Fitzpatrick skin phototype is an independent predictor of squamous cell carcinoma risk after solid organ transplantation

被引:72
作者
Gogia, Ravinder [1 ]
Binstock, Maxwell [1 ]
Hirose, Ryutaro [2 ]
Boscardin, W. John [3 ]
Chren, Mary-Margaret [1 ]
Arron, Sarah T. [1 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94115 USA
[2] Univ Calif San Francisco, Dept Surg, Div Transplantat, San Francisco, CA 94115 USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94115 USA
基金
美国国家卫生研究院;
关键词
Fitzpatrick skin type; immunosuppression; organ transplant recipient; phototype; solid organ transplantation; squamous cell carcinoma; PROPORTIONAL HAZARDS MODELS; IMMUNOSUPPRESSIVE THERAPY; CANCER; RECIPIENTS; VALIDITY; EPIDEMIOLOGY; MANAGEMENT; KIDNEY;
D O I
10.1016/j.jaad.2012.09.030
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Solid organ transplant recipients (OTR) are at an increased risk of developing squamous cell carcinoma (SCC) of the skin after transplantation. In predominantly white cohorts, Fitzpatrick skin type (FST) has been reported to be a risk factor for developing posttransplantation skin cancers. Objective: Our goal was to determine if FST is a statistically significant risk factor for the development of SCC after solid organ transplantation in a diverse US population of OTR. Methods: A cohort of OTR completed a questionnaire of demographic factors, transplant type, FST, and skin cancer history. Univariate and multivariate analyses were performed to determine the risk factors for development of SCC after transplantation. Results: As expected, male subjects had an increased risk for SCC compared with female subjects (P = .02), and those aged 50 years and older at the time of transplantation were more likely to develop SCC compared with those younger than 50 years (P < . 001). The risk of SCC increased with each incremental decrease in FST, from FST VI to FST I (linear test for trend P < . 001). Limitations: Our questionnaire did not ask specifically about immunosuppressive medications; instead, organ transplant category was used as a proxy for level of immunosuppression. Conclusions: FST, a patient-reported variable, is an independent risk factor for the development of SCC in OTR, and should be elicited from patients who have gone or will undergo organ transplantation. (J Am Acad Dermatol 2013;68:585-91.)
引用
收藏
页码:585 / 591
页数:7
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