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

机译:针对治疗转移性黑色素瘤的免疫疗法组合的靶向疗法

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摘要

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 controlwhen targeted and immune checkpoint agents are combined. Therefore, combination strategies with targeted and immune checkpoint therapy may improve patient outcomes. Early clinical data with antiprogrammed 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.
机译:近年来,肿瘤学领域目睹了治疗晚期恶性肿瘤的许多突破,特别是在先进的黑素瘤患者中。有针对性的和免疫检查点疗法被出现为这些患者的主要治疗策略。黑色素瘤的分子分析掺入常规实践中以鉴定潜在的治疗靶标,患者提供靶向或免疫检查点抑制剂治疗方法。两种策略都有局限性,并非所有患者都经历持久的反应。临床前数据证明了靶向治疗能力,增强效应T细胞的活性,减少免疫抑制细胞因子产生,并增加肿瘤细胞抗原呈递,这可能增加抗肿瘤免疫力。在体内模型中表明,随着靶向和免疫检查点的改善,组合了改善的肿瘤控制。因此,具有针对性和免疫检查点治疗的组合策略可能会改善患者的结果。具有抗抗型细胞死亡蛋白的早期临床数据/编程的细胞死亡配体1剂与靶向抑制剂组合的药剂似乎具有可接受的毒性率和增强抗肿瘤活性的可能性。本综述探讨了先进黑素瘤患者这些联合方法的临床前和临床开发现状。

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