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

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:一项随机对照试验

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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.

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