Quality of survival assessment in European childhood brain tumour trials, for children below the age of 5 years.


Journal

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
ISSN: 1532-2130
Titre abrégé: Eur J Paediatr Neurol
Pays: England
ID NLM: 9715169

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 14 04 2019
revised: 03 10 2019
accepted: 12 10 2019
pubmed: 23 11 2019
medline: 18 8 2020
entrez: 23 11 2019
Statut: ppublish

Résumé

The highest incidence rate of childhood brain tumours is in children below the age of five years, who are particularly vulnerable to the effects of treatments. The assessment of quality of survival (QoS) in multiple domains is essential to compare the outcomes for different tumour types and treatment regimens. The aim of this position statement is to present the domains of health and functioning to be assessed in children from birth to five years, to advance the collection of a common QoS data set in European brain tumour trials. The QoS group of the European Society of Paediatric Oncology (SIOP-E) Brain Tumour group conducted consensus discussions over a period of six years to establish domains of QoS that should be prioritised in clinical trials involving children under 5 years. The domains of health and functioning that were agreed to affect QoS included: medical outcomes (e.g. vision, hearing, mobility, endocrine), emotion, behaviour, adaptive behaviour, and cognitive functioning. As for children aged five years and older, a 'core plus' approach is suggested in which core assessments are recommended for all clinical trials. The core component for children from birth to three years includes indirect assessment which, in this age-group, requires proxy assessment by a parent, of cognitive, emotional and behaviour variables and both direct and indirect endocrine measures. For children from four years of age direct cognitive assessment is also recommended as 'core'. The 'plus' components enable the addition of assessments which can be selected by individual countries and/or by, age-, treatment-, tumour type- and tumour location-specific trials.

Identifiants

pubmed: 31753708
pii: S1090-3798(19)30391-5
doi: 10.1016/j.ejpn.2019.10.002
pii:
doi:

Types de publication

Guideline Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

59-67

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

J Limond (J)

Department of Psychology, University of Exeter, UK. Electronic address: j.limond@exeter.ac.uk.

S Thomas (S)

Department of Psychology and Neuropsychology, Nottingham University Hospitals NHS Trust, UK; Children's Brain Tumour Research Centre, University of Nottingham, UK.

K S Bull (KS)

Clinical and Experimental Sciences, University of Southampton, UK.

G Calaminus (G)

Pediatric Hematology and Oncology, University Childrens Hospital Bonn, Germany.

J Lemiere (J)

Pediatric Hemato-Oncology, UZLeuven, Leuven, Belgium.

T Traunwieser (T)

Swabian Children's Cancer Center, University Children's Hospital, Augsburg, Germany.

H M van Santen (HM)

Department of Pediatric Endocrinology, Wilhelmina Children's Hospital, UMCU, Utrecht, the Netherlands.

L Weiler (L)

Department of Pediatrics and Adolscent Medicine, General Hospital, Medical University of Vienna, Austria.

H A Spoudeas (HA)

Department of Neuroendocrinology, London Centre for Paediatric and Adolescent Endocrinology at Great Ormond Street and University College Hospitals, London, UK.

M Chevignard (M)

Rehabilitation Department, Outreach Team for Children and Adolescents with Acquired Brain Injury, Saint-Maurice Hospitals, 14 Rue du Val d'Osne, 94410 Saint-Maurice, France; Sorbonne Université, Laboratoire d'Imagerie Biomédicale, LIB, 75006 Paris, France.

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Classifications MeSH