Hospital admission for neurologic disorders among 5-year survivors of noncentral nervous system tumors in childhood: A cohort study within the Adult Life after Childhood Cancer in Scandinavia study.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 02 2020
Historique:
received: 27 11 2018
revised: 27 03 2019
accepted: 02 04 2019
pubmed: 14 4 2019
medline: 12 2 2020
entrez: 14 4 2019
Statut: ppublish

Résumé

Large, comprehensive studies of the risk for neurologic disorders among long-term survivors of noncentral nervous system (CNS) childhood cancers are lacking. Thus, the aim of our study was to assess the lifetime risk of Nordic non-CNS childhood cancer survivors for neurologic disorders. We identified 15,967 5-year survivors of non-CNS childhood cancer diagnosed in Denmark, Iceland, Finland and Sweden in 1943-2008, and 151,118 matched population comparison subjects. In-patient discharge diagnoses of neurologic disorders were used to calculate relative risks (RRs) and absolute excess risks (AERs). A neurologic disorder was diagnosed in 755 of the survivors while 370 were expected, yielding a RR of 2.0 (95% confidence interval (CI) 1.9-2.2). The highest risks were found among survivors of neuroblastoma (4.1; 95% CI 3.2-5.3) and leukemia (2.8; 95% CI 2.4-3.2). The AER decreased from 331 (278-383) excess neurologic disorders per 100,000 person-years 5-9 years after diagnosis to 82 (46-118) ≥ 20 years after diagnosis. Epilepsy was the most common diagnosis (n = 229, 1.4% of all survivors), and significantly increased risks were seen among survivors of eight out of 12 types of childhood cancer. Survivors of neuroblastoma had remarkably high risks (RR ≥ 10) for hospitalization for paralytic syndromes and hydrocephalus, while survivors of leukemia had additional high risks for dementia and encephalopathy. In conclusion, survivors of non-CNS childhood cancer are at high risk for neurologic disorders, especially within the first decade after diagnosis. Therefore, intensive follow-up to identify those who require close management is needed.

Identifiants

pubmed: 30980681
doi: 10.1002/ijc.32341
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

819-828

Informations de copyright

© 2019 UICC.

Références

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Auteurs

Line Kenborg (L)

Childhood Cancer Research Group, Danish Cancer Society Research Center, Copenhagen, Denmark.

Karen M Linnet (KM)

Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.

Sofie de Fine Licht (S)

Childhood Cancer Research Group, Danish Cancer Society Research Center, Copenhagen, Denmark.

Andrea Bautz (A)

Childhood Cancer Research Group, Danish Cancer Society Research Center, Copenhagen, Denmark.

Anna S Holmqvist (AS)

Department of Clinical Sciences, Lund University, Lund, Sweden.
Pediatric Oncology and Hematology, Skåne University Hospital, Lund, Sweden.

Laufey Tryggvadottir (L)

Icelandic Cancer Registry, Reykjavik, Iceland.
Faculty of Medicine, University of Iceland, Reykjavik, Iceland.

Laura M Madanat-Harjuoja (LM)

Finnish Cancer Registry, Helsinki, Finland.

Marilyn Stovall (M)

Department of Radiation Physics, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

Carsten Heilmann (C)

Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.

Vanna Albieri (V)

Unit of Statistics and Pharmacoepidemiology, Danish Cancer Society Research Center, Copenhagen, Denmark.

Henrik Hasle (H)

Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.

Jeanette F Winther (JF)

Childhood Cancer Research Group, Danish Cancer Society Research Center, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health, Aarhus University Hospital, Aarhus, Denmark.

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