Evidence map›Paper›PMID 25884529›Full record

ReviewPharmacotherapy2015

Vedolizumab for the treatment of moderately to severely active ulcerative colitis.

Parambir S Dulai, Mahmoud Mosli, Reena Khanna, Barrett G Levesque, William J Sandborn, Brian G Feagan

Erratum issuedAbstract readReview
In one paragraph

Review in Pharmacotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Observational
  4. Article
  5. Article
  6. Review
  7. Article
  8. Fungal Infections and New Biologic Therapies.Current rheumatology reports · 2016
    Review
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Parambir S DulaiRobarts Clinical Trials, Robarts Research Institute, Western University, London, Ontario, Canada; Division of Gastroenterology, University of California San Diego, La Jolla, California.
Mahmoud Mosli
Reena Khanna
Barrett G Levesque
William J Sandborn
Brian G Feagan

Funding

Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
NIDDK NIH HHS 5T32DK007202-39NIDDK NIH HHS T32 DK007202
6 · The paper itself

Abstract

Ulcerative colitis is a chronic, idiopathic, inflammatory bowel disease characterized by a relapsing and remitting course. A substantial proportion of patients fail conventional therapies despite therapy with immunosuppressives and tumor necrosis factor antagonists. Accordingly, newer therapeutic agents that target disease-specific inflammation and minimize adverse events are required. Central to the pathogenesis of ulcerative colitis is an aberrant host response to commensal microorganisms with a resultant dysregulation of gut immune homeostasis and lymphocyte trafficking. Recently, a newer biologic, vedolizumab, which blocks lymphocyte trafficking, has been developed for use in moderate to severe ulcerative colitis. The efficacy of this agent has been demonstrated to be similar to that of other currently available biologics, and the selectivity of this agent in blocking lymphocyte migration to the gut has substantially reduced treatment-related adverse events. The drug has now been approved for use in the United States and Europe, and, although the exact positioning of this biologic in clinical practice is yet to be defined, it represents an important new chapter in our armamentarium of treatment options for this population. In this review, we will highlight key considerations to be made by providers when using this agent in clinical practice.

Indexed as

Antibodies, Monoclonal, HumanizedBacterial InfectionsCell Adhesion MoleculesCell MovementClinical Trials as TopicColitis, UlcerativeDrug Therapy, CombinationHumansImmunosuppressive AgentsIntegrinsLeukoencephalopathy, Progressive MultifocalNatalizumabNeoplasmsT-LymphocytesTumor Necrosis Factor-alphaAntibodies, Monoclonal, HumanizedCell Adhesion MoleculesImmunosuppressive Agentsintegrin alpha4beta7IntegrinsNatalizumabTumor Necrosis Factor-alphavedolizumabinflammatory bowel diseasemucosal addressin cell adhesion molecule-1ulcerative colitisvedolizumabα4β7

Identifiers

PMID25884529
PMCPMC6709861

What OpenQuestion holds

Textmetadata
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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.