Department of Dermatology, University Hospital of Zurich, Zurich, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Am Soc Clin Oncol Educ Book. 2022 Apr;42:1-22. doi: 10.1200/EDBK_351123.
Immune checkpoint inhibitors, particularly anti-PD-1-based immune checkpoint inhibitors, have dramatically improved outcomes for patients with advanced melanoma and are currently deemed a standard of care. Ipilimumab/nivolumab is the first combination of immune checkpoint inhibitors to improve progression-free survival and overall survival in the first-line setting, with durable responses and the longest median overall survival, 72.1 months, of any drug therapy approved for advanced melanoma. However, its use is limited by the high rate of severe (grade 3-4) treatment-related adverse events. More recently, the novel immune checkpoint inhibitor combination of nivolumab/relatlimab (anti-PD-1/anti-LAG3) showed improved progression-free survival compared with nivolumab alone in the first-line setting and was well tolerated; thus, it is likely this combination will be added to the armamentarium as a first-line treatment for advanced melanoma. These changes in the treatment landscape have several treatment implications for decision-making. The choice of first-line systemic drug therapy, and the decision between immune checkpoint inhibitor monotherapy or combination therapy, requires a comprehensive assessment of disease-related factors and patient characteristics. Despite this striking progress, many patients' disease still progresses. Several new agents and therapeutic approaches are under investigation in clinical trials. Intralesional treatments hold promise for accessible metastases, although their broad application in the clinic will be limited. Prognostic and predictive biomarkers, as well as strategies to reduce treatment-related toxicities and overcome resistance, are required and are now the focus of clinical and translational research.
免疫检查点抑制剂,特别是抗 PD-1 免疫检查点抑制剂,显著改善了晚期黑色素瘤患者的预后,目前被视为标准治疗方法。Ipilimumab/nivolumab 是第一种改善一线治疗无进展生存期和总生存期的免疫检查点抑制剂联合用药,具有持久的反应和最长的中位总生存期 72.1 个月,是批准用于晚期黑色素瘤的任何药物治疗中最长的。然而,其应用受到严重(3-4 级)治疗相关不良事件发生率高的限制。最近,新型免疫检查点抑制剂 nivolumab/relatlimab(抗 PD-1/抗 LAG3)联合用药在一线治疗中与 nivolumab 单药相比,无进展生存期得到改善,且耐受性良好;因此,这种联合用药很可能会被添加到治疗晚期黑色素瘤的一线治疗方案中。这些治疗领域的变化对决策有几个治疗方面的影响。一线全身药物治疗的选择,以及免疫检查点抑制剂单药治疗还是联合治疗的决策,需要全面评估疾病相关因素和患者特征。尽管取得了这一显著进展,但许多患者的疾病仍在进展。几种新的药物和治疗方法正在临床试验中进行研究。瘤内治疗为可触及的转移灶提供了希望,尽管其在临床上的广泛应用将受到限制。需要预测和预后生物标志物以及降低治疗相关毒性和克服耐药性的策略,目前它们是临床和转化研究的重点。