Hypofractionated Radiotherapy in Breast Cancer
Completed · Not applicable
Conditions studied: Cancer, Breast, Inflammation
In brief
As the number of breast cancer (BrCA) survivors has markedly increased, clinicians are now seeking to reduce treatment-related toxicities and inconveniences of treatment, namely the traditional 6 weeks of daily radiation treatment (XRT). Skin thickening, fibrosis, and edema are some of the most common acute and potentially long-term debilitating toxicities of BrCA XRT. The purpose of this study is to learn if three weeks of daily radiation treatment (RT) to the breast is safe in breast cancer patients who are usually prescribed 6 weeks of daily radiation after breast surgery (e.g. lumpectomy or mastectomy) as standard of care.
Key facts
- Study ID
- NCT03167359
- Run by
- Emory University
- People needed
- 74
- Starts
- 2010-12-01
- Expected to finish
- 2019-05-14
- Last updated by the study team
- 2021-05-07
Who can join
Age: any, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Participants must have one or more of the following characteristics and be eligible for breast or chest wall with or without regional nodal radiotherapy:
- Prior Chemotherapy for Breast Cancer
- Greater than 25 cm of breast separation (the largest distance on an axial slice of the planning CT simulation scan between the entry and exit points of the radiation beam on the body)
- Non-Caucasian Race
- Less than or equal to 50 years of age
- Requiring regional nodal irradiation without evidence of N3 disease
You may not qualify if…
- Males will be excluded
- Women who are pregnant or nursing a child may not take part in this study
Where it is running
- Emory University — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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