Skin toxicity (including erythema, desquamation, necrosis/ ulceration, breast edema and bleeding) for grades 0/1/2/3 was distributed as 24.3/61.8/13.6/0.3% at the completion of treatment. The most common acute toxicities at completion of treatment were erythema and breast edema. The only patient with a documented grade 3 bleeding presented this already before start of radiotherapy. 6-months follow-up data was available for 225 patients: with fibrosis grade 0/1/2 in 75.6/20.0/4.4%, skin telangiectasia grade 0/1/2 in 95.6/4.0/0.4%, pigmentation changes grade 0/1/2 in 71.0/27.7/1.3% cases. Patient-reported cosmetic results 6 months post treatment were evaluated in 55.0/41.7/2.3/0.9% cases as excellent/good/fair/poor. Results of 1-year follow-up (available from 137 patients) were comparable: fibrosis grade 0/1/2 in 78.1/20.4/1.5%, no skin telangiectasia (only grade 0), pigmentation changes grade 0/1/2 in 78.7/20.6/0.7% cases. 1-year patient-reported cosmetic results were evaluated in 62.2/34.1/3.7% as excellent/good/fair. 31 patients examined on the 2-year follow-up visit presented with fibrosis grade 0/1 in 93.5/6.5%, pigmentation changes grade 0/1/2 in 80.6/16.1/3.2%. PROM of cosmetic results were evaluated in 59.4/34.4/3.1/3.1% as excellent/good/fair/poor.
Ipsilateral breast tumor recurrence developed in 2/391 patients (0.5%) (one in-boost, one marginal to the 40 Gy volume, both triple negative), distant metastatic disease developed in 6 patients (1.5%) at the time of this analysis. No cancer related mortality was observed so far.