期刊
JOURNAL OF PEDIATRICS
卷 144, 期 5, 页码 666-668出版社
MOSBY-ELSEVIER
DOI: 10.1016/j.jpeds.2004.02.026
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资金
- NCI NIH HHS [U10 CA24507, U10 CA98413-01] Funding Source: Medline
We identified all children enrolled in the Intergroup Rhabdomyosarcoma Study Group-IV with neurofibromatosis type I (NF1) and rhabdomyosarcoma. Among 1025 eligible patients, 5 (0.5%) had NF1. Three children had relapses, two of whom died of progressive disease. Patients with NF1 and rhabdomyosarcoma should be treated with intensive contemporary therapy protocols.
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