Evidence map›Paper›PMID 41810446›Full record

ArticleWorld journal of gastroenterology2026

Comparable remission and health care use in real-world inflammatory bowel disease patients initiating originator biologics

Cristiano S Moura, Albert Etingin, Luck Lukusa, Harminder Singh, Neeraj Narula, Laura E Targownik, Yvette Leung, Petros Zezos, Beata Polewiczowska-Nowak, Waqqas Afif and 1 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in World journal of 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.

Cristiano S MouraCentre for Outcomes Research and Evaluation, The Research Institute of the McGill University Health Centre, Montreal H4A 3S5, Quebec, Canada.
Albert EtinginCore Internal Medicine Residency Program, Department of Medicine, McGill University, Montreal H4A 3J1, Quebec, Canada.
Luck LukusaCentre for Outcomes Research and Evaluation, The Research Institute of the McGill University Health Centre, Montreal H4A 3S5, Quebec, Canada.
Harminder SinghDepartment of Internal Medicine and Community Health Sciences, Max Rady College of Medicine, University of Manitoba, Winnipeg R3E 3P5, Manitoba, Canada.
Neeraj NarulaDepartment of Medicine and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton L8N 3ZN, Ontario, Canada.
Laura E TargownikDepartment of Medicine, University of Toronto, Toronto M5S 1A1, Ontario, Canada.
Yvette LeungDepartment of Medicine, University of British Columbia, Vancouver V6T 1Z4, British Columbia, Canada.
Petros ZezosNOSM University, Thunder Bay Regional Health Sciences Centre, Thunder Bay P7B 7A5, Ontario, Canada.
Beata Polewiczowska-NowakNOSM University, Thunder Bay Regional Health Sciences Centre, Thunder Bay P7B 7A5, Ontario, Canada.
Waqqas AfifDepartment of Medicine, McGill University, Montreal H4A 3J1, Quebec, Canada.
Sasha BernatskyCentre for Outcomes Research and Evaluation, The Research Institute of the McGill University Health Centre, Montreal H4A 3S5, Quebec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiologic therapies, including anti-tumor necrosis factor agents, have significantly improved the management of inflammatory bowel disease (IBD). However, their high cost can limit patient access. Biosimilars are a more affordable option than originator biologics and offer potential for improved accessibility, though real-world evidence comparing their effectiveness remains limited.

aimTo describe real-world, comparative outcomes of IBD patients taking biologics and biosimilars, focusing on remission and healthcare use.

methodsWe used data from a multicenter registry-based cohort, which includes participants from six Canadian IBD clinical centers. Adults with ulcerative colitis or Crohn's disease who initiated biosimilar, or originator formulations of infliximab or adalimumab were included. The primary outcome was clinical remission; secondary outcomes included hospitalizations and emergency department (ED) visits. Kaplan-Meier survival analyses and multivariable Cox regression models were used to assess time to these outcomes, adjusting for disease activity, treatment history, and demographic characteristics.

resultsA total of 258 individuals were analyzed (192 biosimilar initiators and 66 originator users). The median time to remission was similar between biosimilars (12.2 months) and originators (12.8 months). We did not detect difference in the likelihood of achieving remission when comparing biosimilar and originator treatments (adjusted hazard ratio: 1.49; 95% confidence interval: 0.96-2.32). Hospitalization and ED visit rates were also comparable. Corticosteroid use and prior hospitalizations were associated with increased hospitalization risk.

conclusionThis study suggests biosimilars and originators have similar remission, ED visits, and hospitalization in IBD. This reinforces confidence in their equivalence, improving access while supporting healthcare system sustainability.

Indexed as

Biological ProductsBiosimilar PharmaceuticalsColitis, UlcerativeCrohn DiseaseGastrointestinal AgentsPatient Acceptance of Health CareAdalimumabAdultCanadaEmergency Room VisitsEmergency Service, HospitalFemaleHospitalizationHumansInfliximabMaleAdalimumabBiological ProductsBiosimilar PharmaceuticalsGastrointestinal AgentsInfliximabAdalimumabBiosimilarsClinical remissionEmergency department visitsHospitalizationInflammatory bowel diseaseInfliximab

Identifiers

PMID41810446
PMCPMC12968563

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.