通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
肿瘤细胞治疗研究
英文原题:Impact of time-of-day on immune checkpoint inhibitor therapy in cancer patients: an up-to-date clinical review.
Impact of time-of-day on immune checkpoint inhibitor therapy in cancer patients: an up-to-date clinical review.
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在过去十年中,免疫检查点抑制剂(ICIs)已成为多种癌症治疗的基石。多种因素影响ICI的疗效和毒性,当前研究正在探讨给药时间是否符合昼夜节律是否是其中之一。本综述的范围仅限于ICIs(抗CTLA-4、抗PD-1、抗PD-L1、抗LAG-3),不详细涉及其他免疫治疗方式(溶瘤病毒、细胞因子疗法、过继细胞转移、癌症疫苗)。
我们综合了相关研究结果,这些结果与昼夜节律在调节正常免疫功能中的作用一致,包括已报道的特定检查点分子和免疫细胞群活性的昼夜节律变化。多项研究(主要为回顾性研究)报道了当日较早时间输注ICI与更有利的疗效结局之间的关联;然而,证据基础具有异质性,且首个随机III期试验(目前受Nature Medicine编辑注关注)提示ICI给药的每日时间(ToD)可能与疗效差异相关,而毒性信号则更为异质。鉴于回顾性数据集中存在永生时间偏倚、周期数混杂和排程偏倚的风险,需要额外的多中心前瞻性随机试验来确定因果关系和可重复性,同时还需研究昼夜节律生物标志物,以帮助在常规临床护理中实现给药时间的个体化。
Over the last decade, immune checkpoint inhibitors (ICIs) have become a cornerstone of the treatment of multiple cancer types. Several factors influence ICI efficacy and toxicity, and current research is investigating whether circadian timing of administration is one of them. This review is limited in scope to ICIs (anti-CTLA-4, anti-PD-1, anti-PD-L1, anti-LAG-3) and does not detail other immunotherapeutic modalities (oncolytic viruses, cytokine therapies, adoptive cell transfer, cancer vaccines).
We synthesised the findings, which are consistent with a role for the circadian rhythm in modulating normal immune function, including reported circadian variation in the activity of specific checkpoint molecules and immune cell populations. Several studies, predominantly retrospective, have reported associations between earlier-in-the-day ICI infusion and more favourable efficacy outcomes; however, the evidence base is heterogeneous, and the first randomised phase III trial currently subject to a Nature Medicine Editor's Note suggests that time of day (ToD) of ICI administration may be associated with differences in efficacy, with more heterogeneous signals for toxicity.
Given the risk of immortal-time bias, cycle-number confounding and scheduling bias in retrospective datasets, additional multicentre prospective randomised trials are required to establish causality and reproducibility, alongside research into circadian biomarkers that could help personalise timing in routine clinical care.
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