Reporting Incidences of Neuroblastoma in Various Resource Settings.


Journal

JCO global oncology
ISSN: 2687-8941
Titre abrégé: JCO Glob Oncol
Pays: United States
ID NLM: 101760170

Informations de publication

Date de publication:
06 2021
Historique:
entrez: 17 6 2021
pubmed: 18 6 2021
medline: 6 8 2021
Statut: ppublish

Résumé

The incidences of neuroblastoma (NB) differ significantly between various resource settings because of varying quality of cancer registries and underdiagnoses. This study aimed to evaluate current regional variations as reported by international cancer registries and the theoretical and reported differences in international NB incidences and to evaluate South Africa (SA) as a case for variable reporting. A comprehensive literature review on registries reporting on NB was performed to construct incidence tables. The SEER Program incidence of 10.5/million children was used to calculate the expected number of NB cases for each country. Registry data of NB cases between 2000 and 2016 were requested from The South African National Cancer registry (SA-NCR) and the South African Children's Tumour Registry (SACTR) for comparison and to perform a probabilistic linkage study. Internationally, incidences varied between -97.1% and +80% compared with the SEER program. SA under-reported NB cases by an estimated 74.2%. Between 2000 and 2016, the SA-NCR reported between 23 and 51 cases/year, whereas the SACTR reported between 18 and 57 cases/year for the same period. The incidence reported by the SA-NCR varied between 1.5 and 2.8/million children under 15-year per year, whereas the SACTR reported 1.74-2.6 cases/million children. Both registries reported incidences less than high-income country. A probabilistic record linkage of the two registries resulted in a combined incidence of 2.9 cases/million children. As with most low- and middle-income countries, SA has either a lower incidence or underdiagnoses of NB cases. The reasons for under-reporting are not clear, but can be due to undiagnosed NB cases with spontaneous regression, missed possible cases because of lack of autopsies, and diagnosed cases not recorded in registries.

Identifiants

pubmed: 34138644
doi: 10.1200/GO.21.00054
pmc: PMC8457875
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

947-964

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Auteurs

Jaques van Heerden (J)

Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Paediatric Haematology and Oncology, Department of Paediatrics Antwerp University Hospital, Antwerp, Belgium.

Natasha Abraham (N)

National Cancer Registry, National Health Laboratory Service, Johannesburg, South Africa.

Judy Schoeman (J)

Paediatric Haematology and Oncology, Department of Paediatrics University of Pretoria, Steve Biko Academic Hospital, Pretoria, South Africa.
South African Children's Tumour Registry, Pretoria, South Africa.

David Reynders (D)

Paediatric Haematology and Oncology, Department of Paediatrics University of Pretoria, Steve Biko Academic Hospital, Pretoria, South Africa.
South African Children's Tumour Registry, Pretoria, South Africa.

Elvira Singh (E)

National Cancer Registry, National Health Laboratory Service, Johannesburg, South Africa.
School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.

Mariana Kruger (M)

Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

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