Radiation-Induced Skin Fibrosis Pathogenesis, Current Treatment Options, and Emerging Therapeutics

被引:101
|
作者
Borrelli, Mimi R. [1 ]
Shen, Abra H. [1 ]
Lee, Gordon K. [2 ]
Momeni, Arash [2 ]
Longaker, Michael T. [1 ,3 ]
Wan, Derrick C. [2 ]
机构
[1] Stanford Univ, Dept Surg, Sch Med, Hagey Lab Pediat Regenerat Med,Div Plast Surg, Stanford, CA USA
[2] Stanford Univ, Div Plast & Reconstruct Surg, Med Ctr, Palo Alto, CA USA
[3] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA USA
基金
美国国家卫生研究院;
关键词
fat grafting; fibrosis; radiation-induced fibrosis; radiodermatitis; CELL-ASSISTED LIPOTRANSFER; GROWTH-FACTOR-BETA; BREAST-CANCER; AUTOLOGOUS FAT; DOUBLE-BLIND; FOLLOW-UP; RANDOMIZED-TRIAL; SUPPORTIVE USE; RADIOTHERAPY; THERAPY;
D O I
10.1097/SAP.0000000000002098
中图分类号
R61 [外科手术学];
学科分类号
摘要
Radiotherapy (RT) has become an indispensable part of oncologic treatment protocols for a range of malignancies. However, a serious adverse effect of RT is radiodermatitis; almost 95% of patients develop moderate to severe skin reactions following radiation treatment. In the acute setting, these can be erythema, desquamation, ulceration, and pain. Chronically, soft tissue atrophy, alopecia, and stiffness can be noted. Radiodermatitis can delay oncologic treatment protocols and significantly impair quality of life. There is currently a paucity of effective treatment options and prevention strategies for radiodermatitis. Importantly, recent preclinical and clinical studies have suggested that fat grafting may be of therapeutic benefit, reversing detrimental changes to soft tissue following RT. This review outlines the damaging effects of RT on the skin and soft tissue as well as discusses available treatment options for radiodermatitis. Emerging strategies to mitigate detrimental, chronic radiation-induced changes are also presented.
引用
收藏
页码:S59 / S64
页数:6
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