This clinical trial studies how well whole breast radiation therapy with simultaneous integrated boost works for patients with early-stage breast cancer or ductal carcinoma in situ. Breast surgery along with radiation therapy is the standard of care for most patients and provides a reduction in cancer that comes back after a period of improvement (recurrence). Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Standard treatment historically consisted of radiation therapy to the entire breast for 5 weeks followed by a “boost” treatment of radiation specifically targeting the tumor area for an additional 5-8 days. This trial uses a shortened whole breast radiation treatment along with the “boost” at the same time instead of following the treatment to ensure a shorter treatment timeframe while still delivering the same amount of radiation that would be utilized in the standard way. This trial is being done to find out what happens with patients after receiving the shortened treatment timeframe of whole breast radiation simultaneously with the “boost” treatment allowing for reduced treatment time from 10-12 days down to only 5 days.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06295744.
Locations matching your search criteria
United States
Wisconsin
Johnson Creek
University of Wisconsin Carbone Cancer Center - Johnson CreekStatus: Active
Contact: Jessica Moore Schuster
Phone: 608-263-8500
Madison
University of Wisconsin Carbone Cancer Center - University HospitalStatus: Active
Contact: Jessica Moore Schuster
Phone: 608-263-8500
University of Wisconsin Carbone Cancer Center - Eastpark Medical CenterStatus: Active
Contact: Jessica Moore Schuster
PRIMARY OBJECTIVE:
I. To assess two-year cosmetic outcomes in patients treated with ultrashort whole breast irradiation (WBI) with simultaneous integrated boost (SIB).
SECONDARY OBJECTIVES:
I. To assess patient-reported outcome measures (PROMs) via BREAST-Q in patients treated with ultra-short WBI with SIB.
II. To assess acute toxicities in patients treated with ultra-short WBI with SIB.
III. To assess late toxicities in patients treated with ultra-short WBI with SIB.
IV. To assess ipsilateral breast tumor recurrence in patients treated with ultra-short whole breast irradiation with SIB.
V. To assess overall survival (OS) in patients treated with ultra-short WBI with SIB.
OUTLINE:
Patients undergo WBI and SIB in 5 fractions once daily (QD) for 5 days.
After completion of study treatment, patients are followed up at 6 weeks, 12, 24, 36, 48 and 60 months.
Trial PhaseNo phase specified
Trial Typetreatment
Lead OrganizationUniversity of Wisconsin Carbone Cancer Center - University Hospital
Principal InvestigatorJessica Moore Schuster