Volume 64, Issue 4 , Pages 1038-1043, 15 March 2006
Impact of radiotherapy for pediatric CNS atypical teratoid/rhabdoid tumor (single institute experience)
Purpose: To assess outcomes and prognostic factors in radiotherapy of pediatric central nervous system atypical teratoid/rhabdoid tumor (AT/RT).
Methods and Materials: Seventeen patients with central nervous system AT/RT were retrospectively reviewed after curative radiotherapy as primary or adjuvant therapy between January 1990 and December 2003. Overall and failure-free survival rates were calculated using the Kaplan–Meier method. The log–rank method was used to compare the effects of dosage (>50 Gy or ≤50 Gy) and treatment duration (>45 days or ≤45 days). Multivariate analysis was performed for prognostic factors.
Results: Median overall survival and failure-free survival were 17 and 11 months, respectively. The 3 longest-surviving patients were older, underwent gross tumor removal, and completed both craniospinal and focal boost irradiation. Multivariate analysis revealed a significant relationship between the following: overall survival and performance status (p = 0.019), failure-free survival and total irradiation dose (p = 0.037), time interval between surgery and radiotherapy initiation (p = 0.031), and time interval between surgery and radiotherapy end point (p = 0.047).
Conclusion: Radiotherapy is crucial in the treatment of AT/RT. We recommend initiating radiotherapy immediately postoperatively and before systemic chemotherapy in pediatric patients ≥3 years of age.
Keywords: Atypical teratoid/rhabdoid tumor , Brain neoplasm , Radiotherapy , Craniospinal irradiation , Combined modality therapy
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The authors are grateful for financial support received for this study via Grant No. VGH94–139.
PII: S0360-3016(05)02735-5
doi:10.1016/j.ijrobp.2005.10.001
© 2006 Elsevier Inc. All rights reserved.
Volume 64, Issue 4 , Pages 1038-1043, 15 March 2006
