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This phase II trial studies the side effects of hypofractionated radiation therapy in treating patients with soft tissue sarcomas prior to surgery. Hypofractionated radiation therapy delivers higher doses of radiation therapy over a shorter period of time and may kill more tumor cells and have fewer side effects.
PRIMARY OBJCETIVES: I. Grade \>= 2 radiation morbidity (subcutaneous tissue fibrosis, joint stiffness, or edema) at 2 years. SECONDARY OBJECTIVES: I. Evaluate local control, regional control, distant metastasis, progression free survival, and overall survival. II. Evaluate the functional outcomes as assessed using the musculoskeletal tumor rating scale (MSTS) and the Toronto Extremity Salvage Score (TESS). III. Collect germ-line deoxyribonucleic acid (DNA) and nucleic acids from cancer patients to further investigate the association and identify new germ-line mutations that impact cancer predisposition. IV. Investigate the role of germ-line mutations in predicting cancer outcome and response to therapy. OUTLINE: Patients undergo hypofractionated radiation therapy on Monday-Friday for 5 days. Beginning 2-12 weeks after completion of radiation therapy, patients undergo surgery. After completion of study treatment, patients are followed up at 3 months and then every 6 months for 5 years.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
UCLA / Jonsson Comprehensive Cancer Center
Los Angeles, California, United States
Start Date
February 3, 2016
Primary Completion Date
February 3, 2027
Completion Date
February 3, 2028
Last Updated
March 10, 2026
51
ESTIMATED participants
Conventional Surgery
PROCEDURE
Hypofractionated Radiation Therapy
RADIATION
Laboratory Biomarker Analysis
OTHER
Questionnaire Administration
OTHER
Lead Sponsor
Jonsson Comprehensive Cancer Center
Collaborators
NCT01552434
NCT01462630
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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