Hospital Center, 10000 Zagreb, Croatia.
Department for Human Sciences, School of Medicine, University of Split, 21000 Split, Croatia.
Biomedicines. 2025 Aug 4;13(8):1894. doi: 10.3390/biomedicines13081894.
: Patients with resected stage IIB and IIC melanoma are at high risk of recurrence and distant metastasis, despite surgical treatment. The recent emergence of immune checkpoint inhibitors (ICIs) has led to their evaluation in the adjuvant setting for early-stage disease. This review aims to synthesize current evidence regarding adjuvant immunotherapy for stage IIB/IIC melanoma, explore emerging strategies, and highlight key challenges and future directions. : We conducted a comprehensive literature review of randomized clinical trials, observational studies, and relevant mechanistic and biomarker research on adjuvant therapy in stage IIB/IIC melanoma. Particular focus was placed on pivotal trials evaluating PD-1 inhibitors (KEYNOTE-716 and CheckMate 76K), novel vaccine and targeted therapy trials, mechanisms of resistance, immune-related toxicity, and biomarker development. : KEYNOTE-716 and CheckMate 76K demonstrated significant improvements in recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) with pembrolizumab and nivolumab, respectively, compared to placebo. However, no definitive overall survival benefit has yet been shown. Adjuvant immunotherapy is linked to immune-related adverse events, including permanent endocrinopathies. Emerging personalized approaches, such as circulating tumor DNA monitoring and gene expression profiling, may enhance patient selection, but remain investigational. : Adjuvant PD-1 blockade offers clear RFS benefits in high-risk stage II melanoma, but optimal patient selection remains challenging, due to uncertain overall survival benefit and toxicity concerns. Future trials should integrate biomarker-driven approaches to refine therapeutic decisions and minimize overtreatment.
尽管接受了手术治疗,但IIB期和IIC期黑色素瘤切除患者仍有较高的复发和远处转移风险。免疫检查点抑制剂(ICI)的近期出现促使其在早期疾病辅助治疗中的评估。本综述旨在综合目前关于IIB/IIC期黑色素瘤辅助免疫治疗的证据,探索新出现的策略,并突出关键挑战和未来方向。我们对IIB/IIC期黑色素瘤辅助治疗的随机临床试验、观察性研究以及相关机制和生物标志物研究进行了全面的文献综述。特别关注评估PD-1抑制剂的关键试验(KEYNOTE-716和CheckMate 76K)、新型疫苗和靶向治疗试验、耐药机制、免疫相关毒性以及生物标志物开发。KEYNOTE-716和CheckMate 76K分别显示,与安慰剂相比,帕博利珠单抗和纳武利尤单抗在无复发生存期(RFS)和无远处转移生存期(DMFS)方面有显著改善。然而,尚未显示出明确的总生存获益。辅助免疫治疗与免疫相关不良事件有关,包括永久性内分泌病变。新出现的个性化方法,如循环肿瘤DNA监测和基因表达谱分析,可能会改善患者选择,但仍处于研究阶段。辅助性PD-1阻断在高危II期黑色素瘤中提供了明确的RFS益处,但由于总生存获益不确定和毒性问题,最佳患者选择仍然具有挑战性。未来的试验应整合生物标志物驱动的方法,以完善治疗决策并尽量减少过度治疗。