Becker Jürgen C, Houben Roland, Vetter Claudia S, Bröcker Eva B
Department of Dermatology, Julius-Maximilians-University, Würzburg, Germany.
BMC Cancer. 2006 Jan 11;6:7. doi: 10.1186/1471-2407-6-7.
Since tacrolimus ointment was approved by the U.S. Food and Drug Administration (FDA) as a promising treatment for atopic dermatitis, it has been approved in more than 30 additional countries, including numerous European Union member nations. Moreover, in the current clinical routine the use of this drug is no longer restricted to the approved indication, but has been extended to a wide variety of inflammatory skin diseases including some with the potential of malignant transformation. So far, the side-effects reported from the topical use of tacrolimus have been relatively minor (e.g. burning, pruritus, erythema). Recently, however, the FDA reviewed the safety of topical tacrolimus, which resulted in a warning that the use of calcineurin inhibitors may be associated with an increased risk of cancer.
Oral lichen planus (OLP) was diagnosed in a 56-year-old women in February 1999. After several ineffective local and systemic therapeutic measures an off-label treatment of this recalcitrant condition using Tacrolimus 0.1% ointment was initiated in May 2002. After a few weeks of treatment most of the lesions ameliorated, with the exception of the plaques on the sides of the tongue. Nevertheless, the patient became free of symptoms which, however, reoccurred once tacrolimus was weaned, as a consequence treatment was maintained. In April 2005, the plaques on the left side of the tongue appeared increasingly compact and a biopsy specimen confirmed the suspected diagnosis of an oral squamous cell carcinoma.
The suspected causal relationship between topical use of tacrolimus and the development of a squamous cell carcinoma prompted us to test the notion that the carcinogenicity of tacrolimus may go beyond mere immune suppression. To this end, tacrolimus has been shown to have an impact on cancer signalling pathways such as the MAPK and the p53 pathway. In the given case, we were able to demonstrate that these pathways had also been altered subsequent to tacrolimus therapy.
自他克莫司软膏被美国食品药品监督管理局(FDA)批准作为特应性皮炎的一种有前景的治疗方法以来,它已在另外30多个国家获得批准,包括众多欧盟成员国。此外,在当前的临床常规中,这种药物的使用不再局限于批准的适应症,而是已扩展到多种炎症性皮肤病,包括一些有恶变可能的疾病。到目前为止,局部使用他克莫司报告的副作用相对较小(如烧灼感、瘙痒、红斑)。然而,最近FDA对局部使用他克莫司的安全性进行了审查,结果发出警告称,使用钙调神经磷酸酶抑制剂可能会增加患癌风险。
1999年2月,一名56岁女性被诊断为口腔扁平苔藓(OLP)。在采取了几种无效的局部和全身治疗措施后,2002年5月开始使用0.1%他克莫司软膏对这种顽固性疾病进行超适应症治疗。治疗几周后,除舌侧斑块外,大多数皮损有所改善。然而,患者症状消失,但在停用他克莫司后症状复发,因此维持治疗。2005年4月,舌左侧的斑块看起来越来越致密,活检标本证实了疑似口腔鳞状细胞癌的诊断。
局部使用他克莫司与鳞状细胞癌发生之间疑似的因果关系促使我们去验证他克莫司的致癌性可能不仅仅局限于单纯免疫抑制的观点。为此,已证明他克莫司会对癌症信号通路如丝裂原活化蛋白激酶(MAPK)和p53通路产生影响。在该病例中,我们能够证明在他克莫司治疗后这些通路也发生了改变。