Monocyte-related markers as predictors of immune checkpoint inhibitor efficacy and immune-related adverse events: a systematic review and meta-analysis.

IF 7.7 2区 医学 Q1 ONCOLOGY
Aiarpi Ezdoglian, Michel Tsang-A-Sjoe, Fatemeh Khodadust, George Burchell, Gerrit Jansen, Tanja de Gruijl, Mariette Labots, Conny J van der Laken
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引用次数: 0

Abstract

The efficacy and off-target effects of immune checkpoint inhibitors (ICI) in cancer treatment vary among patients. Monocytes likely contribute to this heterogeneous response due to their crucial role in immune homeostasis. We conducted a systematic review and meta-analysis to evaluate the impact of monocytes on ICI efficacy and immune-related adverse events (irAEs) in patients with cancer. We systematically searched PubMed, Web of Science, and Embase for clinical studies from January 2000 to December 2023. Articles were included if they mentioned cancer, ICI, monocytes, or any monocyte-related terminology. Animal studies and studies where ICIs were combined with other biologics were excluded, except for studies where two ICIs were used. This systematic review was registered with PROSPERO (CRD42023396297) prior to data extraction and analysis. Monocyte-related markers, such as absolute monocyte count (AMC), monocyte/lymphocyte ratio (MLR), specific monocyte subpopulations, and m-MDSCs were assessed in relation to ICI efficacy and safety. Bayesian meta-analysis was conducted for AMC and MLR. The risk of bias assessment was done using the Cochrane-ROBINS-I tool. Out of 5787 studies identified in our search, 155 eligible studies report peripheral blood monocyte-related markers as predictors of response to ICI, and 32 of these studies describe irAEs. Overall, based on 63 studies, a high MLR was a prognostic biomarker for short progression-free survival (PFS) and overall survival (OS) hazard ratio (HR): 1.5 (95% CI: 1.21-1.88) and 1.52 (95% CI:1.13-2.08), respectively. The increased percentage of classical monocytes was an unfavorable predictor of survival, while low baseline rates of monocytic myeloid-derived suppressor cells (m-MDSCs) were favorable. Elevated intermediate monocyte frequencies were associated but not significantly correlated with the development of irAEs. Baseline monocyte phenotyping may serve as a composite biomarker of response to ICI; however, more data is needed regarding irAEs. Monocyte-related variables may aid in risk assessment and treatment decision strategies for patients receiving ICI in terms of both efficacy and safety.

免疫检查点抑制剂(ICI)治疗癌症的疗效和脱靶效应因患者而异。由于单核细胞在免疫平衡中的关键作用,它们很可能是造成这种异质性反应的原因之一。我们进行了一项系统综述和荟萃分析,以评估单核细胞对癌症患者 ICI 疗效和免疫相关不良事件(irAEs)的影响。我们系统检索了 2000 年 1 月至 2023 年 12 月期间在 PubMed、Web of Science 和 Embase 上进行的临床研究。只要提及癌症、ICI、单核细胞或任何单核细胞相关术语的文章均被纳入。除使用两种 ICIs 的研究外,动物研究和 ICIs 与其他生物制剂联合使用的研究均被排除在外。在数据提取和分析之前,本系统综述已在 PROSPERO(CRD42023396297)上注册。评估了单核细胞相关指标,如单核细胞绝对计数(AMC)、单核细胞/淋巴细胞比值(MLR)、特定单核细胞亚群和 m-MDSCs 与 ICI 疗效和安全性的关系。对AMC和MLR进行了贝叶斯荟萃分析。偏倚风险评估采用 Cochrane-ROBINS-I 工具进行。在我们搜索到的 5787 项研究中,有 155 项符合条件的研究报告了外周血单核细胞相关标记物作为 ICI 反应的预测因子,其中 32 项研究描述了虹膜AEs。总体而言,基于 63 项研究,高 MLR 是无进展生存期(PFS)和总生存期(OS)危险比(HR)分别为 1.5(95% CI:1.21-1.88)和 1.52(95% CI:1.13-2.08)的预后生物标志物。经典单核细胞比例的增加对预测生存率不利,而单核细胞髓源性抑制细胞(m-MDSCs)基线比例低则对预测生存率有利。中间单核细胞频率升高与虹膜急性损伤的发生有关,但无显著相关性。基线单核细胞表型可作为 ICI 反应的综合生物标志物;但是,还需要更多有关虹膜不良反应的数据。单核细胞相关变量可能有助于接受 ICI 治疗的患者在疗效和安全性方面的风险评估和治疗决策策略。
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
17.00
自引率
0.00%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Contemporary biomedical research is on the threshold of an era in which physiological and pathological processes can be analyzed in increasingly precise and mechanistic terms.The transformation of biology from a largely descriptive, phenomenological discipline to one in which the regulatory principles can be understood and manipulated with predictability brings a new dimension to the study of cancer and the search for effective therapeutic modalities for this disease. Cancer and Metastasis Reviews provides a forum for critical review and discussion of these challenging developments. A major function of the journal is to review some of the more important and interesting recent developments in the biology and treatment of malignant disease, as well as to highlight new and promising directions, be they technological or conceptual. Contributors are encouraged to review their personal work and be speculative.
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