Evidence map›Paper›PMID 42477587›Full record

SynthesisBMC gastroenterology2026

Meta-analysis: safety and efficacy of ustekinumab in pediatric inflammatory bowel disease patients with anti-TNF failure.

Zhaoyang Heng, Li Zhan, Yuhan Zhang, Keyou Xu, Meng Song, Kelei Zhao, Md Shoykot Jahan, Most Fatema Akter, Ping Lu, Yinghua Ji and 1 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

11 authors.

Zhaoyang HengFirst Clinical College, Henan Medical University, Xinxiang, Henan, China.
Li ZhanClinical Medical College, Southwest Medical University, Luzhou, Sichuan, China.
Yuhan ZhangThe Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Keyou XuFirst Clinical College, Henan Medical University, Xinxiang, Henan, China.
Meng SongDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Kelei ZhaoDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Md Shoykot JahanDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Most Fatema AkterDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Ping LuDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Yinghua JiDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Yanting LiuDepartment of Oncology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China. yanting.liu@foxmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsEvidence for ustekinumab (UST) in pediatric inflammatory bowel disease (IBD) is limited, particularly in patients who do not respond to anti-tumor necrosis factor (anti-TNF) therapy. We conducted a meta-analysis to evaluate the efficacy and safety of UST in pediatric IBD after anti-TNF failure.

methodsPubMed, Cochrane Library, Embase, and Web of Science were searched from inception through August 2025. We included studies reporting outcomes of UST in pediatric IBD patients with prior anti-TNF failure. Pooled estimates were calculated using fixed- or random-effects models according to heterogeneity (I

resultsFifteen studies including 653 pediatric patients were analyzed. Pooled clinical remission rates were 57% (95% CI, 28%-86%) at 8-16 weeks and 68% (95% CI, 58%-79%) at week 52. Steroid-free clinical remission was 44% (95% CI, 38%-49%) at 8-16 weeks and 58% (95% CI, 45%-70%) at week 52. The pooled endoscopic remission rate was 42% (95% CI, 35%-49%) and a biochemical remission rate of 63% (95% CI, 40%-87%). Adverse events occurred in 20% of patients (95% CI, 9%-30%), and serious adverse events occurred in 1% (95% CI, 0%-2%). At week 52, clinical remission rates were 69% in Crohn's disease (CD) and 65% in ulcerative colitis (UC).

conclusionIn pediatric IBD patients with prior anti-TNF failure, UST was associated with favorable pooled remission rates and an acceptable safety profile, although substantial inter-study heterogeneity warrants cautious interpretation. These findings support UST as a feasible therapeutic option in this refractory pediatric setting; while highly generalizable to pediatric CD, the findings for the UC subgroup offer important preliminary evidence that warrants cautious interpretation due to limited precision.

Indexed as

Inflammatory Bowel DiseasesUstekinumabAdolescentChildChild, PreschoolColitis, UlcerativeCrohn DiseaseHumansInfantRemission InductionTreatment FailureTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor-alphaUstekinumabAnti-TNF failureInflammatory bowel diseaseMeta-analysisPediatricUstekinumab

Identifiers

PMID42477587
PMCPMC13670571

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Registered trials

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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.