Journal of Clinical Oncology, Vol 16, 3761-3767, Copyright © 1998 by American Society of Clinical Oncology
Secondary brain tumors in children treated for acute lymphoblastic leukemia at St Jude Children's Research Hospital
AW Walter, ML Hancock, CH Pui, MM Hudson, JS Ochs, GK Rivera, CB Pratt, JM Boyett and LE Kun
Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38105, USA. andrew.walter@stjude.org
PURPOSE: To evaluate the incidence of and potential risk factors for second
malignant neoplasms of the brain following treatment for childhood acute
lymphoblastic leukemia (ALL). PATIENTS AND METHODS: The study population
consisted of 1,612 consecutively enrolled protocol patients treated on
sequential institutional protocols for newly diagnosed ALL at St Jude
Children's Research Hospital (SJCRH) between 1967 and 1988. The median
follow-up duration is 15.9 years (range, 5.5 to 29.9 y). RESULTS: The
cumulative incidence of brain tumors at 20 years is 1.39% (95% confidence
interval [CI], 0.63% to 2.15%). Twenty- two brain tumors (10 high-grade
gliomas, one low-grade glioma, and 11 meningiomas) were diagnosed among 21
patients after a median latency of 12.6 years (high-grade gliomas, 9.1
years; meningiomas, 19 years). Tumor type was linked to outcome, with
patients who developed high- grade tumors doing poorly and those who
developed low-grade tumors doing well. Risk factors for developing any
secondary brain tumor included the presence of CNS leukemia at diagnosis,
treatment on Total X therapy, and the use of cranial irradiation, which was
dose- dependent. Age less than 6 years was associated with an increased
risk of developing a high-grade glioma. CONCLUSION: This single-institution
study, with a high rate of long-term data capture, demonstrated that brain
tumors are a rare, late complication of therapy for ALL. We report many
more low-grade tumors than others probably because of exhaustive long-term
follow-up evaluation. The importance of limiting cranial radiation is
underscored by the dose-dependent tumorigenic effect of radiation therapy
seen in this study.
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