Evidence map›Paper›PMID 29079637›Full record

ArticleThe oncologist2018

Consensus Guideline for Use of Glucarpidase in Patients with High-Dose Methotrexate Induced Acute Kidney Injury and Delayed Methotrexate Clearance.

Laura B Ramsey, Frank M Balis, Maureen M O'Brien, Kjeld Schmiegelow, Jennifer L Pauley, Archie Bleyer, Brigitte C Widemann, David Askenazi, Sharon Bergeron, Anushree Shirali and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in The oncologist, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05899751 (High-dose Methotrexate Patterns of Use, Clearance, Toxicities, Supportive Care and Outcomes), which is not on this map. Cited by 105 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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.

NCT05899751 unknown statusnot on this mapstarted 2022, after this paper: background citation

High-dose Methotrexate Patterns of Use, Clearance, Toxicities, Supportive Care and Outcomes

TypeobservationalSponsorProtherics Medicines Development LimitedRan2022 to 2024Enrolled1,000ConditionsAcute Kidney Injury, Drug ToxicityArmsHigh-dose methotrexate, Glucarpidase
3 · Its place in the literature

Who cites it

105 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Oral regimen for high dose methotrexate urine alkalinization: a systematic review and meta-analysis.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2024
    Pooled it
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45 more citing papers are in PubMed but not listed here.

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.

Laura B RamseyDivision of Research in Patient Services, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA laura.ramsey@cchmc.org.
Frank M BalisCenter for Childhood Cancer Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Maureen M O'BrienDivision of Oncology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Kjeld SchmiegelowDepartment of Pediatrics and Adolescent Medicine, University Hospital Rigshospitalet, and Institute of Clinical Medicine, Faculty of Medicine, University of Copenhagen, Copenhagen, Denmark.
Jennifer L PauleyPharmaceutical Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Archie BleyerDepartment of Radiation Medicine, Oregon Health and Science University, Portland, Oregon, USA.
Brigitte C WidemannPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
David AskenaziPediatric and Infant Center for Acute Nephrology, Professor of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Sharon BergeronHyundai Cancer Institute, Children's Hospital of Orange County, Orange, California, USA.
Anushree ShiraliAssistant Professor of Medicine, Section of Nephrology, Yale University School of Medicine, New Haven, Connecticut, USA.
Stefan SchwartzMedizinische Klinik mit Schwerpunkt Hämatologie, Onkologie und Tumorimmunologie, Charité Campus Benjamin Franklin, Berlin, Germany.
Alexander A VinksDivision of Research in Patient Services, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Jesper HeldrupChildhood Cancer and Research Unit, University Children's Hospital, Lund, Sweden.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Therapies for patients with rare tumors and genetic tumor predispositionZIASC010354 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WIDEMANN, BRIGITTE · 2009 to 2025
$19.2M
NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

Acute kidney injury due to high-dose methotrexate (HDMTX) is a serious, life-threatening toxicity that can occur in pediatric and adult patients. Glucarpidase is a treatment approved by the Food and Drug Administration for high methotrexate concentrations in the context of kidney dysfunction, but the guidelines for when to use it are unclear. An expert panel was convened to provide specific, expert consensus guidelines for the use of glucarpidase in patients who develop HDMTX-induced nephrotoxicity and delayed methotrexate excretion. The guideline provides recommendations to identify the population of patients who would benefit from glucarpidase rescue by more precisely defining the absolute methotrexate concentrations associated with risk for severe or life-threatening toxicity at several time points after the start of an HDMTX infusion. For an HDMTX infusion ≤24 hours, if the 36-hour concentration is above 30 µM, 42-hour concentration is above 10 µM, or 48-hour concentration is above 5 µM and the serum creatinine is significantly elevated relative to the baseline measurement (indicative of HDMTX-induced acute kidney injury), glucarpidase may be indicated. After a 36- to 42-hour HDMTX infusion, glucarpidase may be indicated when the 48-hour methotrexate concentration is above 5 µM. Administration of glucarpidase should optimally occur within 48-60 hours from the start of the HDMTX infusion, because life-threatening toxicities may not be preventable beyond this time point. IMPLICATIONS FOR PRACTICE: Glucarpidase is a rarely used medication that is less effective when given after more than 60 hours of exposure to high-dose methotrexate, so predicting early which patients will need it is imperative. There are no currently available consensus guidelines for the use of this medication. The indication on the label does not give specific methotrexate concentrations above which it should be used. An international group of experts was convened to develop a consensus guideline that was specific and evidence-based to identify the population of patients who would benefit from glucarpidase.

Indexed as

Acute Kidney InjuryAntimetabolites, AntineoplasticConsensusDose-Response Relationship, DrugFollow-Up Studiesgamma-Glutamyl HydrolaseHumansMethotrexateNeoplasmsPractice Guidelines as TopicRecombinant ProteinsAntimetabolites, Antineoplasticgamma-Glutamyl HydrolaseglucarpidaseMethotrexateRecombinant ProteinsAcute kidney injuryCreatinineGlucarpidaseLeucovorinMethotrexate

Identifiers

PMID29079637
PMCPMC5759822

What OpenQuestion holds

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Registered trials

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.