Evidence map›Paper›PMID 38146999›Full record

ArticleNeuro-oncology2024

Consensus framework for conducting phase I/II clinical trials for children, adolescents, and young adults with pediatric low-grade glioma: Guidelines established by the International Pediatric Low-Grade Glioma Coalition Clinical Trial Working Group.

Sabine Mueller, Jason Fangusaro, Arzu Onar Thomas, Thomas S Jacques, Pratiti Bandopadhayay, Peter de Blank, Roger J Packer, Maryam Fouladi, Antoinette Schouten van Meeteren, David Jones and 8 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. RAS/MAPK inhibition in pediatric gliomas.Neuro-oncology advances · 2026
    Review
  3. Article
  4. Paediatric low-grade glioma: the role of classical pathology in integrated diagnostic practice.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 14 institutions in 7 countries.

Sabine MuellerDepartment of Neurology, Neurological Surgery and Pediatrics, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0002-3452-5150
Jason FangusaroDepartment of Hematology and Oncology, Children's Healthcare of Atlanta and Emory University, Atlanta, Georgia, USA.
Arzu Onar ThomasDepartment of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
Thomas S JacquesUCL Great Ormond Street Institute of Child Health and Histopathology Department, Developmental Biology and Cancer Programme, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Pratiti BandopadhayayDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.ORCID 0000-0002-4175-4760
Peter de BlankDepartment of Pediatrics, University of Cincinnati Medical Center and Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0001-6623-3040
Roger J PackerBrain Tumor Institute, Washington DC, USA.
Maryam FouladiPediatric Brain Tumor Program, Division of Hematology, Oncology, and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, Ohio, USA.ORCID 0000-0002-5693-035X
Antoinette Schouten van MeeterenPrincess Màxima Center for Pediatric Oncology, Department of Neuro-oncology, Utrecht, The Netherlands.
David JonesHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Arie PerryDepartments of Pathology and Neurological Surgery, University of California San Francisco, San Francisco, California, USA.
Yoshiko NakanoDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, Canada.
Darren HargraveDepartment of Paediatric Oncology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
David RiedlDepartment of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, University Hospital of Psychiatry II, Medical University of Innsbruck, Innsbruck, Austria.
Nathan J RobisonDivision of Hematology and Oncology, Children's Hospital Los Angeles, Los Angeles, California, USA.
Marita PartanenDepartment of Research, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Michael J FisherDivision of Oncology, Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Olaf WittHopp Children's Cancer Center (KiTZ), National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ) and University Hospital, Heidelberg, Germany.
Great Ormond Street Hospital for Children NHS Foundation Trust · GBPrincess Máxima Center · NLUniversity of California, San Francisco · USBroad Institute · USChildren's Hospital of Philadelphia · USCincinnati Children's Hospital Medical Center · USEmory University · USGerman Cancer Research Center · DEHopp Children's Cancer Center Heidelberg · DEHospital for Sick Children · CAInnsbruck Medical University · ATNationwide Children's Hospital · USSt. Jude Children's Research Hospital · USUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Within the last few decades, we have witnessed tremendous advancements in the study of pediatric low-grade gliomas (pLGG), leading to a much-improved understanding of their molecular underpinnings. Consequently, we have achieved successful milestones in developing and implementing targeted therapeutic agents for treating these tumors. However, the community continues to face many unknowns when it comes to the most effective clinical implementation of these novel targeted inhibitors or combinations thereof. Questions encompassing optimal dosing strategies, treatment duration, methods for assessing clinical efficacy, and the identification of predictive biomarkers remain unresolved. Here, we offer the consensus of the international pLGG coalition (iPLGGc) clinical trial working group on these important topics and comment on clinical trial design and endpoint rationale. Throughout, we seek to standardize the global approach to early clinical trials (phase I and II) for pLGG, leading to more consistently interpretable results as well as enhancing the pace of novel therapy development and encouraging an increased focus on functional endpoints as well and quality of life for children faced with this disease.

Indexed as

Antineoplastic AgentsBrain NeoplasmsGliomaAdolescentChildClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicConsensusHumansPractice Guidelines as TopicQuality of LifeTreatment OutcomeYoung AdultAntineoplastic AgentsConsensus recommendationEarly phase clinical trialLow grade glioma

Identifiers

PMID38146999
PMCPMC10912006
OpenAlexW4390237156

What OpenQuestion holds

Textmetadata
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.