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补中益气汤对接受免疫检查点抑制剂治疗的非小细胞肺癌患者免疫反应和临床结局的影响:一项随机试验研究

Effects of Bojungikki-Tang on immune response and clinical outcomes in NSCLC patients receiving immune checkpoint inhibitors: a randomized pilot study.

作者信息

Ko Mi Mi, Na Se Won, Yi Jin-Mu, Jang Ho, Choi Chang Min, Lee Seung Hyeun, Lee Sung Yong, Jeong Mi-Kyung

机构信息

KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.

KM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.

出版信息

BMC Cancer. 2025 Jul 29;25(1):1229. doi: 10.1186/s12885-025-14629-4.

Abstract

BACKGROUND

Cancer immunotherapy with immune checkpoint inhibitors (ICIs) is a pivotal treatment for cancers, including non-small cell lung cancer (NSCLC). ICIs are often associated with adverse events (AEs), including immune-related AEs (irAEs). Bojungikki-tang (BJIKT), a traditional herbal medicine, has immunomodulatory properties and may alleviate fatigue and inflammation in patients with advanced cancer.In this multicenter, randomized, placebo-controlled pilot trial, we evaluated the safety and potential effects of BJIKT on fatigue, muscle loss, and immune response in patients with advanced NSCLC undergoing atezolizumab monotherapy.

METHODS

Twenty-eight patients were randomized to either the BJIKT (n = 14) or placebo (n = 14) groups. Primary outcomes included AEs and irAEs, while secondary outcomes assessed fatigue and muscle loss. Exploratory immune profiling was performed on peripheral blood mononuclear cells and plasma samples from a subset of patients (BJIKT n = 12, placebo n = 7).

RESULTS

AEs occurred in 53.57% of participants, with 64.29% in the BJIKT group (23 events, including one severe irAE) and 42.86% in the placebo group (12 events). Most AEs were mild or moderate and resolved by the study's completion. The objective response rate was 16.67% in the BJIKT group and 8.33% in the placebo group, while the disease control rate was 41.67% and 25.0%, respectively; however, these differences were not statistically significant. BJIKT showed non-significant trends toward reducing fatigue and mitigating muscle-related symptoms. Immune profiling suggested that BJIKT may activated CD4 + T cells, increased the proportion of CD3 + CD4 + cells, and enhanced T cell function while reducing immune exhaustion. Notably, a statistically significant decrease in PD-1 + CD8 + T cells was observed, while the reduction in PD-1 + CD4 + T cells did not reach significance. Additionally, a significant increase in natural killer cell counts was observed in the BJIKT group, suggesting a possible improvement in innate immune surveillance. These exploratory immune trends, although largely not statistically significant, may point to potential synergy with ICIs in enhancing anti-tumor immunity in advanced NSCLC.

CONCLUSIONS

BJIKT may enhance immune response and potentially improve clinical outcomes in patients with NSCLC receiving immune checkpoint inhibitor therapy; however, these exploratory and mostly non-significant findings warrant cautious interpretation and further validation in larger trials.

TRIAL REGISTRATIONS

The trial was registered with the Clinical Research Information Service ( https://cris.nih.go.kr/cris ; identifier number: KCT0006689) in October 2021.

摘要

背景

使用免疫检查点抑制剂(ICI)的癌症免疫疗法是包括非小细胞肺癌(NSCLC)在内的多种癌症的关键治疗方法。ICI常常与不良事件(AE)相关,包括免疫相关不良事件(irAE)。补中益气汤(BJIKT)是一种传统草药,具有免疫调节特性,可能缓解晚期癌症患者的疲劳和炎症。在这项多中心、随机、安慰剂对照的试点试验中,我们评估了BJIKT对接受阿替利珠单抗单药治疗的晚期NSCLC患者的疲劳、肌肉损失和免疫反应的安全性及潜在影响。

方法

28名患者被随机分为BJIKT组(n = 14)或安慰剂组(n = 14)。主要结局包括AE和irAE,次要结局评估疲劳和肌肉损失。对一部分患者(BJIKT组n = 12,安慰剂组n = 7)的外周血单核细胞和血浆样本进行探索性免疫分析。

结果

53.57%的参与者发生了AE,BJIKT组为64.29%(23起事件,包括1起严重irAE),安慰剂组为42.86%(12起事件)。大多数AE为轻度或中度,在研究结束时得到缓解。BJIKT组的客观缓解率为16.67%,安慰剂组为8.33%,疾病控制率分别为41.67%和25.0%;然而,这些差异无统计学意义。BJIKT在减轻疲劳和缓解肌肉相关症状方面显示出不显著的趋势。免疫分析表明,BJIKT可能激活CD4 + T细胞,增加CD3 + CD4 +细胞的比例,增强T细胞功能,同时减少免疫耗竭。值得注意的是,观察到PD - 1 + CD8 + T细胞有统计学意义的减少,而PD - 1 + CD4 + T细胞的减少未达到显著水平。此外,可以观察到BJIKT组自然杀伤细胞计数显著增加,表明先天免疫监视可能得到改善。这些探索性免疫趋势虽然大多无统计学意义,但可能表明在增强晚期NSCLC的抗肿瘤免疫方面与ICI有潜在协同作用。

结论

BJIKT可能增强接受免疫检查点抑制剂治疗的NSCLC患者的免疫反应,并可能改善临床结局;然而,这些探索性且大多无统计学意义的发现需要谨慎解读,并在更大规模试验中进一步验证。

试验注册

该试验于2021年10月在临床研究信息服务中心(https://cris.nih.go.kr/cris;标识符编号:KCT0006689)注册。

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