Evidence map›Paper›PMID 28649001›Full record

Trial reportEuropean journal of cancer (Oxford, England : 1990)2017

A European randomised controlled trial of the addition of etoposide to standard vincristine and carboplatin induction as part of an 18-month treatment programme for childhood (≤16 years) low grade glioma - A final report.

Astrid K Gnekow, David A Walker, Daniela Kandels, Susan Picton, Giorgio Perilongo, Jacques Grill, Tore Stokland, Per Eric Sandstrom, Monika Warmuth-Metz, Torsten Pietsch and 7 more

Erratum issued Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in European journal of cancer (Oxford, England : 1990), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT00276640 (Cooperative Multicenter Study for Children and Adolescents With Low Grade Glioma), which is not on this map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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.

NCT00276640 nacompletednot on this map

Cooperative Multicenter Study for Children and Adolescents With Low Grade Glioma

TypeinterventionalSponsorSociete Internationale d'Oncologie PediatriqueRan2004 to 2017Enrolled3,417ConditionsPrimary Central Nervous System NeoplasmsArmsvincristine, carboplatin, vincristine, carboplatin, etoposide, radiation therapy
3 · Its place in the literature

Who cites it

90 citing papers in PubMed, 1 synthesis or guideline pooled it, 149 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Everolimus for Children With Recurrent or Progressive Low-Grade Glioma: Results From the Phase II PNOC001 Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Trial
  4. Trial
  5. FDA Approval Summary: Dabrafenib in Combination with Trametinib for BRAFV600E Mutation-Positive Low-Grade Glioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  6. Article
  7. Article
  8. Review
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  13. Review
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30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 17 institutions in 7 countries.

Astrid K GnekowSwabian Children's Cancer Center, Klinikum Augsburg, Germany.
David A WalkerChildren's Brain Tumour Research Centre, University of Nottingham, UK. Electronic address: David.walker@nottingham.ac.uk.
Daniela KandelsChildren's Brain Tumour Research Centre, University of Nottingham, UK.
Susan PictonLeeds Children's Hospital, UK.
Giorgio PerilongoDivision of Pediatrics, University Hospital of Padua, Italy.
Jacques GrillInstitut Gustave Roussy, Paris, France.
Tore StoklandUniversity Hospital of North Norway, Norway.
Per Eric SandstromUmea University, Sweden.
Monika Warmuth-MetzDepartment of Neuro-radiology, University of Wurzberg, Germany.
Torsten PietschUniversity of Bonn Medical Centre, Germany.
Felice GiangasperoDepartment of Radiological, Oncological and Anatomo-pathological Sciences, University Sapienza Rome, Rome, Italy; IRCCS Neuromed, Pozzilli, Italy.
René SchmidtInstitute of Biostatistics and Clinical Research, University of Muenster, Germany.
Andreas FaldumInstitute of Biostatistics and Clinical Research, University of Muenster, Germany.
Denise KilmartinClinical Trials and Biostatistics Unit, IRCCS Istituto Oncologico Veneto, Padova, Italy.
Angela De PaoliClinical Trials and Biostatistics Unit, IRCCS Istituto Oncologico Veneto, Padova, Italy.
Gian Luca De SalvoClinical Trials and Biostatistics Unit, IRCCS Istituto Oncologico Veneto, Padova, Italy.
of the Low Grade Glioma Consortium and the participating centers
Nordic Society for Pediatric Hematology and Oncology · SEAssociazione Italiana Ematologia Oncologia Pediatrica · ITIstituto Oncologico Veneto · ITSociety of Paediatric Oncology and Haematology · DEInstitut Gustave Roussy · FRIstituto Neurologico Mediterraneo · ITMRC Biostatistics Unit · GBUniversity Hospital Augsburg · DEUniversity Hospital of North Norway · NOUniversity of Bonn · DEUniversity of Nottingham · GBUniversity of Padua · ITArcadia · USBrain Tumour Research · GBClinical Research Center Kiel · DEClovis Oncology (United Kingdom) · GBUmeå University · SE

Funding

Cancer Research UK 15958Cancer Research UK C13189/A13205
6 · The paper itself

Abstract

backgroundThe use of chemotherapy to manage newly diagnosed low grade glioma (LGG) was first introduced in the 1980s. One randomised trial has studied two- versus four-drug regimens with a duration of 12 months of treatment after resection.

methodsWithin the European comprehensive treatment strategy for childhood LGG, the International Society of Paediatric Oncology-Low Grade Glioma (SIOP LGG) Committee launched a randomised trial involving 118 institutions and 11 countries to investigate the addition of etoposide (100 mg/m

findingsNo differences between the two arms were found in term of survival and radiological response. Response and non-progression rates at 24 weeks for VC and VCE, were 46% versus 41%, and 93% versus 91% respectively; 5-year Progression-Free Survival (PFS) and Overall Survival (OS) were 46% (StDev 3.5) versus 45% (StDev 3.5) and 89% (StDev 2.1) versus 89% (StDev 2.1) respectively. Age and diencephalic syndrome are adverse clinical risk factors for PFS and OS. 5-year OS for patients in early progression at week 24 were 46% (StDev 13.8) and 49% (StDev 16.5) in the two arms, respectively.

interpretationThe addition of etoposide to VC did not improve PFS or OS. High non-progression rates at 24 weeks justify retaining VC as standard first-line therapy. Infants with diencephalic syndrome and early progression need new treatments to be tested. Future trials should use neurological/visual and toxicity outcomes and be designed to discriminate between the impact on disease outcomes of 'duration of therapy' and 'age at stopping therapy'.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBrain NeoplasmsCarboplatinChildChild, PreschoolEtoposideFemaleGliomaHumansInduction ChemotherapyInfantMaleSurvival AnalysisVincristineCarboplatinEtoposideVincristineChemotherapyChildhoodLow grade gliomaRandomised trial

Identifiers

PMID28649001
PMCPMC5517338
OpenAlexW2652551831

What OpenQuestion holds

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LicenceCC BY
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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.