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A systematic review on the emerging association between the occurrence of immune-related adverse events and clinical outcomes with checkpoint inhibitors in advanced cancer patients

机译:对晚期癌症患者检查点抑制剂的免疫相关不良事件发生与临床结果之间的新出现关联的系统综述

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The correlation between clinical outcomes and treatment-related adverse events (AEs) has always been a debated topic in clinical oncology. Despite toxicities pharmacodynamics effects, the misunderstanding has always been around the corner: AEs themselves could lead to morbidity and mortality; on the other hand, the choice of the clinical outcomes to measure is not univocal. After the advent of immune checkpoint inhibitors (ICIs), such as anti-cytotoxic T-lymphocyte-associated protein 4 and anti-programmed death-1/programmed death ligand-1, new class-specific AEs have emerged, called immune-related AEs (irAEs). With irAEs, the correlation between toxicity and clinical outcomes has suddenly been suggested, but it is still to be proven. We conducted a systematic literature review regarding this emerging association, pointing out all the available data and speculating on the possible underlying mechanisms. Thirty-six studies were included in the analysis, involving different malignancies (mostly melanoma and lung cancer), with different measured clinical outcomes. The most of them were retrospective. Despite the high heterogeneity, and the enormous biases of the revised studies, we can assume that irAEs occurrence is linked to the therapeutic activity of immune checkpoint inhibitors, with a (certain) direct proportionality, maybe subtending the likelihood of an immunogenic phenotype. This phenomenon seems to occur with both anti-cytotoxic T-lymphocyte-associated protein 4 and anti-programmed death-1/programmed death ligand-1, and across different solid malignancies. (C) 2019 Elsevier Inc. All rights reserved.
机译:临床结果与治疗相关的不良事件(AES)之间的相关性始终是临床肿瘤学中的争论。尽管有毒的药效学效应,但误区一直在拐角处:AES自己可能导致发病率和死亡率;另一方面,选择临床结果的测量不是单一的。免疫检查点抑制剂(ICIS)的出现后,如抗细胞毒性T淋巴细胞相关蛋白4和反向死亡-1 /编程死亡配体-1,新类特定AES已经出现,称为免疫相关的AES (伊拉斯)。与伊拉斯一起,突然提出了毒性与临床结果之间的相关性,但仍然被证明。我们对该新兴协会进行了系统的文献综述,指出所有可用数据并拨出可能的潜在机制。分析中包含三十六项研究,涉及不同的恶性肿瘤(大多数黑素瘤和肺癌),具有不同的测量临床结果。他们中的大多数是回顾性的。尽管具有高异质性和修订研究的巨大偏见,但我们可以假设伊拉什发生与免疫检查点抑制剂的治疗活性有关,具有(某些)直接比例,也许与免疫原性表型的可能性进行了结束。这种现象似乎发生在抗细胞毒性T淋巴细胞相关蛋白4和反编程死亡-1 /编程死亡配体-1,以及不同的固体恶性肿瘤。 (c)2019 Elsevier Inc.保留所有权利。

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