Evidence map›Paper›PMID 29788240›Full record

ArticleInflammatory bowel diseases2018

Predictors and Management of Loss of Response to Vedolizumab in Inflammatory Bowel Disease.

Eugenia Shmidt, Gursimran Kochhar, Justin Hartke, Prianka Chilukuri, Joseph Meserve, Khadija Chaudrey, Jenna L Koliani-Pace, Robert Hirten, David Faleck, Morris Barocas and 22 more

Abstract read
In one paragraph

Article in Inflammatory bowel diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 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.

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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Therapeutic Drug Monitoring of Vedolizumab Levels During Maintenance in Inflammatory Bowel Disease (MOVE-IBD).JGH open : an open access journal of gastroenterology and hepatology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Refractory Crohn's Disease: Perspectives, Unmet Needs and Innovations.Clinical and experimental gastroenterology · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Observational
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Eugenia ShmidtIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Gursimran KochharCleveland Clinic Foundation, Cleveland, OH, USA.
Justin HartkeIndiana University, Indianapolis, IN, USA.
Prianka ChilukuriIndiana University, Indianapolis, IN, USA.
Joseph MeserveUniversity of California, San Diego, La Jolla, CA, USA.
Khadija ChaudreyMayo Clinic, Rochester, MN, USA.
Jenna L Koliani-PaceDartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Robert HirtenIcahn School of Medicine at Mount Sinai, New York, NY, USA.
David FaleckIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Morris BarocasTakeda Pharmaceuticals USA Inc., Deerfield, IL, USA.
Michelle LuoTakeda Pharmaceuticals USA Inc., Deerfield, IL, USA.
Karen LaschTakeda Pharmaceuticals USA Inc., Deerfield, IL, USA.
Brigid S BolandUniversity of California, San Diego, La Jolla, CA, USA.
Siddharth SinghUniversity of California, San Diego, La Jolla, CA, USA.
Niels Vande CasteeleUniversity of California, San Diego, La Jolla, CA, USA.
Sashidhar Varma SagiIndiana University, Indianapolis, IN, USA.
Monika FischerIndiana University, Indianapolis, IN, USA.
Shannon ChangNew York University (NYU), New York, NY, USA.
Matthew BohmIndiana University, Indianapolis, IN, USA.
Dana LukinMontefiore Medical Center, New York, NY, USA.
Keith SultanNorth Shore University Hospital, Manhasset, NY, USA.
Arun SwaminathLenox Hill Hospital, New York, NY, USA.
David HudesmanNew York University (NYU), New York, NY, USA.
Nitin GuptaUniversity of Mississippi, Jackson, MS, USA.
Sunanda KaneMayo Clinic, Rochester, MN, USA.
Edward V LoftusMayo Clinic, Rochester, MN, USA.
William J SandbornUniversity of California, San Diego, La Jolla, CA, USA.
Corey A SiegelDartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Bruce E SandsIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Jean-Frederic ColombelIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Bo ShenCleveland Clinic Foundation, Cleveland, OH, USA.
Parambir S DulaiUniversity of California, San Diego, La Jolla, CA, USA.

Funding

UC San Diego Clinical and Translational Research InstituteKL2TR001444 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEPP, COLIN A. · 2015 to 2024
$15.4M
Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
Comparative Risks and Benefits of Pharmacological Therapies for Older Patients with Inflammatory Bowel DiseasesK23DK117058 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SINGH, SIDDHARTH · 2018 to 2022
$971k
NCATS NIH HHS KL2 TR001444NIDDK NIH HHS K23 DK117058NIDDK NIH HHS T32 DK007202
6 · The paper itself

Abstract

Background: We quantified loss of response (LOR) to vedolizumab (VDZ) in clinical practice and assessed the effectiveness of VDZ dose intensification for managing LOR. Methods: Retrospective review (May 2014-December 2016) of a prospectively maintained inflammatory bowel disease (IBD) registry. Kaplan-Meier estimates were used to determine rates of LOR to VDZ . Independent predictors of LOR were identified using univariate and multivariable Cox proportional hazard regression. Success of recapturing response (>50% reduction in symptoms from baseline) and remission (complete resolution of symptoms) after dose intensification was quantified. Results: Cumulative rates for VDZ LOR were 20% at 6 months and 35% at 12 months, with slightly lower rates in Crohn's disease than in ulcerative colitis (6 months 15% vs 18% and 12 months 30% vs 39%, P = 0.03). On multivariable analysis, LOR to a tumor necrosis factor (TNF) antagonist before VDZ use was associated with an increased risk for LOR to VDZ [hazard ratio (HR) 1.93; 95% confidence interval (CI) 1.25-2.97] in all patients. For Crohn's disease patients specifically, higher baseline C-reactive protein concentration was associated with increased risk for LOR to VDZ (HR 1.01 per mg/dL increase, 95% CI 1.01-1.02). Shortening of VDZ infusion interval from 8 to every 4 or 6 weeks recaptured response in 49% and remission in 18% of patients. Conclusions: LOR to a TNF antagonist before VDZ use and higher baseline C-reactive protein are important predictors of VDZ LOR. Treatment response can be recaptured in almost half of these patients with VDZ infusion interval shortening.

Indexed as

Severity of Illness IndexAdultAntibodies, Monoclonal, HumanizedBiomarkersColitis, UlcerativeC-Reactive ProteinCrohn DiseaseDisease ManagementFemaleFollow-Up StudiesGastrointestinal AgentsHumansMaleMiddle AgedPrognosisProspective StudiesAntibodies, Monoclonal, HumanizedBiomarkersC-Reactive ProteinGastrointestinal Agentsvedolizumab

Identifiers

PMID29788240
PMCPMC6693035

What OpenQuestion holds

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Registered trials

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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.