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SARC018: A SARC PILOT MULTICENTER STUDY OF PREOPERATIVE RADIATION AND SURGERY IN PATIENTS WITH HIGH- RISK DESMOID TUMORS Robert S. Benjamin, M.D.
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Objectives The trial ’ s primary objectives are to determine feasibility of performing a multicenter study of radiation therapy through SARC and to determine overall progression-free survival from start of treatment in these patients.
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Background Patients with desmoid fibromatosis and 45F beta catenin mutation (28% in our series) who underwent surgical resection as initial therapy at our institution have a 45% 3- or 5-year recurrence-free survival compared with about 80% for those with 41A mutation or no detectable mutation.
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Background (continued) Radiation therapy has been effective in the treatment of desmoid patients with a similar degree of local control as surgery. Of the 7 patients received radiotherapy in combination with surgery, 2 (28%) experienced tumor recurrence within the follow up period, in contrast with 21/27 patients (77%) who have not been treated with radiation.
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Screening Slides for diagnosis and unstained slides or blocks for DNA extraction should be sent to Dr. Dina Lev at M.D. Anderson. Patients with 45F beta catenin mutation would be considered for the protocol.
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Eligibility Desmoid tumor with 45 F beta catenin mutation and no FAP mutation. Tumor must be Resectable <25 cm in largest dimension Location such that radiation can be delivered with acceptable normal tissue toxicity In an region that has not been previously irradiated
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Pretreatment Evaluation MRI with and without contrast should be obtained on each patient. The post-contrast T1 image will be used for radiation planning.
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Radiation Therapy Either 3D conformal radiation therapy or intensity modulated radiation therapy or electron radiotherapy may be utilized as deemed appropriate. A prescription dose of 50 Gy in 25 daily fractions will be prescribed.
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Surgery Wide resection of the tumor will be performed 4-8 weeks following completion of radiation therapy.
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Follow-up In addition to physical examination, CT, MRI, or Ultrasound will be performed on the following schedule: Years 1-3: Every 4 months Years 4-5: Every 6 months Years 6-10: Every 12 months
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Radiation Therapy Quality Assurance Radiation treatment planning records will be sent to Dr. Ashleigh Guadagnolo at M.D. Anderson for review. If any portion of the gross target volume (GTV) receives <50 Gy, that is a major protocol violation. If any portion of the clinical target volume (CTV) receives <50 Gy, that is a minor protocol violation.
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Statistical Considerations This is a pilot study to determine if a larger study could be performed and is of clinical interest. Major protocol violations should not exceed 3 patients (10%). A median progression-free survival of >4.5 years would be of interest, while a median progression-free survival of 2.6 years would not warrant further study.
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