Evidence map›Paper›PMID 41034258›Full record

ArticleNPJ breast cancer2025

Longitudinal changes in gut microbiota composition during endocrine therapy in hormone receptor-positive breast cancer patients.

Chung-Hsin Tsai, Wei-Ling Huang, Ying-Wen Su, Fang Lee, Chi-Chan Lee, Fang-Yi Li, Horng-Woei Yang, Chien-Yi Lu, Po-Sheng Yang

Abstract read
In one paragraph

Article in NPJ breast cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. The dialogue between breast cancer and microorganisms.Frontiers in cellular and infection microbiology · 2026
    Review
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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

9 authors.

Chung-Hsin TsaiDepartment of General Surgery, MacKay Memorial Hospital, Taipei, 104217, Taiwan.
Wei-Ling HuangDepartment of Medicine, Mackay Medical University, New Taipei, 252005, Taiwan.
Ying-Wen SuDepartment of Medicine, Mackay Medical University, New Taipei, 252005, Taiwan.
Fang LeeDepartment of General Surgery, MacKay Memorial Hospital, Taipei, 104217, Taiwan.
Chi-Chan LeeDepartment of General Surgery, MacKay Memorial Hospital, Taipei, 104217, Taiwan.
Fang-Yi LiDepartment of Medical Research, MacKay Memorial Hospital, New Taipei City, 251404, Taiwan.
Horng-Woei YangDepartment of Medical Research, MacKay Memorial Hospital, New Taipei City, 251404, Taiwan.
Chien-Yi LuTaipei Wego Private Senior High School, Taipei, 11254, Taiwan.
Po-Sheng YangDepartment of General Surgery, MacKay Memorial Hospital, Taipei, 104217, Taiwan. psyang@mmu.edu.tw.ORCID http://orcid.org/0000-0002-6226-2618

Funding

National Science and Technology Council NSTC 112-2321-B-195-001
6 · The paper itself

Abstract

This prospective study of 90 breast cancer patients examined gut microbiota composition relative to hormone receptor status and endocrine therapy changes. Initial analysis suggested hormone receptor-negative patients had higher Fusobacteriaceae and Fusobacterium abundance, while hormone receptor-positive patients showed Ruminiclostridium enrichment, though differences lacked statistical significance after correction. Hormone receptor-positive patients without lymph node metastasis demonstrated potentially greater microbial diversity, but associations were non-significant after multiple comparison correction. Longitudinal analysis of 52 hormone receptor-positive patients revealed the most robust finding: statistically significant Blautia increases after hormone therapy and aromatase inhibitor treatment. Tamoxifen showed trends toward increased Lachnospiraceae but lost significance after correction due to small sample size. LHRH agonist treatment demonstrated significant Dialister and Megasphaera increases. This study identified limited but robust associations between gut microbiota and endocrine treatments, with Blautia as the most consistently affected genus across multiple therapies, though most findings require validation in larger cohorts.

Identifiers

PMID41034258
PMCPMC12488989

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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.