Evidence map›Paper›PMID 41315998›Full record

Observational studyBMC gastroenterology2025

Insights into the treatment of infliximab and vedolizumab in positive PR3-ANCA patients with moderately to severely active ulcerative colitis: multicenter real-world evidence.

Qi Yu, Yiyu Cheng, Fang Liu, Yidong Chen, Jiamin Li, Xiaopeng Zhang, Xiaoyu Fu, Junrong Li, Liangru Zhu

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC gastroenterology, 2025. 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

9 authors.

Qi Yu *Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yiyu Cheng *Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Fang Liu *Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yidong Chen *Department of Endoscopy and Digestive System, Guizhou Provincial People's Hospital, Guiyang, China.
Jiamin LiDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xiaopeng ZhangDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xiaoyu FuDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Junrong LiDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Liangru ZhuDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. zhuliangru@hust.edu.cn.

Funding

Key Technologies Research and Development Program 2018YFC0114600National Natural Science Foundation of China 82170547
6 · The paper itself

Abstract

BACKGROUND AND

aimsPerinuclear anti-neutrophil cytoplasmic antibody(p-ANCA) positivity may indicate poor response to infliximab (IFX) in ulcerative colitis (UC). Nevertheless, there has been limited research on the effect of proteinase 3 anti-neutrophil cytoplasmic antibody (PR3-ANCA) in UC patients treated with IFX and vedolizumab (VDZ). This study aimed to investigate the short-term efficacy of PR3-ANCA in patients with moderate-to-severe active UC.

methodsA total of 191 patients with moderate to severe active UC were enrolled from January 2021 to January 2024 in three centers in this retrospective, multicenter, real-world, case-control study. Patients with PR3-ANCA were allocated to two groups based on the biologics regimen (IFX or VDZ). Additionally, UC patients without positive PR3-ANCA, who were matched for baseline covariates including age, sex, BMI, disease duration, disease location, Mayo endoscopic subscore(MES), and prior advanced therapies, were selected at a ratio of 1:3. Clinical remission (CRm) and response (CRs), and endoscopic response (ERs) and remission(ERm) at week 22 were the endpoints.

resultsCompared to UC patients with negative PR3-ANCA, those with positive PR3-ANCA had lower rates of CRm (47.44% vs. 23.08%, P = 0.029), ERs (57.69% vs. 34.62%, P = 0.041), and ERm (39.74% vs. 11.54%, P = 0.008), but similar rates of CRs (69.23% vs. 65.38%, P = 0.715). However, there are no significant differences in rates of CRm (30.00% vs. 29.82%, P = 0.986), CRs (63.33% vs. 63.16%, P = 0.987), ERs (33.33% vs. 35.09%, P = 0.870), and ERm (20.00% vs. 21.05%, P = 0.908) between VDZ-treated patients with positive PR3-ANCA and negative. Additionally, compared to VDZ-treated patients, those treated with IFX had similar rates in CRm (30.00% vs. 23.08%, P = 0.560), CRs (63.33% vs. 65.38%, P = 0.873), ERs (33.33% vs. 34.62%, P = 0.920), and ERm (20.00% vs. 11.54%, P = 0.481). Rates in CRm (47.44% vs. 29.82%, P = 0.039), ERs (57.69% vs. 35.09%, P = 0.009), and ERm (39.74% vs. 21.05%, P = 0.021) in IFX-treated patients with negative PR3-ANCA were significantly higher than those in the VDZ-treated patients, but CRs was similar (69.23% vs. 63.16%, P = 0.460).

conclusionsPositive PR3-ANCA affects the efficacy of IFX rather than VDZ in patients with moderate to severe active UC. UC patients with positive PR3-ANCA results may benefit from the exploration of new treatment strategies.

Indexed as

Antibodies, Antineutrophil CytoplasmicAntibodies, Monoclonal, HumanizedColitis, UlcerativeGastrointestinal AgentsInfliximabMyeloblastinAdultCase-Control StudiesFemaleHumansMaleMiddle AgedRemission InductionRetrospective StudiesSeverity of Illness IndexTreatment OutcomeAntibodies, Antineutrophil CytoplasmicAntibodies, Monoclonal, HumanizedGastrointestinal AgentsInfliximabMyeloblastinvedolizumabAnti-neutrophil cytoplasmic antibodyInfliximabReal-world studyUlcerative colitisVedolizumab

Identifiers

PMID41315998
PMCPMC12751131

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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.