以程序性细胞死亡1/程序性细胞死亡配体1检查点抑制剂为骨干的新组合策略

S. Hu-Lieskovan, A. Ribas
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引用次数: 43

摘要

免疫检查点的发现和随后检查点抑制剂的临床开发已经彻底改变了肿瘤学领域。抗肿瘤免疫反应的持久性提高了患者长期生存和潜在治愈的希望;然而,目前只有少数患者有反应。在预测性生物标志物的指导下,联合策略有助于增加抗原释放和t细胞启动,促进t细胞活化和归巢,改善肿瘤免疫微环境,有助于克服肿瘤免疫逃避机制,最大限度地提高疗效,最终使大多数患者受益。由于复杂的潜在生物学,不可预测的毒性和准确的反应评估,巨大的挑战仍然存在。在配对活检转化研究的指导下,精心设计的临床试验将是开发可靠的预测性生物标志物的关键,以选择哪些患者最有可能从每种策略中受益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Combination Strategies Using Programmed Cell Death 1/Programmed Cell Death Ligand 1 Checkpoint Inhibitors as a Backbone
Abstract The discovery of immune checkpoints and subsequent clinical development of checkpoint inhibitors have revolutionized the field of oncology. The durability of the antitumor immune responses has raised the hope for long-term patient survival and potential cure; however, currently, only a minority of patients respond. Combination strategies to help increase antigen release and T-cell priming, promote T-cell activation and homing, and improve the tumor immune microenvironment, all guided by predictive biomarkers, can help overcome the tumor immune-evasive mechanisms and maximize efficacy to ultimately benefit the majority of patients. Great challenges remain because of the complex underlying biology, unpredictable toxicity, and accurate assessment of response. Carefully designed clinical trials guided by translational studies of paired biopsies will be key to develop reliable predictive biomarkers to choose which patients would most likely benefit from each strategy.
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