Risk of Non-melanoma Skin Cancer in Patients with Atopic Dermatitis Treated with Oral Immunosuppressive Drugs

被引:12
|
作者
Garritsen, Floor M. [1 ]
Van der Schaft, Jorien [1 ]
Van den Reek, Juul M. [2 ]
Politiek, Klaziena [3 ]
Van Osmedendorp, Harmieke [1 ]
Van Dijk, Marijke [4 ]
Hijnen, Dirk J. [1 ]
De Graaf, Marlies [1 ]
Bruijnzeel-Koomen, Carla A. [1 ]
De Jong, Elke M. [2 ,5 ]
Schuttelaar, Marie-Louise A. [3 ]
De Bruin-Weller, Marjolein S. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Dermatol, Utrecht, Netherlands
[2] Univ Med Ctr Nijmegen, Dept Dermatol, Nijmegen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Dermatol, Groningen, Netherlands
[4] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[5] Radboud Univ Nijmegen, Dept Dermatol, Nijmegen, Netherlands
关键词
atopic dermatitis; oral immunosuppressive drugs; non-melanoma skin cancer; INFLAMMATORY-BOWEL-DISEASE; COATED MYCOPHENOLATE SODIUM; SQUAMOUS-CELL CARCINOMA; DAILY PRACTICE COHORT; LONG-TERM TREATMENT; CYCLOSPORINE-A; ADULT PATIENTS; TRANSPLANT RECIPIENTS; ORGAN-TRANSPLANTATION; SINGLE-CENTER;
D O I
10.2340/00015555-2637
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
There is uncertainty about the risk of developing non-melanoma skin cancer (NMSC), including basal cell carcinoma and squamous cell carcinoma (SCC), in patients with atopic dermatitis (AD) treated with oral immunosuppressive drugs. A total of 557 patients with AD treated with these drugs in the University Medical Center Utrecht and Groningen, the Netherlands, were analysed. NMSC after oral immunosuppressive treatment was reported in 18 patients (3.2%). The standardized incidence ratio for developing SCC was 13.1 (95% confidence interval (CI) 6.5-19.7). Patients developing NMSC were older at the start of therapy (p < 0.001) and data lock (p < 0.001) compared with patients without NMSC. No significant differences were found in sex, cumulative days of oral immunosuppressive drugs and follow-up between these groups (p = 0.42, p = 0.88, and p = 0.34, respectively). In interpreting these results it is important to include other factors, such as lack of association between treatment duration and tumour development and the long interval between treatment discontinuation and tumour development in some patients.
引用
收藏
页码:724 / 730
页数:7
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