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Worst Reported Treatment-Related Adverse Event–Grade 3 in 4/52 Patients (7.7%)
| G3 Adverse Event* | n (%) | Months Since Start of Treatment (Mean) |
|---|---|---|
| Radiation Dermatitis | 1 (2%) | 1.2 |
| Myositis | 1 (2%) | 5.3 |
| Skin Fibrosis | 2 (4%) | 45.4 |
| Telangiectasia | 2 (4%) | 61.2 |
| Fibrosis - Cosmesis | 1 (2%) | 85.3 |
3 of 4 patients reported >1 adverse event
