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Journal ArticleDOI

International variations in the incidence of neuroblastoma.

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TLDR
Incidence was generally higher in regions and among ethnic groups enjoying a higher standard of living, though previous studies within single countries had suggested that neuroblastoma is more common among less affluent groups.
Abstract
The International Agency for Research on Cancer has coordinated a worldwide study of childhood cancer incidence, with data from over 50 countries. We present here the results for neuroblastoma. In predominantly white Caucasian populations the age-standardized rate was 7-12 per million, and 6-10% of all childhood cancers were neuroblastomas. Rates were highest in the first year of life (25-50 per million, 30% of total neuroblastoma incidence), and decreased with age to 15-20 per million (50% of the total) at age 1-4, 2-4 per million (15%) at 5-9 and 1-1.5 per million (5%) at 10-14. In the United States, black children had an incidence of 8.5 per million compared with 11.5 among Whites; Blacks tended to be older than Whites at diagnosis. The highest rate in Africa was in Bulawayo, Zimbabwe (8.0 per million) and the lowest in West Nile, Uganda, with no cases registered. Incidence in Israel was similar to that in many white populations, with Jews having a particularly high rate. In other parts of West Asia neuroblastoma had a low relative frequency, suggesting that incidence is low. Rates were also low throughout much of southern and eastern Asia, including India and China. Incidence in Japan was somewhat higher, though less than in Western countries, with the deficit most pronounced in the first year of life; these data relate to the period before mass screening of infants for neuroblastoma in the regions concerned. Incidence was generally higher in regions and among ethnic groups enjoying a higher standard of living, though previous studies within single countries had suggested that neuroblastoma is more common among less affluent groups. Blacks in Africa and the United States may have a weaker genetic predisposition to neuroblastoma, but some of the deficit in many developing countries is likely to be due to under-diagnosis.

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Neuroblastoma: Biology, Prognosis, and Treatment

TL;DR: This article summarizes the understanding of neuroblastoma biology and prognostic features and discusses their impact on current and proposed risk stratification schemas, risk-based therapeutic approaches, and the development of novel therapies for patients at high risk for failure.
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Neuroblastoma

TL;DR: Neuroblastoma is a type of cancer that most often affects children and can spread to other parts of the body such as the bones, liver, or skin.
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Neuroblastoma: Paradigm for Precision Medicine

TL;DR: Current clinical trials have continued to reduce therapy for patients with non-high-risk NB, including the most favorable subsets who are often followed with observation approaches, and high-risk patients are treated aggressively with chemotherapy, radiation, surgery, and myeloablative and immunotherapies.
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Geographic and ethnic variations in the incidence of childhood cancer

TL;DR: The total incidence of childhood cancer varies rather little between different regions of the world, with cumulative risk to age 15 nearly always in the range 1.0-2.5 per thousand; the incidence of Kaposi's sarcoma has risen substantially in parts of Africa severely affected by the AIDS epidemic.
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Overview and recent advances in the treatment of neuroblastoma

TL;DR: The identification of newer tumor targets and of novel cell-mediated immunotherapy agents may lead to novel therapeutic approaches, and clinical trials for regimens designed to target individual genetic aberrations in tumors are underway.
References
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Journal ArticleDOI

The international incidence of childhood cancer

TL;DR: Variations in the risk of those tumours between different countries and different ethnic groups provide important information on the relative importance of environmental and genetic factors in their aetiology.
Journal ArticleDOI

A classification scheme for childhood cancer.

TL;DR: There is a great need for standardization in the classification of childhood cancers and it is proposed that the scheme described below be used for presentation of incidence data for results of aetiologicaf and other related studies of cancer in children.
Journal Article

Medical and drug risk factors associated with neuroblastoma: a case-control study.

TL;DR: A matched case-control study of prenatal risk factors for neuroblastoma was conducted, including 104 cases diagnosed over the period 1970-79 in the Greater Delaware Valley, and significantly elevated odds ratios were associated with maternal use of a neurally active drug during pregnancy.
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Familial neuroblastoma: case reports, literature review, and etiologic considerations

TL;DR: The phenomenon of familial Neuroblastoma is discussed in the context of case reports describing disseminated neuroblastoma in two of three half‐brothers who share a common unaffected mother and who each have a different father.
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Childhood cancer and ethnic group in Britain: a United Kingdom children's Cancer Study Group (UKCCSG) study.

TL;DR: The results suggest that the incidence of childhood acute lymphoblastic leukaemia is associated with environmental determinants in the country of residence which are most likely to relate to lifestyle factors.
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