Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.
BioDrugs. 2000 Nov;14(5):319-29. doi: 10.2165/00063030-200014050-00004.
The aim of this review is to summarise the available literature regarding the epidemiology and proposed mechanisms of skin cancer development in organ transplant recipients who are receiving lifelong treatment with immunosuppressive therapy and to review the different strategies for managing complications in this group of patients. Organ transplantation is complicated by an increased incidence of certain cancers, of which non-Hodgkin's lymphoma, Kaposi's sarcoma and squamous cell carcinoma are the most common. The most important risk factor for these cancers is immunosuppressive therapy. The relative importance of different immunosuppressive therapy regimens in relation to the development of skin cancer is still unclear. Immunosuppression per se may play the most important role, but other mechanisms, which are independent of host immunity and which may be different for the various agents used, may also be of importance for the increased risk of cancer. Apart from immunosuppressive therapy, exposure to sunlight and infection with human papillomaviruses are believed to be the most important risk factors for the development of cutaneous squamous cell carcinoma in organ transplant recipients. Human papillomaviruses, no doubt, benefit considerably from immunosuppression, as is indicated by the large number of warts found in these patients, but many questions remain unanswered about their significance in cutaneous oncogenesis. The E6 protein from a range of cutaneous human papillomavirus types effectively inhibits apoptosis in response to ultraviolet light damage. It is, therefore, conceivable that the development of skin cancer in organ transplant recipients is the result of a complex interplay between exposure to ultraviolet radiation, human papillomavirus infection and genetic predisposition. Measures for protection from the sun are important for reducing the risk of skin cancer in organ transplant recipients. Regular surveillance of patients with skin problems and easy access to a dermatologist for these patients is advised. Changing the immunosuppressive regimen from azathioprine to cyclosporin or vice versa does not seem to relieve the skin problems. Tapering the immunosuppressive therapy to the lowest possible dose may be of some advantage. Oral retinoids, e.g. acitretin, have some effect in reducing the number of keratotic skin lesions and in the prevention of skin cancer in organ transplant recipients. Resurfacing the back of the hand can be a successful treatment for patients with multiple skin cancers on the back of the hand and can be used prophylactically in patients with severely actinically damaged skin.
本文旨在总结器官移植受者在接受终生免疫抑制治疗的情况下皮肤癌发生的流行病学和发病机制,并综述该人群并发症的处理策略。器官移植后发病率增加的癌症中,非霍奇金淋巴瘤、卡波西肉瘤和鳞状细胞癌最为常见。这些癌症最重要的危险因素是免疫抑制治疗。不同免疫抑制治疗方案与皮肤癌发展的关系尚不清楚,免疫抑制本身可能起最重要作用,但其他独立于宿主免疫的机制,对于各种药物应用的不同可能也会增加癌症风险。除免疫抑制治疗外,阳光照射和人乳头瘤病毒感染被认为是器官移植受者皮肤鳞状细胞癌发生的最重要危险因素。人乳头瘤病毒无疑受益于免疫抑制,因为这些患者有大量的疣,但它们在皮肤发生肿瘤中的意义仍有许多问题尚未解决。来自多种皮肤型人乳头瘤病毒的 E6 蛋白有效地抑制了紫外线损伤的细胞凋亡,因此,器官移植受者皮肤癌的发生可能是暴露于紫外线辐射、人乳头瘤病毒感染和遗传易感性之间复杂相互作用的结果。采取防晒措施对降低器官移植受者皮肤癌的风险很重要。建议定期监测有皮肤问题的患者,并为这些患者提供方便的皮肤科医生。将免疫抑制方案从硫唑嘌呤改为环孢素或反之,似乎并不能缓解皮肤问题。将免疫抑制治疗降至最低可能会有一定的好处。口服维甲酸,如阿维 A 酯,对减少角化皮肤病变的数量和预防器官移植受者皮肤癌有一定效果。在手背部进行表面重塑治疗在手背部有多发性皮肤癌的患者中是一种有效的治疗方法,并且可以在皮肤严重光损伤的患者中预防性使用。