This study is to determine whether acute treatment-associated adverse events following breast re-irradiation with aPBI are acceptably low and to assess local control following breast re-irradiation with aPBI. An exploratory aim is to assess cosmetic outcomes following breast re-irradiation with aPBI.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
aPBI, which is routinely used to treat patients who have previously not been irradiated, with a dose of 30 Gy in 5 fractions using a VMAT technique.
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, United States
Treatment-associated toxicity
Acceptably low acute treatment-associated adverse events following breast re-irradiation with aPBI.
Time frame: Within 1 year
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