TY - JOUR
T1 - Overview of European standard clinical practice recommendations for multidiscplinary teams involved in the treatment of central nervous system tumours in children and adolescents – SIOPE Brain Tumour Group
AU - Otth, Maria
AU - Scheinemann, Katrin
AU - Ajithkumar, Thankamma
AU - Aquilina, Kristian
AU - Avula, Shivaram
AU - Gan, Hoong Wei
AU - Janssens, Geert O.
AU - Lemiere, Jurgen
AU - Morana, Giovanni
AU - Opocher, Enrico
AU - Pfister, Stefan M.
AU - Porro, Giorgio
AU - Sahm, Felix
AU - Thomale, Ulrich Wilhelm
AU - van Egmond-Ebbeling, Michelle
AU - van Santen, Hanneke M.
AU - Pizer, Barry
AU - Rutkowski, Stefan
N1 - Publisher Copyright:
© 2024
PY - 2024/6
Y1 - 2024/6
N2 - Tumours of the central nervous system (CNS) represent the most common group of solid tumours in children and adolescents up to the age of 18 years. They comprise several biological entities, subgroups, and subtypes. These subtypes and additional factors, including age at diagnosis, location, stage, or genetic characteristics of the tumours result in a very heterogeneous spectrum of treatment-relevant strata for risk-adapted multimodal treatment recommendations, clinical courses, and long-term outcomes. Multidisciplinary teams with highly experienced members are needed to treat these children and adolescents to achieve the best possible outcome in the short and long-term. This is particularly important for the new CNS tumour entities with no established standard of care. On behalf of the Brain Tumour Group of the European Society for Paediatric Oncology, we summarize the key statements of the involved disciplines that need to cooperate in the diagnosis and risk-adapted treatment of children with CNS tumours: neuroradiology, neurosurgery, neuropathology, radiotherapy, endocrinology, neuro-ophthalmology, and quality of survival professionals, covering what should be considered standard clinical practice for diagnostic assessments, treatment modalities, and follow-up of children with CNS-tumours.
AB - Tumours of the central nervous system (CNS) represent the most common group of solid tumours in children and adolescents up to the age of 18 years. They comprise several biological entities, subgroups, and subtypes. These subtypes and additional factors, including age at diagnosis, location, stage, or genetic characteristics of the tumours result in a very heterogeneous spectrum of treatment-relevant strata for risk-adapted multimodal treatment recommendations, clinical courses, and long-term outcomes. Multidisciplinary teams with highly experienced members are needed to treat these children and adolescents to achieve the best possible outcome in the short and long-term. This is particularly important for the new CNS tumour entities with no established standard of care. On behalf of the Brain Tumour Group of the European Society for Paediatric Oncology, we summarize the key statements of the involved disciplines that need to cooperate in the diagnosis and risk-adapted treatment of children with CNS tumours: neuroradiology, neurosurgery, neuropathology, radiotherapy, endocrinology, neuro-ophthalmology, and quality of survival professionals, covering what should be considered standard clinical practice for diagnostic assessments, treatment modalities, and follow-up of children with CNS-tumours.
KW - Central nervous system tumour
KW - child
KW - endocrinology
KW - neuro-ophthalmology
KW - neuropathology
KW - neuroradiology
KW - neurosurgery
KW - quality of survival
KW - radiotherapy
KW - recommendation
UR - http://www.scopus.com/inward/record.url?scp=85194186524&partnerID=8YFLogxK
U2 - 10.1016/j.ejcped.2024.100166
DO - 10.1016/j.ejcped.2024.100166
M3 - Article
AN - SCOPUS:85194186524
SN - 2772-610X
VL - 3
JO - EJC Paediatric Oncology
JF - EJC Paediatric Oncology
M1 - 100166
ER -