Mortality From Second Tumors Among Long-Term Survivors of Retinoblastoma

Background: Children diagnosed with retinoblastoma, a rare cancer of the eye, tend to develop and die of second primary cancers in childhood and adolescence, but few investigations have followed patients into adulthood. Retinoblastoma is frequently caused by inherited mutations of the RB1 tumor supp...

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Veröffentlicht in:	JNCI : Journal of the National Cancer Institute 1993-07, Vol.85 (14), p.1121-1128
Hauptverfasser:	Eng, Charis, Li, Frederick P., Abramson, David H., Ellsworth, Robert M., Wong, F. Lennie, Goldman, Marlene B., Seddon, Johanna, Tarbell, Nancy, Boice, John D.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Biological and medical sciences Cancer Child Child, Preschool Children & youth Epidemiology Eye Neoplasms - genetics Eye Neoplasms - therapy Female Humans Infant Male Medical sciences Middle Aged Mortality Mutation Neoplasms, Radiation-Induced - mortality Neoplasms, Second Primary - etiology Neoplasms, Second Primary - genetics Neoplasms, Second Primary - mortality Radiotherapy - adverse effects Retina Retinoblastoma - genetics Retinoblastoma - therapy Retrospective Studies Risk Factors Surveys and Questionnaires Tumors United States - epidemiology
Online-Zugang:	Volltext
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