Topical Deferoxamine Alleviates Skin Injury and Normalizes Atomic Force Microscopy Patterns Following Radiation in a Murine Breast Reconstruction Model. Issue 5 (November 2018)

• Record Type: Journal Article
• Authors: Snider, Alicia E.; Lynn, Jeremy V.; Urlaub, Kevin M.; Donneys, Alexis; Polyatskaya, Yekaterina; Nelson, Noah S.; Ettinger, Russell E.; Gurtner, Geoffrey C.; Banaszak Holl, Mark M.; Buchman, Steven R.
• Is Part Of: Annals of plastic surgery. Volume 81:Issue 5(2018)
• Publication Date: 2018-11
• Subjects: breast expander -- cancer -- fibrosis -- skin ulceration -- type I collagen; Surgery, Plastic -- Periodicals; 617.95205
• DOI: 10.1097/SAP.0000000000001592
• Languages: English
• ISSNs: 0148-7043

Abstract

Abstract : Background: Breast cancer is most commonly managed with a combination of tumor ablation, radiation, and/or chemotherapy. Despite the oncologic benefit of these treatments, the detrimental effect of radiation on surrounding tissue challenges the attainment of ideal breast reconstruction outcomes. The purpose of this study was to determine the ability of topical deferoxamine (DFO) to reduce cutaneous ulceration and collagen disorganization following radiotherapy in a murine model of expander-based breast reconstruction. Methods: Female Sprague-Dawley rats (n = 15) were divided into 3 groups: control (expander), XRT (expander + radiation), and DFO (expander + radiation + deferoxamine [DFO]). Expanders were placed in a submusculocutaneous plane in the right upper back and ultimately filled to 15 mL. Radiation was administered via a fractionated dose of 28 Gy. Deferoxamine was delivered topically for 10 days following radiation. After a 20-day recovery period, skin ulceration and dermal type I collagen organization were analyzed. Results: Compared with control, the XRT group demonstrated a significant increase in skin ulceration (3.7% vs 43.3%, P = 0.00) and collagen fibril disorganization (26.3% vs 81.8%, P = 0.00). Compared with the XRT group, treatment with topical DFO resulted in a significant reduction in ulceration (43.3% vs 7.0%, P = 0.00) and fibril disorganization (81.8% vs 15.3%, P = 0.00). There were no statistical differences between the control and DFO groups in skin ulceration or collagen disorganization. Conclusions: This study suggests topical DFO is capable of reducing skin ulceration and type I collagen fibril disorganization following radiotherapy. This novel application of DFO has potential to enhance expander-based breast reconstruction outcomes and improve quality of life for women suffering the devastating effects of breast cancer.