Evidence map›Paper›PMID 36051959›Full record

ArticleFrontline gastroenterology2022

Comparative effectiveness of a second-line biologic in patients with ulcerative colitis: vedolizumab followed by an anti-TNF versus anti-TNF followed by vedolizumab.

Charles Miller, Hanson Kwok, Paul Harrow, Roser Vega, Edward Seward, Shameer Mehta, Farooq Rahman, Sara McCartney, Ioanna Parisi, Samuel Hsiang Lim and 21 more

Open access · greenAbstract read
In one paragraph

Article in Frontline gastroenterology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 21% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Deletion of TNF in Winnie-International journal of molecular sciences · 2022
    Article
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

31 authors at 10 institutions in 1 country.

Charles MillerDepartment of Gastroenterology, University College Hospital, London, UK.ORCID 0000-0002-2068-4839
Hanson KwokDepartment of Gastroenterology, University College Hospital, London, UK.
Paul HarrowDepartment of Gastroenterology, University College Hospital, London, UK.
Roser VegaDepartment of Gastroenterology, University College Hospital, London, UK.
Edward SewardDepartment of Gastroenterology, University College Hospital, London, UK.ORCID 0000-0001-6626-8462
Shameer MehtaDepartment of Gastroenterology, University College Hospital, London, UK.
Farooq RahmanDepartment of Gastroenterology, University College Hospital, London, UK.
Sara McCartneyDepartment of Gastroenterology, University College Hospital, London, UK.ORCID 0000-0003-2438-6086
Ioanna ParisiDepartment of Gastroenterology, University College Hospital, London, UK.
Samuel Hsiang LimDepartment of Gastroenterology, Guy's and Thomas' Hospital, London, UK.
Esha SharmaDepartment of Gastroenterology, Guy's and Thomas' Hospital, London, UK.
Mark A SamaanDepartment of Gastroenterology, Guy's and Thomas' Hospital, London, UK.
Aaron BancilDepartment of Gastroenterology, Royal London Hospital, London, UK.
Klaartje Bel KokDepartment of Gastroenterology, Royal London Hospital, London, UK.
Ahmed ShalabiDepartment of Gastroenterology, West Middlesex Hospital, London, UK.
Emma L JohnstonDepartment of Gastroenterology, West Middlesex Hospital, London, UK.
Dev KatareyDepartment of Gastroenterology, Royal Free Hospital London, London, UK.
Nina TaherzadehDepartment of Gastroenterology, Royal Free Hospital London, London, UK.
Charles MurrayDepartment of Gastroenterology, Royal Free Hospital London, London, UK.
Mohammed Tauseef SharipDepartment of Gastroenterology, Lister Hospital, Stevenage, UK.
Martyn J CarterDepartment of Gastroenterology, Lister Hospital, Stevenage, UK.
Shiva T RadhakrishnanDepartments of Gastroenterology and Hepatology, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.ORCID 0000-0002-6403-263X
Simon PeakeDepartments of Gastroenterology and Hepatology, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.
Imran KhakooDepartments of Gastroenterology, Chelsea and Westminster Hospital, London, UK.
Mahmood WahedDepartments of Gastroenterology, Chelsea and Westminster Hospital, London, UK.
Sebastian PovlsenDepartment of Gastroenterology, King's College Hospital, London, UK.
Mehul PatelDepartment of Gastroenterology, King's College Hospital, London, UK.
Patrick DuBoisDepartment of Gastroenterology, King's College Hospital, London, UK.
Jemima FinkelDepartment of Gastroenterology, Whittington Hospital, London, UK.
Clive OnnieDepartment of Gastroenterology, Whittington Hospital, London, UK.
Stuart BloomDepartment of Gastroenterology, University College Hospital, London, UK.
University College Hospital · GBKing's College Hospital · GBSt Thomas' Hospital · GBThe Royal Free Hospital · GBChelsea and Westminster Hospital · GBImperial College Healthcare NHS Trust · GBLister Hospital · GBRoyal London Hospital · GBWest Middlesex University Hospital · GBWhittington Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sequential drug treatment with biological agents in ulcerative colitis (UC) is becoming increasingly complex. There are few studies comparing head-to-head outcomes in second-line treatments. The study assesses whether using anti-tumour necrosis factor (anti-TNF)-α therapy following the α4β7 integrin blocker vedolizumab (VDZ) or VDZ after an anti-TNF has more favourable clinical outcomes in UC in a real-world outpatient setting. Methods: Patients with UC who were exposed to first-line anti-TNF (adalimumab or infliximab) or VDZ who subsequently switched to the alternate class between May 2013 and August 2020 were identified by reviewing patient databases at 10 hospitals. Data were collected retrospectively using patient records. Baseline demographics, disease activity indices, biochemical markers, endoscopic Mayo score, colectomy rates, treatment persistence and urgent hospital utilisation composite endpoint (UHUC) rates were examined over a 52-week period. Results: Second-line week 52 treatment persistence was higher in the VDZ group (71/81, 89%) versus the anti-TNF group (15/34, 44%; p=0.0001), as were week 52 colectomy-free survival (VDZ: 77/80, 96%, vs anti-TNF: 26/32, 81%; p=0.009), week 52 UHUC survival (VDZ: 68/84, 81%, vs anti-TNF: 20/34, 59%; p=0.002) and week 52 corticosteroid-free clinical remission (CFCR) rates (VDZ: 22/34, 65%, vs anti-TNF: 4/20, 20%; p=0.001). Conclusion: Compared with second-line anti TNF usage, the VDZ second-line cohort had significantly higher 52-week treatment persistence, UHUC survival, higher colectomy-free survival rates and higher week 52 CFCR. These data suggest that VDZ is an effective biologic in UC as a second-line therapy after anti-TNF exposure. It highlights the effect of biological order on clinically important outcomes.

Indexed as

IBD clinicalinflammatory bowel diseaseulcerative colitis

Identifiers

PMID36051959
PMCPMC9380760
OpenAlexW4205642608

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.