This phase II trial studies how well hypofractionated radiation therapy works in treating patients with stage II-III breast cancer undergoing total nodal irradiation. 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.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT02958774.
PRIMARY OBJECTIVE:
I. To determine lymphedema rates in patients requiring RNI who receive hypofractionated radiation.
SECONDARY OBJECTIVES:
I. To determine local control benefit in patients receiving hypofractionated radiation for breast cancer requiring regional nodal irradiation.
II. To determine whether cosmetic outcomes at short term and long term follow-up for patients receiving radiation to the regional nodal regions.
III. To determine changes in quality of life, using the FACT-B+4 breast quality of life questionnaire, for patients undergoing hypofractionated radiation.
OUTLINE:
Beginning 3-12 weeks after surgery or chemotherapy, patients undergo hypofractionated radiation therapy daily (QD) for 4-4.5 weeks.
After completion of study treatment, patients are followed up between 14 and 90 days, at 6 and 18 months, and then annually until 5 years after end of treatment.
Lead OrganizationUniversity of Kansas Cancer Center
Principal InvestigatorShane Richard Stecklein