Trial reportBMC cancer2025
Effects of Bojungikki-Tang on immune response and clinical outcomes in NSCLC patients receiving immune checkpoint inhibitors: a randomized pilot study.
Trial report in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Current clinical applications and clinical evidence of Bojungikki-tang, a traditional East Asian multi-botanical preparation: a scoping review.Frontiers in pharmacology · 2026Pooled it
- Research progress on traditional Chinese medicine-assisted immune checkpoint inhibitors therapy for solid tumors.Frontiers in immunology · 2026Review
- Review
- Regulatory effects of traditional Chinese medicine on the breast-cancer immune microenvironment.Frontiers in immunology · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
backgroundCancer 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.
methodsTwenty-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).
resultsAEs 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.
conclusionsBJIKT 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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