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Record W2790809756 · doi:10.1093/ecco-jcc/jjx180.830

P703 Clinical, radiographic and endoscopic remission with vedolizumab treatment in Crohn’s disease

2018· article· en· W2790809756 on OpenAlexaffabout
Paulo Gustavo Kotze, Chaoran Ma, Abdulelah Almutairdi, A Al-Damarki, Shane Devlin, Gilaad G. Kaplan, Cynthia H. Seow, Kerri L. Novak, Cathy Lu, Jose G. Ferraz, Michael J. Stewart, Michelle Buresi, M. Mathivanan, Humberto Jijon, Joan Heatherington, M Martin, Remo Panaccione

Bibliographic record

VenueJournal of Crohn s and Colitis · 2018
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicInflammatory Bowel Disease
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsMedicineVedolizumabInternal medicineCrohn's diseaseGastroenterologyClinical trialUlcerative colitisSurgeryRetrospective cohort studyEndoscopyDisease

Abstract

fetched live from OpenAlex

Vedolizumab (VDZ) is a gut-specific α-4-β-7 integrin antagonist that has demonstrated efficacy in randomised controlled trials to induce and maintain clinical response and remission in moderate-to-severe Crohn’s disease (CD) randomised controlled trials. The aim of this study was to evaluate the symptomatic and objective response and remission rates achieved with VDZ therapy in CD in a large tertiary care cohort. A retrospective cohort study was performed at the University of Calgary with adult (≥18 years) CD patients receiving VDZ induction between 2012 and 2017. The primary outcome was clinical or objective remission at 3, 6, and 12 months after induction. Clinical remission was defined by complete absence of symptoms and no need for corticosteroids. Objective remission was defined by steroid-free endoscopic mucosal healing or complete normalisation of radiographic appearance on contrast-enhanced ultrasound or CT/MR enterography. A total of 122 patients were included. Mean follow-up was 43.4 weeks (SD 30.8 weeks). Sixty-nine percent (84/122) of patients had previously failed anti-TNF therapy; 18.9% (23/122) had failed at least 3 previous biologic therapies. Steroid-free clinical remission at 3, 6 and 12 months was 19.8% (22/111), 22.1% (21/95), and 22.1% (15/68), respectively. Steroid-free endoscopic or radiographic remission occurred in 11.5% (6/52), 21.2% (14/66), and 18.9% (7/37) patients at 3, 6, and 12 months, respectively. Mucosal healing on endoscopy was achieved by 22.2% (6/27), 33.3% (14/42), and 25.9% (7/27) of patients at 3, 6, and 12 months, respectively. 109 CD patients with symptomatic response within 6 months to VDZ induction therapy were followed for a mean duration of 46.3 weeks (SD ± 31.3 weeks). Composite loss of response occurred in 36 patients (33.0%) in follow-up at a mean time of 35.2 weeks (± 20.9 weeks). Adverse events (AE) were reported in 35 patients (28.7%). The most common AE were infections (16/122, 6.6%) and infusion reactions (8/122, 6.6%). Serious adverse events were reported in 8 patients (6.6%). Two deaths occurred in the cohort: one patient developed cholangiocarcinoma (pre-existing primary sclerosing cholangitis) and a second patient died from metastatic renal cell carcinoma (diagnosed prior to initiation of VDZ). Clinical and objective (endoscopic or radiographic) response and remission with vedolizumab In this cohort of patients with highly refractory CD, VDZ was effective for inducing steroid-free clinical, endoscopic, and radiographic remission. Loss of response to VDZ occurred in one-third of patients and approximately 20% will discontinue treatment.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.004
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.011

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.004
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.011
GPT teacher head0.281
Teacher spread0.269 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2018
Admission routes2
Has abstractyes

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