Evidence map›Paper›PMID 41971848›Full record

ArticleJCO oncology advances2026

Preoperative Gut Microbiome in Patients With Colorectal Cancer: Potential for Fecal Biomarker-Based Recurrence Risk Prediction.

Anne E Petersen, Konstantina Zafeiropoulou, Mohammed Ghiboub, Claire P M van Helsdingen, Joop L M Konsten, Nicole D Bouvy, Jan H M B Stoot, Pieter J Tanis, Wouter J de Jonge, Joep P M Derikx

Abstract read
In one paragraph

Article in JCO oncology advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Anne E Petersen *Department of Pediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0009-0002-4435-0689
Konstantina Zafeiropoulou *Amsterdam Gastroenterology Endocrinology Metabolism Institute, Amsterdam University Medical Centers, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5061-4658
Mohammed GhiboubDepartment of Pediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Claire P M van HelsdingenDepartment of Pediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-6508-0214
Joop L M KonstenDepartment of Surgery, Viecuri Hospital, Venlo, the Netherlands.ORCID https://orcid.org/0000-0002-8803-1914
Nicole D BouvyDepartment of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.
Jan H M B StootDepartment of Surgery, Zuyderland Medical Center, Heerlen and Sittard-Geleen, the Netherlands.ORCID https://orcid.org/0000-0003-3178-0049
Pieter J TanisDepartment of Oncological and Gastrointestinal Surgery, Erasmus Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-3146-3310
Wouter J de JongeAmsterdam Gastroenterology Endocrinology Metabolism Institute, Amsterdam University Medical Centers, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-3241-1547
Joep P M DerikxDepartment of Pediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: While gut microbiome dysbiosis is known to play a role in colorectal cancer (CRC) initiation and progression, its role in CRC recurrence remains unclear. This study investigates whether the gut microbiome is associated with CRC recurrence. Patients and Methods: In a prospective observational cohort, preoperative fecal samples from patients with stage I to III CRC undergoing surgical resection were analyzed using 16S rRNA gene sequencing. Alpha diversity and beta diversity were compared between patients with and without recurrence, and differential abundance analyses were conducted to identify bacterial genera associated with recurrence risk. Results: Among 294 patients, 61 (21%) patients developed recurrence during a median follow-up of 56 months, with a median time to recurrence of 19 months. Alpha diversity did not differ between groups, but beta diversity analysis revealed significantly distinct microbial clustering in patients with recurrence, particularly those with locoregional recurrence. Differential abundance analysis identified five bacterial genera associated with locoregional recurrence ( Conclusion: Patients with CRC who develop locoregional recurrence exhibit a distinct preoperative fecal microbial composition compared with those without recurrence. Our findings provide novel insights into the role of the intestinal microenvironment in recurrence and identify

Identifiers

PMID41971848
PMCPMC7618991

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