Prevention and Management of Radiation Dermatitis: Variation Based on Anatomic Target

Main Article Content

Alexandra DeVries https://orcid.org/0009-0008-6576-2432
Wilhelmina Lam, DO, MPH https://orcid.org/0000-0001-6709-4281
Alec Lawson https://orcid.org/0009-0001-5147-9803
Aysham Chaudry, DO https://orcid.org/0009-0005-5303-5850
Robert Vanaria
Mark S. Nestor, MD, PhD

Keywords

Radiation Dermatitis, Superfical Radiation Therapy, SRT, non melanoma skin cancer, NMSC

Abstract

Radiation dermatitis (RD) is a universal adverse consequence of radiation therapy (RT) and is associated with a dramatic barrier dysfunction and inflammation. The management of RD depends upon the anatomic target: internal malignancy (IM) versus skin cancer (NMSC). For IM, it is critical to address RD for both morbidity and the ability to continue treatment. While multiple treatment options exist, barrier repair using a ceramide dominant triple lipid prescription formulation has been shown to have significant benefit. For NMSC, radiation dermatitis is a necessary side effect potentially increasing the effect of radiation therapy. Barrier repair should occur after treatment is completed.

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