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Acta Oncol. 2019 Oct 8:1-7. doi: 10.1080/0284186X.2019.1672892. [Epub ahead of print]

Neurologic disorders in long-term survivors of neuroblastoma - a population-based cohort study within the Adult Life after Childhood Cancer in Scandinavia (ALiCCS) research program.

Author information

1
Danish Cancer Society Research Center, Childhood Cancer Research Group , Copenhagen , Denmark.
2
Rigshospitalet, Department of Pediatric and Adolescent Medicine, Copenhagen University Hospital , Copenhagen , Denmark.
3
Unit of Statistics and Pharmacoepidemiology, Danish Cancer Society Research Center , Copenhagen , Denmark.
4
Department of Pediatric and Adolescent Medicine, Aarhus University Hospital , Aarhus , Denmark.
5
Department of Clinical Sciences, Lund University , Lund , Sweden.
6
Division of Paediatric Oncology and Haematology, Skane University Hospital , Lund , Sweden.
7
The Icelandic Cancer Registry , Reykjavik , Iceland.
8
Faculty of Medicine, University of Iceland , Reykjavik , Iceland.
9
The Finnish Cancer Registry , Helsinki , Finland.
10
Pediatric Oncology, National University Hospital of Iceland , Reykjavik , Iceland.
11
University of Helsinki Hospital for Children and Adolescents , Helsinki , Finland.
12
Department of Clinical Medicine, Faculty of Health, Aarhus University and University Hospital , Aarhus , Denmark.

Abstract

Background: Neuroblastoma is the commonest extracranial solid tumor of childhood, yet rare, and with poor survival before 1990, especially for high-risk disease; thus, information on late effects is sparse. With great advances in cancer treatment, survival has reached 80% in the Nordic countries. The aim of the study was to investigate the risk of developing neurologic disorders after neuroblastoma. Material and methods: Through population-based cancer registries of four Nordic countries we identified 654 5-year survivors of neuroblastoma (diagnosed 1959-2008) and 133,668 matched population comparisons. We grouped neurologic diagnoses from national hospital registries into 11 main diagnostic categories and 56 disease-specific sub-categories and calculated relative risks (RRs), absolute excess risks (AERs), cumulative incidence and mean cumulative count (MCC). Information on cancer treatment was available for 49% of survivors. Results: A hospital contact for a neurologic disorder was observed in 181 survivors 5 years or more from cancer diagnosis with 59 expected, yielding a RR of 3.1 (95% CI 2.7-3.6) and an AER of 16 per 1,000 person-years (95% CI 12-19). The most frequent disorders included epilepsy, paralytic syndromes, diseases of the eyes and ears and hearing loss. The cumulative incidence of any neurologic disorder was 31% in survivors 20 years after cancer diagnosis with a MCC of 0.5 unique diagnoses. All risks were highest in survivors of high-risk neuroblastoma. Conclusion: Neuroblastoma survivors represent a population with a high risk of developing neurologic disorders. Our results should contribute to improving health care planning and underscores the need for systematic follow-up care of this vulnerable group of survivors.

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