The Christie NHS Foundation Trust, Department of Medical Oncology, Manchester, UK; The University of Manchester, Division of Cancer Sciences, Manchester, UK.
University of Perugia, Perugia, Italy; Ospedale Papa Givoanni XXIII, Bergamo, Italy.
Eur J Cancer. 2023 Aug;189:112914. doi: 10.1016/j.ejca.2023.05.003. Epub 2023 May 8.
Immunotherapy with checkpoint inhibitors has revolutionised the outcomes for melanoma patients. In the metastatic setting, patients treated with nivolumab and ipilimumab have an expected 5-year survival of> 50%. For patients with resected high-risk stage III disease, adjuvant pembrolizumab, nivolumab or dabrafenib and trametinib are associated with a significant improvement in both relapse-free survival (RFS) and distant metastasis-free survival (DMFS). More recently neoadjuvant immunotherapy has shown very promising outcomes in patients with clinically detectable nodal disease and is likely to become a new standard of care. For stage IIB/C disease, two pivotal adjuvant trials of pembrolizumab and nivolumab have also reported a significant improvement in both RFS and DMFS. However, the absolute benefit is low and there are concerns about the risk of severe toxicities as well as long-term morbidity from endocrine toxicity. Ongoing registration phase III trials are currently evaluating newer immunotherapy combinations and the role of BRAF/MEK-directed targeted therapy for stage II melanoma. However, our ability to personalise therapy based on molecular risk stratification has lagged behind the development of novel immune therapies. There is a critical need to evaluate the use of tissue and blood-based biomarkers, to better select patients that will recur and avoid unnecessary treatment for the majority of patients cured by surgery alone.
免疫疗法与检查点抑制剂已彻底改变了黑色素瘤患者的预后。在转移性疾病的治疗中,接受纳武单抗和伊匹单抗治疗的患者 5 年预期生存率>50%。对于接受切除的高风险 III 期疾病的患者,辅助帕博利珠单抗、纳武单抗或达拉非尼联合曲美替尼治疗与无复发生存(RFS)和远处无转移生存(DMFS)的显著改善相关。最近,新辅助免疫疗法在具有临床可检测的淋巴结疾病的患者中显示出非常有希望的结果,可能成为一种新的治疗标准。对于 IIB/C 期疾病,帕博利珠单抗和纳武单抗的两项关键性辅助试验也报告了 RFS 和 DMFS 的显著改善。然而,绝对获益较低,并且人们对严重毒性以及内分泌毒性的长期发病率的风险存在担忧。目前正在进行的 III 期注册试验正在评估新型免疫疗法组合以及针对 II 期黑色素瘤的 BRAF/MEK 靶向治疗的作用。然而,我们基于分子风险分层来个性化治疗的能力落后于新型免疫疗法的发展。迫切需要评估组织和基于血液的生物标志物的使用,以更好地选择可能复发的患者,并避免对大多数通过手术治愈的患者进行不必要的治疗。