Intraoperative radiotherapy in the multidisciplinary treatment of bone sarcomas in children and adolescents
Calvo F.A., Ortiz de Urbina D., Sierrasesúmaga L., Abuchaibe O., Azinovic I., Antillon F., Santos M., Cañadell J.
Department of Radiation Oncology, Clínica Universitaria de Navarra, Facultad de Medicina, Spain
Magazine: Medical and Pediatric Oncology
Date: Jun 1, 1991Pediatría [SP]
From September 1984 to December 1989, 38 patients of pediatric age with localized bone sarcomas received intraoperative radiotherapy (IORT) as part of a multidisciplinary treatment program. The age ranged from 6 to 21 years.
The tumor histologies were 22 osteosarcomas and 16 Ewing's sarcomas. Thirty-four had initial primary disease (90%) and 4 were treated for local recurrence (10%). IORT was used on 32 untreated patients and in 6 previously treated with external beam radiotherapy (EBR). The IORT field included the surgically exposed tumor bed area. Single radiation doses ranging from 10 to 20 Gy were delivered, using 6-20 MeV electron beams. The median follow-up time for the entire group is 25 months (2-65+ months). The projected 5-year disease-free and overall survival rates are 65% and 69%, respectively. One patient developed a local recurrence in each histological group: one chondroblastic osteosarcoma and one cervical Ewing's sarcoma. Six patients died from metastatic progression: 3 initially recurrent tumors and three primary disease cases.
Severe neuropathy and soft tissue necrosis were seen in some patients as IORT related complications. IORT is a feasible technique to be integrated in multidisciplinary programs that may promote local control in pediatric and adolescent patients with bone sarcomas. Peripheral nerves are dose-limiting tissue structures for IORT.
CITATION Med Pediatr Oncol. 1991;19(6):478-85
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