Evidence map›Paper›PMID 35239968›Full record

Trial reportJournal of Crohn's & colitis2022

Efficacy and Safety of Maintenance Ustekinumab for Ulcerative Colitis Through 3 Years: UNIFI Long-term Extension.

Maria T Abreu, David S Rowbotham, Silvio Danese, William J Sandborn, Ye Miao, Hongyan Zhang, Ilia Tikhonov, Remo Panaccione, Tadakazu Hisamatsu, Ellen J Scherl and 6 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of Crohn's & colitis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07240168 (Drug Retention in Vedolizumab-treated Patients With Active UC After the Addition of Adjunct CurQD), which is not on this map. Cited by 50 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 3 pooled it
–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.

NCT07240168 active not recruitingnot on this mapstarted 2025, after this paper: background citation

Drug Retention in Vedolizumab-treated Patients With Active UC After the Addition of Adjunct CurQD: A Retrospective Cohort Study

TypeobservationalSponsorEvinature Ltd.Ran2025 to 2026Enrolled400ConditionsUlcerative Colitis (UC)ArmsCurQD (Curcumin + QingDai combination)
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Hepatitis B Virus Reactivation Risk With IL-17, IL-23/IL-12, or JAK Inhibitors: A Systematic Review and Meta-Analysis.Liver international : official journal of the International Association for the Study of the Liver · 2026
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  7. [Advanced Combination Therapy in Inflammatory Bowel Disease].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 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

16 authors.

Maria T AbreuDivision of Gastroenterology, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL, USA.
David S RowbothamDepartment of Gastroenterology & Hepatology, Auckland City Hospital, Auckland, New Zealand.
Silvio DaneseGastroenterology and Endoscopy, IRCCS Ospedale San Raffaele and University Vita-Salute San Raffaele, Milano, Italy.
William J SandbornDivision of Gastroenterology, University of California San Diego, La Jolla, CA, USA.
Ye MiaoJanssen Research & Development LLC., Immunology, Spring House, PA, USA.
Hongyan ZhangJanssen Research & Development LLC., Immunology, Spring House, PA, USA.
Ilia TikhonovJanssen Research & Development LLC., Immunology, Spring House, PA, USA.
Remo PanaccioneInflammatory Bowel Disease Unit, Division of Gastroenterology and Hepatology, University of Calgary, Calgary, AB, Canada.
Tadakazu HisamatsuDepartment of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Ellen J ScherlJill Roberts Center for Inflammatory Bowel Disease, New York Presbyterian Weill Cornell Medical College, New York, NY, USA.
Rupert W LeongGastroenterology and Liver Services Concord Hospital and Department of Gastroenterology Macquarie University Hospital, Sydney, NSW, Australia.
Ramesh P ArasaradnamDepartment of Gastroenterology, University Hospital Coventry & Warwickshire NHS Trust, Coventry, UK.
Waqqas AfifDivision of Gastroenterology, McGill University Health Centre, Montreal, QC, Canada.
Laurent Peyrin-BirouletUniversity of Lorraine, CHRU-Nancy, Department of Gastroenterology and Nutrition, Genetics, and Environmental Risk Exposure, Nancy, France.
Bruce E SandsDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Colleen MaranoJanssen Research & Development LLC., Immunology, Spring House, PA, USA.

Funding

Janssen Research & Development, LLC
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe UNIFI long-term extension [LTE] study reports the efficacy and safety of subcutaneous 90 mg ustekinumab through 3 years of maintenance therapy.

methodsPatients randomised to ustekinumab every 12 weeks [q12w] or every 8 weeks [q8w] at maintenance baseline [N = 348] and randomised ustekinumab-treated patients in the LTE [N = 284] were evaluated. Symptomatic remission [Mayo stool frequency = 0/1, rectal bleeding = 0] was assessed. Safety included all LTE patients [N = 188 placebo and N = 457 ustekinumab].

resultsAmong patients randomised to the ustekinumab q12w and q8w groups at maintenance baseline, 54.1% and 56.3% achieved symptomatic remission at Week 152, respectively. Overall, 20% of patients discontinued ustekinumab, 10% of biologic-naïve and 30% of biologic-exposed patients. Among patients in symptomatic remission at Year 3, 94.6% and 98.0% of patients were also corticosteroid free, respectively. Corticosteroid-free symptomatic remission rates in the ustekinumab q12w and q8w groups were 51.2% and 55.1% at Week 152, respectively. Remission rates were higher for biologic-naïve patients than for those with a history of biologic failure. Biochemical evidence of response was demonstrated by stable, decreased C-reactive protein and faecal calprotectin measurements over 3 years. From Weeks 96 to 156, no deaths, major adverse cardiovascular events, or tuberculosis occurred. Nasopharyngitis, ulcerative colitis, and upper respiratory tract infection were most frequently reported. One ustekinumab-treated patient with a history of basal cell carcinoma [BCC] reported two BCCs. One patient in the q8w ustekinumab group, who was receiving concomitant 6-mercaptopurine, experienced serious adverse events of neutropenic sepsis and oral herpes.

conclusionsEfficacy of ustekinumab in patients with ulcerative colitis was confirmed through 3 years. No new safety signals were observed.

Indexed as

Biological ProductsColitis, UlcerativeHumansRemission InductionTreatment OutcomeUstekinumabBiological ProductsUstekinumabsymptomatic remissionulcerative colitisUstekinumab

Identifiers

PMID35239968
PMCPMC9426670

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Registered trials

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.