Evidence map›Paper›PMID 40721426›Full record

ArticleNPJ biofilms and microbiomes2025

Gut microbiota and SCFAs improve the treatment efficacy of chemotherapy and immunotherapy in NSCLC.

Yanping Yang, Maosong Ye, Yijun Song, Wenyu Xing, Xing Zhao, Yufan Li, Jiacheng Shen, Jian Zhou, Kinji Arikawa, Shengdi Wu and 2 more

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–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

23 citing papers in PubMed.

  1. Review
  2. Propionate promotes CD8Journal for immunotherapy of cancer · 2026
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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

12 authors.

Yanping Yang *Shanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, China.
Maosong Ye *Department of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Yijun Song *Department of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Wenyu XingAcademy for Engineering and Technology, Fudan University, Shanghai, China.
Xing ZhaoDepartment of Pulmonary and Critical Care Medicine, The Third People's Hospital of Pingxiang City, Pingxiang, Jiangxi Province, China.
Yufan LiDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Jiacheng ShenDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Jian ZhouDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Kinji ArikawaJohn H Stroger Jr Hospital of Cook County, Chicago, IL, USA.
Shengdi WuDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, China. wu.shengdi@zs-hospital.sh.cn.
Yuanlin SongShanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, China. song.yuanlin@zs-hospital.sh.cn.
Nuo XuDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China. xu.nuo@zs-hospital.sh.cn.

Funding

Clinical Research Plan of SHDC SHDC2020CR5010-002National Key R&D Plan 2020YFC2003700National Natural Science Foundation of China 81401877, 82130001, and 82272243Science and Technology Commission of Shanghai Municipality 20Z11901000, 20DZ2261200, 20XD1401200, 22Y11900800Shanghai Municipal Health Commission and Shanghai Municipal Administrator of Traditional Chinese Medicine ZY(2021-2023)-0207-01Shanghai Municipal Key Clinical Specialty shslczdzk02201Shanghai Municipal Science and Technology Major Project ZD2021CY001
6 · The paper itself

Abstract

The role of gut dysbiosis in shaping immunotherapy responses is well-recognized, yet its effect on the therapeutic efficacy of chemotherapy and immunotherapy combinations remains poorly understood. We analyzed gut microbiota in non-small cell lung cancer (NSCLC) patients treated with chemo-immunotherapy, comparing responders and non-responders using 16S rRNA sequencing. Responders showed higher microbial richness and abundance of specific genera like Faecalibacterium and Subdoligranulum, and the phylum Firmicutes. Support vector machine (SVM), a machine learning model based on microbial composition, predicted treatment efficacy with the area under the curve (AUC) values of 0.763 for genera and 0.855 for species. Metagenomic analysis revealed significant differences in metabolic pathways, with responders exhibiting higher short-chain fatty acids (SCFAs) production. Fecal microbiota transplantation (FMT) and SCFAs supplementation in mouse models enhanced treatment efficacy by promoting effector T cell activity in tumors. Our study suggests that gut microbiota, through SCFAs production, regulates chemo-immunotherapy efficacy, offering new strategies to improve NSCLC treatment outcomes.

Indexed as

BacteriaCarcinoma, Non-Small-Cell LungFatty Acids, VolatileGastrointestinal MicrobiomeImmunotherapyLung NeoplasmsAgedAnimalsAntineoplastic AgentsDysbiosisFecal Microbiota TransplantationFemaleHumansMaleMetagenomicsMiceAntineoplastic AgentsFatty Acids, VolatileRNA, Ribosomal, 16S

Identifiers

PMID40721426
PMCPMC12304354

What OpenQuestion holds

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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.