Objective, Clinician- and Patient-Reported Evaluation of Late Toxicity Following Adjuvant Radiation for Early Breast Cancer: Long-Term Follow-Up Results of a Randomised Series

Author:

Dejonckheere Cas Stefaan1ORCID,Abramian Alina2,Lindner Kira2,Bachmann Anne2,Layer Katharina1,Anzböck Teresa3,Layer Julian Philipp14ORCID,Sarria Gustavo Renato1ORCID,Scafa Davide1ORCID,Koch David1,Leitzen Christina1ORCID,Kaiser Christina2,Faridi Andree2,Schmeel Leonard Christopher1ORCID

Affiliation:

1. Department of Radiation Oncology, University Hospital Bonn, 53127 Bonn, Germany

2. Department of Gynaecology, Division of Senology, University Hospital Bonn, 53127 Bonn, Germany

3. Department of Gynaecology, Division of Gynaecology and Gynaecological Oncology, University Hospital Bonn, 53127 Bonn, Germany

4. Institute of Experimental Oncology, University Hospital Bonn, 53127 Bonn, Germany

Abstract

Background and Purpose: This study aimed to differentially assess the frequency and severity of late radiation-induced toxicity following adjuvant whole-breast irradiation for early breast cancer with conventional fractionation (CF) and moderate hypofractionation (mHF). Materials and Methods: Patients recruited in a previous randomised controlled trial comparing acute toxicity between CF and mHF without disease recurrence were included in a post hoc analysis. Spectrophotometric and ultrasonographic examinations were performed for an objective evaluation and subsequent comparison of long-term skin toxicity. Furthermore, patient- and clinician-reported outcomes were recorded. Results: Sixty-four patients with a median age of 58 (37–81) years were included. The median follow-up was 57 (37–73) months. A total of 55% underwent CF and 45% mHF. A total of 52% received a sequential boost to the tumour bed. A significant decrease in mean L* (p = 0.011) and an increase in a* (p = 0.040) and b* values (p < 0.001) were observed, indicating hyperpigmentation. In comparison with the non-irradiated breast, there was a significant increase in both cutis (+14%; p < 0.001) and subcutis (+17%; p = 0.011) thickness, significantly more pronounced in CF patients (p = 0.049). In CF patients only, a sequential boost significantly increased the local cutis thickness and oedema compared to non-boost regions in the same breast (p = 0.001 and p < 0.001, respectively). Conclusions: mHF objectively resulted in reduced long-term skin toxicity compared to CF. A sequential boost increased the local fibrosis rate in CF, but not in mHF. This might explain the subjectively reported better cosmetic outcomes in patients receiving mHF and reinforces the rationale for favouring mHF as the standard of care.

Publisher

MDPI AG

Subject

General Medicine

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