Evidence map›Paper›PMID 40312795›Full record

ArticleColorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland2025

A pilot study of gut mucosal and faecal microbiota in rectal cancer: associations with histological response and adverse events following preoperative chemoradiotherapy.

Shigenobu Emoto, Ryo Inoue, Shin Murai, Yuriko Inagaki, Hiroaki Nozawa, Kazuhito Sasaki, Koji Murono, Kensuke Kaneko, Yuichiro Yokoyama, Shinya Abe and 9 more

Abstract read
In one paragraph

Article in Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland, 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. Review
  2. Review
  3. Review
  4. A pilot study of gut mucosal and faecal microbiota in rectal cancer: associations with histological response and adverse events following preoperative chemoradiotherapy.Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland · 2025
    Article
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

19 authors.

Shigenobu EmotoDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.ORCID 0000-0002-6146-9385
Ryo InoueLaboratory of Animal Science, Setsunan University, Hirakata, Japan.
Shin MuraiDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Yuriko InagakiDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Hiroaki NozawaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Kazuhito SasakiDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Koji MuronoDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.ORCID 0000-0002-4184-5443
Kensuke KanekoDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Yuichiro YokoyamaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Shinya AbeDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Yuzo NagaiDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Takahide ShinagawaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Yuichi TachikawaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Satoshi OkadaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.
Takamitsu TsukaharaKyoto Institute of Nutrition and Pathology, Ujitawara, Japan.
Kai OhashiKyoto Institute of Nutrition and Pathology, Ujitawara, Japan.
Masashi OhnoDepartment of Gastroenterology, Shiga University of Medical Science, Otsu, Japan.
Akira AndohDepartment of Gastroenterology, Shiga University of Medical Science, Otsu, Japan.
Soichiro IshiharaDepartment of Surgical Oncology, University of Tokyo, Tokyo, Japan.

Funding

Japan Society for the Promotion of Science
6 · The paper itself

Abstract

aimPreoperative chemoradiotherapy (CRT) is administered for locally advanced rectal cancer (LARC); however, its efficacy and toxicity vary among patients. This study aimed to elucidate the relationship between the gut microbiota and the effectiveness and adverse events of CRT.

methodsThis prospective study included 21 patients with LARC with no history of antibiotic or probiotic administration for 6 months. Tumour mucosa, non-tumour mucosa and faecal samples were collected before and after CRT, and bacterial DNA was extracted. Metataxonomic analysis targeting the V3 and V4 regions of the 16S rRNA gene was conducted to determine the diversity and composition of the microbiota. Linear discriminant analysis effect size (LEfSe) was used to explore potential bacterial taxa predicting pathological complete response (pCR) and treatment-associated diarrhoea, which are major adverse events of CRT.

resultsAmong the 21 patients, five achieved pCR and seven experienced severe treatment-associated diarrhoea. There were no significant differences in α-diversity and β-diversity of the microbiota between the groups at any sampling sites before or after CRT. Exploratory analysis using LEfSe identified Peptostreptococcus, Coprococcus and Phoceaicola in the tumour mucosa before CRT as significant indicators for achieving pCR. Additionally, Collinsella, Haemophilus and Desulfovibrionaceae are associated with treatment-associated diarrhoea. Microbiome composition changed before and after CRT, with a notable decrease in the genus Fusobacterium_C and other taxa. β-diversity in the tumour area also changed significantly (P = 0.03).

conclusionsThis study suggests an association between the gut microbiota, the therapeutic effectiveness of CRT and the occurrence of treatment-associated diarrhoea in rectal cancer. These results indicate the potential for predicting treatment efficacy and adverse events based on the microbiota composition.

Indexed as

ChemoradiotherapyFecesGastrointestinal MicrobiomeIntestinal MucosaRectal NeoplasmsAgedDiarrheaFemaleHumansMaleMiddle AgedNeoadjuvant TherapyPilot ProjectsProspective StudiesRNA, Ribosomal, 16STreatment OutcomeRNA, Ribosomal, 16Schemoradiotherapymicrobiotamucosal microbiomepathological complete responserectal cancertreatment‐associated diarrhoea

Identifiers

PMID40312795
PMCPMC12046106

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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.