Evidence map›Paper›PMID 36793598›Full record

ArticleFrontiers in oncology2023

Development of a population pharmacokinetics and pharmacodynamics model of glucarpidase rescue treatment after high-dose methotrexate therapy.

Yutaka Fukaya, Toshimi Kimura, Yukihiro Hamada, Kenichi Yoshimura, Hiroaki Hiraga, Yuki Yuza, Atsushi Ogawa, Junichi Hara, Katsuyoshi Koh, Atsushi Kikuta and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Trial
  2. Article
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 11 institutions in 1 country.

Yutaka FukayaDepartment of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo, Japan.
Toshimi KimuraDepartment of Pharmacy, Juntendo University Hospital, Tokyo, Japan.
Yukihiro HamadaDepartment of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo, Japan.
Kenichi YoshimuraCenter for Integrated Medical Research, Hiroshima University Hospital, Hiroshima, Japan.
Hiroaki HiragaDepartment of Musculoskeletal Oncology, National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan.
Yuki YuzaDepartment of Hematology and Oncology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Atsushi OgawaDepartment of Pediatrics, Niigata Cancer Center Hospital, Niigata, Japan.
Junichi HaraDepartment of Pediatric Hematology/Oncology, Osaka City General Hospital, Osaka, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Atsushi KikutaDepartment of Pediatric Oncology, Fukushima Medical College, Fukushima, Japan.
Yuhki KogaDepartment of Perinatal and Pediatric Medicine, Kyushu University, Fukuoka, Japan.
Hiroshi KawamotoDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tokyo Women's Medical University Hospital · JPHiroshima University Hospital · JPImperial Household Agency · JPJuntendo University Hospital · JPKyushu University · JPNational Cancer Center Hospital East · JPNational Hospital Organization Hokkaido Medical Center · JPNiigata Cancer Center Hospital · JPOsaka City General Hospital · JPSaitama Children's Medical Center · JPTokyo Metropolitan Children's Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Glucarpidase (CPG2) reduces the lethal toxicity of methotrexate (MTX) by rapid degradation. Methods: In this study, a CPG2 population pharmacokinetics (popPK) analysis in healthy volunteers (phase 1 study) and a popPK-pharmacodynamics (popPK-PD) analysis in patients (phase 2 study, Results: The population mean PK parameters (95% CI) of MTX, obtained from the final model Discussion: These results suggest that the pre-CPG2 dose and 24 h after CPG2 dosing were the most important sampling points in the Bayesian estimation of plasma MTX concentration prediction at 48 h. These CPG2-MTX popPK analysis and Bayesian estimation of rebound in plasma MTX concentrations are clinically important to estimate >1.0 μmol/L 48 h after the first CPG2 dosing. Clinical trial registration: https://dbcentre3.jmacct.med.or.jp/JMACTR/App/JMACTRS06/JMACTRS06.aspx?seqno=2363, identifier JMA-IIA00078 and https://dbcentre3.jmacct.med.or.jp/JMACTR/App/JMACTRS06/JMACTRS06.aspx?seqno=2782, identifier JMA-IIA00097.

Indexed as

glucarpidasemethotrexate - adverse effectspharmacodynamicspharmacokineticssafety

Identifiers

PMID36793598
PMCPMC9924065
OpenAlexW4318479870

What OpenQuestion holds

Textmetadata
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.