Evidence map›Paper›PMID 32112275›Full record

ReviewClinical pharmacokinetics2020

Clinical Pharmacokinetics and Pharmacodynamics of Dasatinib.

Dominique Levêque, Guillaume Becker, Karin Bilger, Shanti Natarajan-Amé

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical pharmacokinetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 80 citations in OpenAlex.

  1. Trial
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  3. Review
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  7. Review
  8. Dasatinib: A Novel Etiology of Reversible Cerebellar Ataxia.Annals of Indian Academy of Neurology · 2026
    Article
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  11. Review
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  13. Review
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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

4 authors at 1 institution in 1 country.

Dominique LevêquePharmacy, Hôpital Hautepierre, Avenue Molière, 67000, Strasbourg, France. dominique.leveque@chru-strasbourg.fr.ORCID 0000-0002-7423-1130
Guillaume BeckerPharmacy, Hôpital Hautepierre, Avenue Molière, 67000, Strasbourg, France.
Karin BilgerHematology, Hôpital Hautepierre, Avenue Molière, 67000, Strasbourg, France.
Shanti Natarajan-AméHematology, Hôpital Hautepierre, Avenue Molière, 67000, Strasbourg, France.
Hôpital d'Hautepierre · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dasatinib is an oral, once-daily tyrosine kinase inhibitor used in the treatment of chronic myeloid leukaemia and Philadelphia chromosome-positive acute lymphoblastic leukaemia. Dasatinib is rapidly absorbed, with the time for maximal serum concentration varying between 0.25 and 1.5 h. Oral absorption is not affected by food. The absolute bioavailability of dasatinib in humans is unknown due to the lack of an intravenous formulation preventing calculation of the reference exposure. Dasatinib is eliminated through cytochrome P450 (CYP) 3A4-mediated metabolism, with a terminal half-life of 3-4 h. Based on total radioactivity, only 20% of the oral dose (100 mg) is recovered unchanged in faeces (19%, including potential non-absorption) and urine (1%) after 168 h. Dasatinib pharmacokinetics are not influenced by age (children, and adults up to 86 years of age), race and renal insufficiency. Dasatinib absorption is decreased by pH-modifying agents (antacids, H

Indexed as

Protein Kinase InhibitorsAntineoplastic AgentsBiological AvailabilityDasatinibDrug InteractionsHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAntineoplastic AgentsDasatinibProtein Kinase Inhibitors

Identifiers

PMID32112275
OpenAlexW3007045996

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.