TY - JOUR
T1 - Intraoperative radiation therapy for high-risk pediatric neuroblastoma
AU - Haas-Kogan, Daphne A.
AU - Fisch, Benjamin M.
AU - Wara, William M.
AU - Swift, Patrick S.
AU - Farmer, Diana L.
AU - Harrison, Michael R.
AU - Albanese, Craig
AU - Weinberg, Vivian
AU - Matthay, Katherine K.
N1 - Funding Information:
This work was supported in part by NIH grant #M01RR01271 and an award from the American Society of Clinical Oncology (D.A.H.-K.) as well as the Kasle & Tkalcevic Neuroblastoma Research Fund (K.K.M.).
PY - 2000/7/1
Y1 - 2000/7/1
N2 - Purpose: To evaluate the efficacy of intraoperative radiation therapy (IORT) in the treatment of high-risk pediatric neuroblastoma.Methods and Materials: Between 1986 and 1998, 23 children received IORT for pediatric neuroblastoma. Electron beam energies ranged from 4 MeV to 16 MeV and median dose was 10 Gy (7-16 Gy).Results: Twenty-one of 23 patients were classified as high-risk. A gross total resection (GTR) was achieved in 18 patients, of whom 6 experienced disease recurrence, 2 of which included a locoregional relapse as a component of failure. Fourteen of 18 patients receiving IORT after a GTR are disease-free survivors. A second subset of 5 patients had a subtotal resection (STR), with gross residual disease remaining after surgery. All 5 patients recurred locally, and all died of their disease. IORT was extremely well-tolerated in our cohort. Surgical resection and IORT resulted in the narrowing of the abdominal aorta and an atrophic kidney in 1 patient.Conclusions: For high-risk neuroblastoma patients, IORT as the only radiotherapy to the primary, produced excellent local control after a GTR. However, IORT as the sole radiotherapy to the primary was inadequate for patients with extensive adenopathy or an STR. In this setting, we are exploring the use of IORT as a boost in conjunction with external beam radiation therapy. Copyright (C) 2000 Elsevier Science Inc.
AB - Purpose: To evaluate the efficacy of intraoperative radiation therapy (IORT) in the treatment of high-risk pediatric neuroblastoma.Methods and Materials: Between 1986 and 1998, 23 children received IORT for pediatric neuroblastoma. Electron beam energies ranged from 4 MeV to 16 MeV and median dose was 10 Gy (7-16 Gy).Results: Twenty-one of 23 patients were classified as high-risk. A gross total resection (GTR) was achieved in 18 patients, of whom 6 experienced disease recurrence, 2 of which included a locoregional relapse as a component of failure. Fourteen of 18 patients receiving IORT after a GTR are disease-free survivors. A second subset of 5 patients had a subtotal resection (STR), with gross residual disease remaining after surgery. All 5 patients recurred locally, and all died of their disease. IORT was extremely well-tolerated in our cohort. Surgical resection and IORT resulted in the narrowing of the abdominal aorta and an atrophic kidney in 1 patient.Conclusions: For high-risk neuroblastoma patients, IORT as the only radiotherapy to the primary, produced excellent local control after a GTR. However, IORT as the sole radiotherapy to the primary was inadequate for patients with extensive adenopathy or an STR. In this setting, we are exploring the use of IORT as a boost in conjunction with external beam radiation therapy. Copyright (C) 2000 Elsevier Science Inc.
KW - Intraoperative radiation
KW - Neuroblastoma
KW - Pediatric
UR - http://www.scopus.com/inward/record.url?scp=0034237688&partnerID=8YFLogxK
U2 - 10.1016/S0360-3016(00)00432-6
DO - 10.1016/S0360-3016(00)00432-6
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C2 - 10863069
AN - SCOPUS:0034237688
VL - 47
SP - 985
EP - 992
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
SN - 0360-3016
IS - 4
ER -