Breast cancer. Malignant neoplasms of breast
Conditions
Interventions
Intervention 1: Intervention group: Concomitant boost with 10 Gray in 5 fraction, one session every weekend. Intervention 2: Control group: Sequential radiation boost, 10 Gray in 5 fraction at the end
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Women with pathologically proven breast cancer Age 18-75 Undergoing breast conserving surgery Early staged breast cancer (T1-3,N0-1)
Exclusion criteria
Exclusion criteria: Previous skin disease Previous breast radiation Previous cancer Positive margin on surgery Multifocal disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute skin toxicity of breast radiotherapy. Timepoint: Weekly during radiotherapy. Method of measurement: Physical exam and grading the skin side effects via Common Terminology Criteria for Adverse Events version 4.;Cosmetic outcome. Timepoint: 6 and 12 months after radiotherapy. Method of measurement: Physical exam and scoring according to Harvard criteria. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReyhane Bayani
Tehran University of Medical Sciences
Outcome results
None listed