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Int J Radiat Oncol Biol Phys ; 83(1): 317-26, 2012 May 01.
Article in English | MEDLINE | ID: mdl-22104361

ABSTRACT

PURPOSE: Desmoplastic small round cell tumor (DSCRT) is an uncommon pediatric tumor with a poor prognosis. Aggressive multimodality therapy is the current treatment approach; however. treatment toxicity is of concern. We report our results with whole abdominopelvic intensity-modulated radiation therapy (WAP-IMRT) as a component of multimodality therapy for DSCRT at a single institution. MATERIALS/METHODS: Medical records of all patients with DSCRT who received WAP-IMRT as part of definitive treatment at MD Anderson (2006-2010) were identified and reviewed. RESULTS: Eight patients with DSRCT received WAP-IMRT with a median follow-up of 15.2 months. All patients received multiple courses of chemotherapy followed by surgical debulking of intra-abdominal disease; seven also had intraoperative hyperthermic cisplatin. WAP-IMRT was delivered to a total dose of 30 Gy postoperatively; four patients received a simultaneous boost (6-10 Gy) to sites of gross residual disease. Seven patients received concurrent chemotherapy during WAP-IMRT. No Radiation Therapy Oncology Group Grade 4 nausea, vomiting, or diarrhea occurred during RT. Red-cell transfusions were given to two patients to maintain hemoglobin levels >10 g/dL. Grade 4 cytopenia requiring growth factor support occurred in only one patient; no other significant cytopenias were noted. WAP-IMRT resulted in 25% lower radiation doses to the lumbosacral vertebral bodies and pelvic bones than conventional RT plans. The median time to local or distant failure after WAP-IMRT was 8.73 months in seven patients. One patient who had completed RT 20 months before the last follow-up remains alive without evidence of disease. Five patients (63%) experienced treatment failure in the abdomen. Distant failure occurred in three patients (37.5%). CONCLUSIONS: WAP-IMRT with concurrent radiosensitizing chemotherapy was well tolerated after aggressive surgery for DSCRT. Enhanced bone sparing with IMRT probably accounts for the low hematologic toxicity (vs. conventional WAP-RT). This modality should be considered as an additional local-regional control option for DSRCT.


Subject(s)
Abdominal Neoplasms/radiotherapy , Desmoplastic Small Round Cell Tumor/radiotherapy , Radiotherapy, Intensity-Modulated/methods , Abdominal Neoplasms/drug therapy , Abdominal Neoplasms/surgery , Adolescent , Antibodies, Monoclonal, Humanized/administration & dosage , Antineoplastic Agents/therapeutic use , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bevacizumab , Camptothecin/administration & dosage , Camptothecin/analogs & derivatives , Child , Child, Preschool , Cisplatin/therapeutic use , Combined Modality Therapy/methods , Cyclophosphamide/administration & dosage , Dacarbazine/administration & dosage , Dacarbazine/analogs & derivatives , Desmoplastic Small Round Cell Tumor/drug therapy , Desmoplastic Small Round Cell Tumor/surgery , Erythrocyte Transfusion/methods , Feasibility Studies , Humans , Hyperthermia, Induced/methods , Interferons/administration & dosage , Irinotecan , Liver Neoplasms/radiotherapy , Liver Neoplasms/secondary , Male , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/radiotherapy , Pelvic Neoplasms/surgery , Peritoneal Neoplasms/radiotherapy , Peritoneal Neoplasms/secondary , Peritoneal Neoplasms/surgery , Radiation-Sensitizing Agents/therapeutic use , Radiotherapy Dosage , Radiotherapy Planning, Computer-Assisted/methods , Radiotherapy, Intensity-Modulated/adverse effects , Retrospective Studies , Temozolomide , Thrombocytopenia/etiology , Vinblastine/administration & dosage , Vinblastine/analogs & derivatives , Vinorelbine , Young Adult
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