Evidence map›Paper›PMID 38835160›Full record

ArticleNeuro-oncology2024

Risk factors for domain-specific neurocognitive outcome in pediatric survivors of a brain tumor in the posterior fossa-Results of the HIT 2000 trial.

Martin Mynarek, Anne Rossius, Anika Guiard, Holger Ottensmeier, Katja von Hoff, Denise Obrecht-Sturm, Lisa Bußenius, Carsten Friedrich, Andre O von Bueren, Nicolas U Gerber and 13 more

Abstract 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. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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

  1. Pooled it
  2. Trial
  3. Article
  4. A brief history of ependymoma.Neuro-oncology · 2026
    Review
  5. Review
  6. 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

23 authors.

Martin MynarekDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0003-3302-2719
Anne RossiusDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Anika GuiardDepartment of Pediatrics, University Hospital Rostock, Rostock, Germany.
Holger OttensmeierDepartment of Pediatric Hematology and Oncology, University Children's Hospital Wuerzburg, Wuerzburg, Germany.
Katja von HoffDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Denise Obrecht-SturmDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Lisa BußeniusDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0003-3888-1360
Carsten FriedrichDepartment for General Pediatrics and Pediatric Hematology and Oncology, University Children's Hospital Oldenburg, Oldenburg, Germany.
Andre O von BuerenDivision of Pediatric Oncology and Hematology, Department of Pediatrics, Gynecology and Obstetrics, University Hospital of Geneva, Geneva, Switzerland.ORCID 0000-0003-4197-6264
Nicolas U GerberDepartment of Oncology, University Children's Hospital, Zurich, Switzerland.
Thomas TraunwieserDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Rolf-Dieter KortmannDepartment of Radiation Oncology, University of Leipzig, Leipzig, Germany.ORCID 0000-0002-8952-1819
Monika Warmuth-MetzInstitute of Diagnostic and Interventional Neuroradiology, University Hospital Wuerzburg, Wuerzburg, Germany.ORCID 0000-0002-3544-319X
Brigitte BisonDepartment of Neuroradiology, University Hospital Augsburg, Augsburg, Germany.
Ulrich-W ThomaleDepartment of Neurosurgery, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Juergen KraussDepartment for Neurosurgery, University Hospital Wuerzburg, Wuerzburg, Germany.
Torsten PietschInstitute of Neuropathology, Brain Tumor Reference Center of the German Society for Neuropathology and Neuroanatomy (DGNN), University of Bonn, DZNE German Center for Neurodegenerative Diseases, Bonn, Germany.ORCID 0000-0003-0763-6506
Steven C CliffordWolfson Childhood Cancer Research Centre, Newcastle University Centre for Cancer, Newcastle University, Newcastle Upon Tyne, UK.
Stefan M PfisterHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Dominik SturmHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Felix SahmHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.ORCID 0000-0001-5441-1962
Tanja TischlerDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Stefan RutkowskiDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0002-5446-9571

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurocognition can be severely affected in pediatric brain tumor survivors. We analyzed the association of cognitive functioning with radiotherapy dose, postoperative cerebellar mutism syndrome (pCMS), hydrocephalus, intraventricular methotrexate (MTX) application, tumor localization, and biology in pediatric survivors of a posterior fossa tumor.

methodsSubdomain-specific neurocognitive outcome data from 279 relapse-free survivors of the HIT-2000 trial (241 medulloblastoma and 38 infratentorial ependymoma) using the Neuropsychological Basic Diagnostic tool based on Cattell-Horn-Carroll's model for intelligence were analyzed.

resultsCognitive performance 5.14 years (mean; range = 1.52-13.02) after diagnosis was significantly below normal for all subtests. Processing speed and psychomotor abilities were most affected. Influencing factors were domain-specific: CSI-dose had a strong impact on most subtests. pCMS was associated with psychomotor abilities (β = -0.25 to -0.16) and processing speed (β = -0.32). Postoperative hydrocephalus correlated with crystallized intelligence (β = -0.20) and short-term memory (β = -0.15), age with crystallized intelligence (β = 0.15) and psychomotor abilities (β = -0.16 and β = -0.17). Scores for fluid intelligence (β = -0.23), short-term memory (β = -0.17) and visual processing (β = -0.25) declined, and scores for selective attention improved (β = 0.29) with time after diagnosis.

conclusionsThe dose of CSI was strongly associated with neurocognitive outcomes. Low psychomotor abilities and processing speed both in patients treated with and without CSI suggest a strong contribution of the tumor and its surgery on these functions. Future research therefore should analyze strategies to both reduce CSI dose and toxicity caused by other treatment modalities.

Indexed as

Infratentorial NeoplasmsMedulloblastomaAdolescentCancer SurvivorsChildChild, PreschoolCognition DisordersEpendymomaFemaleFollow-Up StudiesHumansHydrocephalusMaleMutismNeuropsychological TestsPrognosisependymomainfantmedulloblastomaneuropsychological late effectsquality of survival

Identifiers

PMID38835160
PMCPMC11534318

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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.