Blood-based circulating biomarkers for prediction of immune-checkpoint inhibitors efficacy in renal cell carcinoma.

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-09-20 DOI:10.37349/etat.2024.00271
Loubna Omri, Marie Naigeon, Ronan Flippot, Javier Gavira-Díaz, Jesus Poveda-Ferriols, Dan Nguyen, Chaimae Abdi, Alvaro Arroyo-Salgado, Nathalie Chaput, Guillermo de Velasco, Laurence Albigès, Lucía Carril-Ajuria
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引用次数: 0

Abstract

Immune checkpoint inhibitors (ICI)-based combinations have become the standard first-line treatment for advanced clear cell renal cell carcinoma (ccRCC). Despite significant improvements in survival and the achievement of sustained long-term responses, a subset of patients remains refractory to ICI, and most will eventually develop resistance. Thus, identifying predictive biomarkers for ICI efficacy and resistance is essential for optimizing therapeutic strategies. Up to now, tissue-based biomarkers have not been successful as predictive biomarkers in RCC. Circulating blood-based biomarkers offer a promising alternative. These biomarkers, including circulating immune cells, soluble factors, tumor-derived markers, and those based on metabolomics, are less invasive, offer reproducibility over time, and provide a comprehensive assessment of tumor biology and patient immune status, as well as allow dynamic monitoring during treatment. This review aims to evaluate the current evidence on the different candidate circulating biomarkers being investigated for their potential to predict ICI efficacy in RCC patients.

预测免疫检查点抑制剂对肾细胞癌疗效的血液循环生物标志物。
基于免疫检查点抑制剂(ICI)的联合疗法已成为晚期透明细胞肾细胞癌(ccRCC)的标准一线治疗方法。尽管生存率有了明显改善,并实现了持续的长期应答,但仍有一部分患者对 ICI 不耐受,而且大多数患者最终会产生耐药性。因此,确定 ICI 疗效和耐药性的预测性生物标志物对于优化治疗策略至关重要。到目前为止,基于组织的生物标志物还不能成功地作为 RCC 的预测性生物标志物。基于循环血液的生物标志物提供了一种很有前景的替代方法。这些生物标志物包括循环免疫细胞、可溶性因子、肿瘤衍生标志物以及基于代谢组学的生物标志物,它们的侵入性较低,在一段时间内具有可重复性,可对肿瘤生物学和患者免疫状态进行全面评估,并可在治疗过程中进行动态监测。本综述旨在评估目前正在研究的不同候选循环生物标志物的相关证据,以了解它们预测 RCC 患者 ICI 疗效的潜力。
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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来源期刊
CiteScore
2.80
自引率
0.00%
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0
审稿时长
13 weeks
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