Evidence map›Paper›PMID 39030984›Full record

ArticleAnnals of clinical and translational neurology2024

CSF biomarkers of neurotoxicity in childhood cancer survivors after cranial radiotherapy or surgery.

Erik Fernström, Marianne Jarfelt, Malin Blomstrand, Birgitta Lannering, Markus Axelsson, Pontus Wasling, Thomas Björk-Eriksson, Henrik Zetterberg, Marie Kalm

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Erik FernströmDepartment of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0000-0002-0769-4602
Marianne JarfeltDepartment of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.
Malin BlomstrandDepartment of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.
Birgitta LanneringDepartment of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Markus AxelssonDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Pontus WaslingDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Thomas Björk-ErikssonDepartment of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Marie KalmDepartment of Pharmacology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.

Funding

Alzheimer Drug Discovery Foundation (ADDF), USA 201809-2016862Alzheimer's Association ADSF-21-831376-CAlzheimer's Association ADSF-21-831377-CAlzheimer's Association ADSF-21-831381-CAlzheimer's Association ADSF-24-1284328-CCure Alzheimer's FundErling-Persson Family FoundationEU Joint Programme - Neurodegenerative Disease Research JPND2021-00694European Union Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement (MIRIADE) 860197European Union Horizon Europe Research and Innovation Programme 101053962Familjen Rönströms StiftelseFrimurare Barnhus Foundations of GothenburgHjärnfonden, Sweden FO2022-0270Jubileumskliniken Anti-cancer Research FundLions Cancer Fund of Western SwedenNational Institute for Health and Care Research, University College London Hospitals Biomedical Research CentreOlav Thon FoundationStiftelsen för Gamla TjänarinnorSwedish Childhood Cancer FoundationSwedish Research Council 2019-02397Swedish Research Council 2022-01018Swedish Research Council 2023-00356Swedish Society of MedicineSwedish State under the ALF-Agreement ALFGBG-71320Swedish State under the ALF-Agreement ALFGBG-774991Swedish State under the ALF-Agreement ALFGBG-819811Swedish State under the ALF-Agreement ALFGBG-875691The Bluefield ProjectUK Dementia Research Institute at UCL UKDRI-1003
6 · The paper itself

Abstract

objectiveTreatment of pediatric brain tumors is associated with potential long-term cognitive sequelae. Patients treated with craniospinal irradiation for posterior fossa tumors are at high risk. New biomarkers that could help to differentiate treatment effects from other causes of cognitive dysfunction would be valuable in tailoring optimal survivorship care. Biomarkers that reflect biological mechanisms behind treatment-associated cognitive decline would also be important in the evaluation of future treatment regimens for pediatric brain or skull base tumors.

methodsIn this biomarker-finding study, 10 adult survivors of pediatric medulloblastoma, skull base tumors, and posterior fossa low-grade glioma underwent study specific lumbar puncture at a minimum of 17 years following treatment. We analyzed cerebrospinal fluid biomarkers reflecting neuron and astrocyte integrity, amyloid metabolism, inflammation, extracellular matrix, synaptic integrity, and blood-brain barrier function. The values were compared with biomarker levels in healthy controls of comparable age.

resultsBiomarkers reflecting neuronal injury (neurofilament light chain protein), astrocyte injury or activation (glial fibrillary acidic protein) as well as inflammation (YKL-40) were significantly elevated in cancer survivors compared to controls. Biomarkers reflecting amyloid metabolism showed a pattern of decrease in patients treated for medulloblastoma.

interpretationThe results suggest a potential chronic low-grade neurodegeneration and astrocyte activation in patients treated for pediatric brain or skull base tumors. Protein biomarkers of CNS disease could potentially be used to increase our understanding of the contribution from different tumor treatments with regard to long-term symptoms in cancer patients.

Indexed as

BiomarkersCancer SurvivorsMedulloblastomaAdolescentAdultBrain NeoplasmsCerebellar NeoplasmsChildCranial IrradiationFemaleGlial Fibrillary Acidic ProteinGliomaHumansInfratentorial NeoplasmsMaleNeurofilament ProteinsBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament Proteins

Identifiers

PMID39030984
PMCPMC11537133

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.