Targeted Therapies in Combination With Immune Therapies for the Treatment of Metastatic Melanoma

S. Christiansen, Shaheer Khan, G. Gibney
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引用次数: 10

Abstract

Abstract In recent years, the field of oncology has witnessed many breakthroughs in the treatment of advanced malignancies, particularly in patients with advanced melanoma. Targeted and immune checkpoint therapies have emerged as the primary treatment strategies for these patients. Molecular profiling of melanoma is incorporated into routine practice to identify potential therapeutic targets, and patients are offered either a targeted or immune checkpoint inhibitor therapy approach. Both strategies have limitations where not all patients experience durable responses. Preclinical data have demonstrated the ability of targeted therapy to enhance activity of effector T cells, reduce immunosuppressive cytokine production, and increase tumor cell antigen presentation, which can augment antitumor immunity. In vivo models have shown synergy with improved tumor control when targeted and immune checkpoint agents are combined. Therefore, combination strategies with targeted and immune checkpoint therapy may improve patient outcomes. Early clinical data with anti–programmed cell-death protein 1/programmed cell-death ligand 1 agents in combination with targeted inhibitors appear to have acceptable toxicity rates and the potential for enhanced antitumor activity. This review explores the current status of preclinical and clinical development for these combination approaches in patients with advanced melanoma.
靶向疗法联合免疫疗法治疗转移性黑色素瘤
近年来,肿瘤学领域在晚期恶性肿瘤的治疗方面取得了许多突破,特别是在晚期黑色素瘤患者的治疗方面。靶向和免疫检查点疗法已成为这些患者的主要治疗策略。黑色素瘤的分子谱分析被纳入常规实践,以确定潜在的治疗靶点,并为患者提供靶向或免疫检查点抑制剂治疗方法。这两种策略都有局限性,因为并非所有患者都有持久的反应。临床前数据表明,靶向治疗能够增强效应T细胞的活性,减少免疫抑制性细胞因子的产生,增加肿瘤细胞抗原的呈递,从而增强抗肿瘤免疫。体内模型显示,当靶向和免疫检查点药物联合使用时,协同作用改善了肿瘤控制。因此,联合靶向治疗和免疫检查点治疗可以改善患者的预后。抗程序性细胞死亡蛋白1/程序性细胞死亡配体1药物与靶向抑制剂联合使用的早期临床数据似乎具有可接受的毒性率和增强抗肿瘤活性的潜力。这篇综述探讨了这些联合方法在晚期黑色素瘤患者的临床前和临床发展现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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