Evidence map›Paper›PMID 28250007›Full record

ArticleHaematologica2017

Population pharmacokinetics of intravenous Erwinia asparaginase in pediatric acute lymphoblastic leukemia patients.

Sebastiaan D T Sassen, Ron A A Mathôt, Rob Pieters, Robin Q H Kloos, Valérie de Haas, Gertjan J L Kaspers, Cor van den Bos, Wim J E Tissing, Maroeska Te Loo, Marc B Bierings and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 27 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

13 authors at 10 institutions in 1 country.

Sebastiaan D T SassenDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands.
Ron A A MathôtDepartment of Hospital Pharmacy, Academic Medical Center, University of Amsterdam, the Netherlands.
Rob PietersPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Robin Q H KloosDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands.
Valérie de HaasDutch Childhood Oncology Group, The Hague, the Netherlands.
Gertjan J L KaspersPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Cor van den BosDepartment of Pediatric Oncology, Emma Children's Hospital, Academic Medical Center, Amsterdam, the Netherlands.
Wim J E TissingDepartment of Pediatric Oncology, Beatrix Children's Hospital, University Medical Center, Groningen, the Netherlands.
Maroeska Te LooDepartment of Pediatric Hemato-Oncology, Radboud University Nijmegen Medical Center, the Netherlands.
Marc B BieringsPediatric Blood and Marrow Transplantation Program, University Medical Center Utrecht/Wilhelmina Children's Hospital, the Netherlands.
Wouter J W KollenDepartment of Pediatric Immunology, Hemato-Oncology and Stem Cell Transplantation, Leiden University Medical Center, the Netherlands.
Christian M ZwaanDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands.
Inge M van der SluisDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands i.vandersluis@erasmusmc.nl.
Erasmus MC - Sophia Children’s Hospital · NLAcademic Medical Center · NLAmsterdam UMC Location VUmc · NLEmma Kinderziekenhuis · NLLeiden University Medical Center · NLPrincess Máxima Center · NLRadboud University Nijmegen · NLStichting Kinderoncologie Nederland · NLUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erwinia asparaginase is an important component in the treatment of pediatric acute lymphoblastic leukemia. A large variability in serum concentrations has been observed after intravenous Erwinia asparaginase. Currently, Dutch Childhood Oncology Group protocols dose alterations are based on trough concentrations to ensure adequate asparaginase activity (≥100 IU/L). The aim of this study was to describe the population pharmacokinetics of intravenous Erwinia asparaginase to quantify and gather insight into inter-individual and inter-occasion variability. The starting dose was evaluated on the basis of the derived population pharmacokinetic parameters. In a multicenter prospective observational study, a total of 714 blood samples were collected from 51 children (age 1-17 years) with acute lymphoblastic leukemia. The starting dose was 20,000 IU/m

Indexed as

Administration, IntravenousAdolescentAntineoplastic AgentsAsparaginaseChildChild, PreschoolFemaleHumansInfantMaleModels, StatisticalPopulation SurveillancePrecursor Cell Lymphoblastic Leukemia-LymphomaReproducibility of ResultsAntineoplastic AgentsAsparaginase

Identifiers

PMID28250007
PMCPMC5394946
OpenAlexW2554250866

What OpenQuestion holds

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LicenceCC BY-NC
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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.