Evidence map›Paper›PMID 40731270›Full record

Trial reportBMC cancer2025

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

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

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mi Mi Ko *KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.
Se Won Na *KM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.
Jin-Mu YiKM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.
Ho JangKM Data Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea.
Chang Min ChoiDepartment of Pulmonary and Critical Care Medicine, Department of Oncology, Medical Center, College of Medicine, University of Ulsan, Seoul, 05505, Republic of Korea.
Seung Hyeun LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kyung Hee University Hospital, Kyung Hee University College of Medicine, Seoul, 02447, Republic of Korea.
Sung Yong LeeDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, 08308, Republic of Korea. syl0801@korea.ac.kr.
Mi-Kyung JeongKM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon, 34054, Republic of Korea. oiny2000@kiom.re.kr.

Funding

Korea Institute of Oriental Medicine (KIOM) KSN2322240
6 · The paper itself

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.

Indexed as

Carcinoma, Non-Small-Cell LungDrugs, Chinese HerbalImmune Checkpoint InhibitorsLung NeoplasmsAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedFatigueFemaleHumansMaleMiddle AgedPilot ProjectsTreatment OutcomeAntibodies, Monoclonal, HumanizedatezolizumabDrugs, Chinese HerbalImmune Checkpoint InhibitorsBojungikki-tangImmune checkpoint inhibitorsImmune profilingNon-small cell lung cancerPBMCs analysis

Identifiers

PMID40731270
PMCPMC12306011

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.