Evidence map›Paper›PMID 33331142›Full record

ReviewClinical pharmacology in drug development2021

Assessment of Vedolizumab Disease-Drug-Drug Interaction Potential in Patients With Inflammatory Bowel Diseases.

Wan Sun, Richard A Lirio, Jennifer Schneider, Jiri Aubrecht, Harisha Kadali, Mike Baratta, Parul Gulati, Ajit Suri, Tiffany Lin, Raghavan Vasudevan and 1 more

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical pharmacology in drug development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Nutrients · 2023
    Article
  6. Article
  7. Review
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 at 2 institutions in 1 country.

Wan SunTakeda, Cambridge, Massachusetts, USA.
Richard A LirioTakeda, Cambridge, Massachusetts, USA.
Jennifer SchneiderCertara USA, Inc., Princeton, New Jersey, USA.
Jiri AubrechtTakeda, Cambridge, Massachusetts, USA.
Harisha KadaliTakeda, Cambridge, Massachusetts, USA.
Mike BarattaTakeda, Cambridge, Massachusetts, USA.
Parul GulatiTakeda, Cambridge, Massachusetts, USA.
Ajit SuriTakeda, Cambridge, Massachusetts, USA.
Tiffany LinCertara USA, Inc., Princeton, New Jersey, USA.
Raghavan VasudevanTakeda, Cambridge, Massachusetts, USA.
Maria RosarioTakeda, Cambridge, Massachusetts, USA.
Takeda (United States) · USIntegra LifeSciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease-drug-drug interactions (DDDIs) have been identified in some inflammatory diseases in which elevated proinflammatory cytokines can downregulate the expression of cytochrome P450 (CYP) enzymes, potentially increasing systemic exposure to drugs metabolized by CYPs. Following anti-inflammatory treatments, CYP expression may return to normal, resulting in reduced drug exposure and diminished clinical efficacy. Vedolizumab has a well-established positive benefit-risk profile in patients with ulcerative colitis (UC) or Crohn's disease (CD) and has no known systemic immunosuppressive activity. A stepwise assessment was conducted to evaluate the DDDI potential of vedolizumab to impact exposure to drugs metabolized by CYP3A through cytokine modulation. First, a review of published data revealed that patients with UC or CD have elevated cytokine concentrations relative to healthy subjects; however, these concentrations remained below those reported to impact CYP expression. Exposure to drugs metabolized via CYP3A also appeared comparable between patients and healthy subjects. Second, serum samples from patients with UC or CD who received vedolizumab for 52 weeks were analyzed and compared with healthy subjects. Cytokine concentrations and the 4β-hydroxycholesterol-to-cholesterol ratio, an endogenous CYP3A4 biomarker, were comparable between healthy subjects and patients both before and during vedolizumab treatment. Finally, a medical review of postmarketing DDDI cases related to vedolizumab from the past 6 years was conducted and did not show evidence of any true DDDIs. Our study demonstrated the lack of clinically meaningful effects of disease or vedolizumab treatment on the exposure to drugs metabolized via CYP3A through cytokine modulation in patients with UC or CD.

Indexed as

Antibodies, Monoclonal, HumanizedCase-Control StudiesColitis, UlcerativeCrohn DiseaseCytochrome P-450 CYP3ACytokinesDatabases, FactualDrug InteractionsGastrointestinal AgentsHumansRandomized Controlled Trials as TopicRetrospective StudiesAntibodies, Monoclonal, HumanizedCYP3A protein, humanCytochrome P-450 CYP3ACytokinesGastrointestinal Agentsvedolizumabbiologicsclinical pharmacologydisease managementdrug-drug interactionsgastrointestinal

Identifiers

PMID33331142
PMCPMC8359401
OpenAlexW3112415592

What OpenQuestion holds

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LicenceCC BY
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.