Evidence map›Paper›PMID 27423645›Full record

Trial reportJournal of neuro-oncology2016

Relapse patterns and outcome after relapse in standard risk medulloblastoma: a report from the HIT-SIOP-PNET4 study.

Magnus Sabel, Gudrun Fleischhack, Stephan Tippelt, Göran Gustafsson, François Doz, Rolf Kortmann, Maura Massimino, Aurora Navajas, Katja von Hoff, Stefan Rutkowski and 6 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 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.

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

71 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Review
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  12. National multicentered retrospective review of salvage therapy for pediatric medulloblastoma: a Canadian experience.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Article
  13. Article
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  15. Molecular features reflect clinical outcomes after recurrence in medulloblastoma: a single-institution experience.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Article
  16. Review
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  18. Article
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11 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

16 authors.

Magnus SabelDepartment of Paediatrics, University of Gothenburg and Queen Silvia Children's Hospital, Gothenburg, Sweden. magnus.sabel@vgregion.se.ORCID 0000-0002-3072-657X
Gudrun FleischhackPaediatrics III, Division of Paediatric Haematology and Oncology, University Hospital of Essen, Essen, Germany.
Stephan TippeltPaediatrics III, Division of Paediatric Haematology and Oncology, University Hospital of Essen, Essen, Germany.
Göran GustafssonKarolinska Institutet, Stockholm, Sweden.
François DozDepartment of Paediatrics, Adolescent and Young Adults Oncology, Institut Curie and University Paris Descartes, Sorbonne Paris Cité, Paris, France.
Rolf KortmannDepartment of Radiooncology, University Hospital Leipzig, Leipzig, Germany.
Maura MassiminoFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Aurora NavajasBiocruces Health Research Institute, Universidad Del País Vasco/EHU, Bilbao, Spain.
Katja von HoffUniversity Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Stefan RutkowskiUniversity Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Monika Warmuth-MetzUniversity of Würzburg, Würzburg, Germany.
Steven C CliffordNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Torsten PietschDepartment of Neuropathology, University of Bonn, Bonn, Germany.
Barry PizerAlder Hey Children's Hospital, Liverpool, UK.
Birgitta LanneringDepartment of Paediatrics, University of Gothenburg and Queen Silvia Children's Hospital, Gothenburg, Sweden.
SIOP-E Brain Tumour Group

Funding

Cancer Research UK 13457
6 · The paper itself

Abstract

The HIT-SIOP-PNET4 randomised trial for standard risk medulloblastoma (MB) (2001-2006) included 338 patients and compared hyperfractionated and conventional radiotherapy. We here report the long-term outcome after a median follow up of 7.8 years, including detailed information on relapse and the treatment of relapse. Data were extracted from the HIT Group Relapsed MB database and by way of a specific case report form. The event-free and overall (OS) survival at 10 years were 76 ± 2 % and 78 ± 2 % respectively with no significant difference between the treatment arms. Seventy-two relapses and three second malignant neoplasms were reported. Thirteen relapses (18 %) were isolated local relapses in the posterior fossa (PF) and 59 (82 %) were craniospinal, metastatic relapses (isolated or multiple) with or without concurrent PF disease. Isolated PF relapse vs all other relapses occurred at mean/median of 38/35 and 28/26 months respectively (p = 0.24). Late relapse, i.e. >5 years from diagnosis, occurred in six patients (8 %). Relapse treatment consisted of combinations of surgery (25 %), focal radiotherapy (RT 22 %), high dose chemotherapy with stem cell rescue (HDSCR 21 %) and conventional chemotherapy (90 %). OS at 5 years after relapse was 6.0 ± 4 %. In multivariate analysis; isolated relapse in PF, and surgery were significantly associated with prolonged survival whereas RT and HDSCR were not. Survival after relapse was not related to biological factors and was very poor despite several patients receiving intensive treatments. Exploration of new drugs is warranted, preferably based on tumour biology from biopsy of the relapsed tumour.

Indexed as

Treatment OutcomeAdolescentAntineoplastic Agentsbeta CateninBrain NeoplasmsChildChild, PreschoolCombined Modality TherapyDisease-Free SurvivalFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMedulloblastomaMutationAntineoplastic Agentsbeta CateninCTNNB1 protein, humanMYCN protein, humanN-Myc Proto-Oncogene ProteinChemotherapyClinical trialMedulloblastomaPaediatricRadiotherapyRelapseSecondary tumoursSurvivalTreatment

Identifiers

PMID27423645
PMCPMC5020107

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Registered trials

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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.