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Mass Spectrometry-Based Multivariate Proteomic Tests for Prediction of Outcomes on Immune Checkpoint Blockade Therapy: The Modern Analytical Approach

机译:基于质谱的多元蛋白质组学测试用于免疫检查点封锁疗法的结果预测:现代分析方法

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摘要

The remarkable success of immune checkpoint inhibitors (ICIs) has given hope of cure for some patients with advanced cancer; however, the fraction of responding patients is 15–35%, depending on tumor type, and the proportion of durable responses is even smaller. Identification of biomarkers with strong predictive potential remains a priority. Until now most of the efforts were focused on biomarkers associated with the assumed mechanism of action of ICIs, such as levels of expression of programmed death-ligand 1 (PD-L1) and mutation load in tumor tissue, as a proxy of immunogenicity; however, their performance is unsatisfactory. Several assays designed to capture the complexity of the disease by measuring the immune response in tumor microenvironment show promise but still need validation in independent studies. The circulating proteome contains an additional layer of information characterizing tumor–host interactions that can be integrated into multivariate tests using modern machine learning techniques. Here we describe several validated serum-based proteomic tests and their utility in the context of ICIs. We discuss test performances, demonstrate their independence from currently used biomarkers, and discuss various aspects of associated biological mechanisms. We propose that serum-based multivariate proteomic tests add a missing piece to the puzzle of predicting benefit from ICIs.
机译:免疫检查点抑制剂(ICIs)的巨大成功为治愈某些晚期癌症患者带来了希望。然而,根据肿瘤类型的不同,有反应的患者比例为15%至35%,而持久反应的比例甚至更低。鉴定具有强预测潜力的生物标志物仍然是优先事项。迄今为止,大多数努力都集中在与假定的ICI作用机制相关的生物标记物上,例如程序性死亡配体1(PD-L1)的表达水平和肿瘤组织中的突变负荷,作为免疫原性的代理。但是,它们的性能不能令人满意。旨在通过测量肿瘤微环境中的免疫反应来捕获疾病复杂性的几种检测方法显示出了希望,但仍需要在独立研究中进行验证。循环蛋白质组包含表征肿瘤-宿主相互作用的另一层信息,可以使用现代机器学习技术将其集成到多变量测试中。在这里,我们描述了几种经过验证的基于血清的蛋白质组学测试及其在ICIs中的效用。我们讨论测试性能,证明其与当前使用的生物标志物的独立性,并讨论相关生物学机制的各个方面。我们建议基于血清的多元蛋白质组学测试为预测ICI带来的益处增加了一个缺失。

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