Evidence map›Paper›PMID 40111550›Full record

ArticleCancer chemotherapy and pharmacology2025

Alternative routes of drug administration: exposure of imatinib using different formulations.

H B Fiebrich-Westra, O Visser, A B Francken, E J Smolders

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Article in Cancer chemotherapy and pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

H B Fiebrich-WestraDepartment of Hematology and Medical Oncology, Isala Hospital, Zwolle, The Netherlands.
O VisserDepartment of Hematology and Medical Oncology, Isala Hospital, Zwolle, The Netherlands.
A B FranckenDepartment of Surgical Oncology, Isala Hospital, Zwolle, The Netherlands.
E J SmoldersDepartment of Clinical Pharmacy, Isala Hospital, Dr. van Heesweg 2, Zwolle, 8025AB, The Netherlands. E.J.Smolders@isala.nl.ORCID http://orcid.org/0000-0001-5694-9758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo explore the possibility of treating patients with alternative imatinib formulations.

methodsTwo patients were treated with different enteral en rectal imatinib formulations. During treatment plasma concentrations where measured to assure adequate exposure.

resultsThe first patient received imatinib suspension through the duodenum tube. With a dose of 400 mg BID the patient had an imatinib plasma concentration of 750 µg/L. After increasing the dose to 600 mg BID the imatinib plasma concentration was 1500 µg/L (target GIST treatment > 1100 µg/L). Rectal administration of the tablet did not lead to sufficient plasma concentrations. The second had adequate exposure of imatinib both when the suspension was taken orally and through the tube (target CML treatment are > 1000 µg/L).

conclusionFor patients able to swallow liquids, we prefer the suspended imatinib tablets (comparable to drug label). If patients have a duodenum tube the use of a suspension base with pulverized tablets could be an alternative. Based on the extremely low exposure found in case 1, we do not recommend rectal administration of tablets. We recommend the monitor plasma concentrations when off label dosing forms are used.

Indexed as

Antineoplastic AgentsBenzamidesGastrointestinal Stromal TumorsPiperazinesPyrimidinesAdministration, OralAdministration, RectalChemistry, PharmaceuticalDrug Administration RoutesHumansImatinib MesylateSuspensionsTabletsAntineoplastic AgentsBenzamidesImatinib MesylatePiperazinesPyrimidinesSuspensionsTabletsDasatinibImatinibPharmacokineticsPharmacologyTherapeutic drug monitoring

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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.