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Clinical Trial Summary

Hypofractionation with simultaneous integrated boost has been investigated in a few trials and appears to be safe and feasible with less lung toxicity in smaller studies. Investigators initiated this multicenter phase II prospective trial to analyse acute toxicity of hypofractionation with simultaneous integrated boost in patients with early breast cancer under the hypothesis that the ratio of patients with acute radiogenic toxicity Grad II according NCI-CTCAE amounts maximum 20%.


Clinical Trial Description

Hypofractionated radiotherapy of the breast 16 × 2.50 Gy with simultaneous integrated boost to the tumor bed (total dose within the boost volume 16 × 3.00 Gy). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01948726
Study type Interventional
Source University Hospital Schleswig-Holstein
Contact
Status Completed
Phase N/A
Start date December 2013
Completion date March 2015