Evidence map›Paper›PMID 35355137›Full record

ArticleCancer chemotherapy and pharmacology2022

Pharmacokinetics of metronomic temozolomide in cerebrospinal fluid of children with malignant central nervous system tumors.

Sören Büsker, Walter Jäger, Stefan Poschner, Lisa Mayr, Valentin Al Jalali, Johannes Gojo, Amedeo A Azizi, Sami Ullah, Muhammad Bilal, Lobna El Tabei and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer chemotherapy and pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Sören BüskerCenter for Pharmacology, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Walter JägerDepartment of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Vienna, Austria.
Stefan PoschnerDepartment of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Vienna, Austria.
Lisa MayrDepartment of Pediatric and Adolescent Medicine, Medical University of Vienna, Comprehensive Center for Pediatrics, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Valentin Al JalaliDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Johannes GojoDepartment of Pediatric and Adolescent Medicine, Medical University of Vienna, Comprehensive Center for Pediatrics, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Amedeo A AziziDepartment of Pediatric and Adolescent Medicine, Medical University of Vienna, Comprehensive Center for Pediatrics, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Sami UllahCenter for Pharmacology, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Muhammad BilalCenter for Pharmacology, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Lobna El TabeiCenter for Pharmacology, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Uwe FuhrCenter for Pharmacology, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Andreas PeyrlDepartment of Pediatric and Adolescent Medicine, Medical University of Vienna, Comprehensive Center for Pediatrics, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria. andreas.peyrl@meduniwien.ac.at.ORCID http://orcid.org/0000-0002-5736-8231
Medical University of Vienna · ATUniversity of Cologne · DEUniversity of Vienna · ATUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAlthough temozolomide is widely used in the treatment of childhood central nervous system (CNS) tumors, information on its pharmacokinetic profile in the brain or cerebrospinal fluid (CSF) is sparse. This study aimed at investigating whether measurable and clinically relevant concentrations of temozolomide are reached and maintained in CSF for continuous oral administration in pediatric patients. A population pharmacokinetic model was developed to quantify CSF penetration of temozolomide.

methodsEleven pediatric CNS tumor patients (aged 4-14 years) treated with oral temozolomide using a metronomic schedule (24-77 mg/m

resultsMedian temozolomide concentrations in plasma and CSF were 0.96 (range 0.24-5.99) µg/ml and 0.37 (0.06-1.76) µg/ml, respectively. A two-compartment model (central/plasma [1], CSF [2]) with first-order absorption, first-order elimination, and a transit compartment between CSF and plasma adequately described the data. Population mean estimates for clearance (CL) and the volume of distribution in the central compartment (V

conclusionMetronomic oral temozolomide penetrates into the CSF in pediatric patients, with even higher concentration levels compared to adults.

Indexed as

Central Nervous System NeoplasmsAdultAnimalsArea Under CurveChildChromatography, High Pressure LiquidHumansMacaca mulattaTemozolomideTemozolomideCentral nervous systemCerebrospinal fluidPediatricsPharmacokineticTemozolomide

Identifiers

PMID35355137
PMCPMC9054874
OpenAlexW4220812148

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.