Weill Cornell Medicine, New York, New York, USA
Department of Surgery Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
J Immunother Cancer. 2023 Oct;11(10). doi: 10.1136/jitc-2023-006947.
Since the first approval for immune checkpoint inhibitors (ICIs) for the treatment of cutaneous melanoma more than a decade ago, immunotherapy has completely transformed the treatment landscape of this chemotherapy-resistant disease. Combination regimens including ICIs directed against programmed cell death protein 1 (PD-1) with anti-cytotoxic T lymphocyte antigen-4 (CTLA-4) agents or, more recently, anti-lymphocyte-activation gene 3 (LAG-3) agents, have gained regulatory approvals for the treatment of metastatic cutaneous melanoma, with long-term follow-up data suggesting the possibility of cure for some patients with advanced disease. In the resectable setting, adjuvant ICIs prolong recurrence-free survival, and neoadjuvant strategies are an active area of investigation. Other immunotherapy strategies, such as oncolytic virotherapy for injectable cutaneous melanoma and bispecific T-cell engager therapy for HLA-A*02:01 genotype-positive uveal melanoma, are also available to patients. Despite the remarkable efficacy of these regimens for many patients with cutaneous melanoma, traditional immunotherapy biomarkers (ie, programmed death-ligand 1 expression, tumor mutational burden, T-cell infiltrate and/or microsatellite stability) have failed to reliably predict response. Furthermore, ICIs are associated with unique toxicity profiles, particularly for the highly active combination of anti-PD-1 plus anti-CTLA-4 agents. The Society for Immunotherapy of Cancer (SITC) convened a panel of experts to develop this clinical practice guideline on immunotherapy for the treatment of melanoma, including rare subtypes of the disease (eg, uveal, mucosal), with the goal of improving patient care by providing guidance to the oncology community. Drawing from published data and clinical experience, the Expert Panel developed evidence- and consensus-based recommendations for healthcare professionals using immunotherapy to treat melanoma, with topics including therapy selection in the advanced and perioperative settings, intratumoral immunotherapy, when to use immunotherapy for patients with V600-mutated disease, management of patients with brain metastases, evaluation of treatment response, special patient populations, patient education, quality of life, and survivorship, among others.
自十多年前首次批准免疫检查点抑制剂 (ICI) 治疗皮肤黑色素瘤以来,免疫疗法已彻底改变了这种对化疗耐药的疾病的治疗格局。包括针对程序性细胞死亡蛋白 1 (PD-1) 的 ICI 与抗细胞毒性 T 淋巴细胞抗原 4 (CTLA-4) 药物联合治疗,或最近与抗淋巴细胞激活基因 3 (LAG-3) 药物联合治疗的方案,已获得治疗转移性皮肤黑色素瘤的监管批准,长期随访数据表明一些晚期疾病患者有可能治愈。在可切除的情况下,辅助 ICI 延长无复发生存期,新辅助策略是一个活跃的研究领域。其他免疫疗法策略,如针对可注射皮肤黑色素瘤的溶瘤病毒治疗和针对 HLA-A*02:01 基因型阳性葡萄膜黑色素瘤的双特异性 T 细胞衔接器治疗,也可用于患者。尽管这些方案对许多皮肤黑色素瘤患者具有显著疗效,但传统的免疫疗法生物标志物(即程序性死亡配体 1 表达、肿瘤突变负担、T 细胞浸润和/或微卫星不稳定性)未能可靠地预测反应。此外,ICI 与独特的毒性特征相关,特别是针对高度活跃的抗 PD-1 联合抗 CTLA-4 药物联合治疗。免疫治疗癌症学会 (SITC) 召集了一组专家制定了这项关于免疫疗法治疗黑色素瘤的临床实践指南,包括疾病的罕见亚型(例如葡萄膜、黏膜),旨在通过为肿瘤学社区提供指导来改善患者护理。专家组从已发表的数据和临床经验中为使用免疫疗法治疗黑色素瘤的医疗保健专业人员制定了基于证据和共识的建议,涵盖了晚期和围手术期治疗选择、肿瘤内免疫治疗、何时为 V600 突变疾病患者使用免疫疗法、脑转移患者的管理、治疗反应评估、特殊患者人群、患者教育、生活质量和生存等主题。