← 返回前沿论文

昼夜节律对癌症患者免疫检查点抑制剂治疗的影响:最新临床综述

英文原题:Impact of time-of-day on immune checkpoint inhibitor therapy in cancer patients: an up-to-date clinical review.

查看英文原题

Impact of time-of-day on immune checkpoint inhibitor therapy in cancer patients: an up-to-date clinical review.

PubMed 2026/05/29(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Bacalam C、Puscariu I、Sur D、Burz C
第一作者单位
Department of Head and Neck Oncology, Gustave Roussy, Villejuif, France.France
通讯作者单位
Department of Medical Oncology, The Oncology Institute "Prof. Dr. Ion Chiricuţă", Cluj-Napoca, Romania.Italy
文献类型
综述
期刊
Frontiers in immunology2026
原文标识
PubMed 42292486 · DOI 10.3389/fimmu.2026.1837812