Lindelöf B, Sigurgeirsson B, Tegner E, Larkö O, Johannesson A, Berne B, Ljunggren B, Andersson T, Molin L, Nylander-Lundqvist E, Emtestam L
Division of Dermatology, Karolinska Institute, Danderyd Hospital, S-182 88 Stockholm, Sweden.
Br J Dermatol. 1999 Jul;141(1):108-12. doi: 10.1046/j.1365-2133.1999.02928.x.
There is concern about the long-term carcinogenic effects of psoralen and ultraviolet A radiation (PUVA) for treatment of skin disorders. Many authors have found an increased risk for cutaneous squamous cell carcinoma (SCC). Except in anecdotal reports, malignant melanoma had not been observed in patients treated with PUVA until recently. In the U.S.A., a 16-centre prospective study of 1380 patients showed for the first time that there might also be an increased risk for malignant melanoma in patients treated with high cumulative dosages of PUVA. We have therefore followed up the Swedish PUVA cohort until 1994. This cohort had previously been followed up until 1985. Information from 4799 Swedish patients (2343 men, 2456 women) who had received PUVA between 1974 and 1985 was linked to the compulsory Swedish Cancer Registry in order to identify individuals with cancer. The average follow-up period was 15.9 years for men and 16.2 for women. We did not find any increased risk for malignant melanoma in our total cohort of 4799 patients treated with PUVA or in a subcohort comprising 1867 patients followed for 15-21 years. For cutaneous SCC there was an increase in the risk: the relative risk was 5.6 (95% confidence interval, CI 4. 4-7.1) for men and 3.6 (95% CI 2.1-5.8) for women. Significant (P < 0.05) increases were also found in the incidence of respiratory cancer in men and women and of kidney cancer in women. In conclusion, we did not find any increased risk for malignant melanoma in our patients treated with high doses of PUVA and followed up for a long time. We confirm previous reports of an increase in the incidence of cutaneous SCC in patients treated with PUVA, and recommend that patients should be carefully selected for PUVA and rigorously followed up.
人们担心补骨脂素与紫外线A辐射(PUVA)治疗皮肤疾病的长期致癌作用。许多作者发现皮肤鳞状细胞癌(SCC)风险增加。除了轶事报道外,直到最近在用PUVA治疗的患者中尚未观察到恶性黑色素瘤。在美国,一项针对1380名患者的16中心前瞻性研究首次表明,接受高累积剂量PUVA治疗的患者患恶性黑色素瘤的风险也可能增加。因此,我们对瑞典PUVA队列进行了随访,直至1994年。该队列此前已随访至1985年。将1974年至1985年间接受PUVA治疗的4799名瑞典患者(2343名男性,2456名女性)的信息与瑞典强制性癌症登记处相关联,以识别患有癌症的个体。男性的平均随访期为15.9年,女性为16.2年。在接受PUVA治疗的4799名患者的整个队列中,或在由1867名随访15 - 21年的患者组成的亚队列中,我们未发现恶性黑色素瘤风险增加。对于皮肤SCC,风险有所增加:男性的相对风险为5.6(95%置信区间,CI 4.4 - 7.1),女性为3.6(95%CI 2.1 - 5.8)。男性和女性的呼吸道癌发病率以及女性的肾癌发病率也有显著(P < 0.05)增加。总之,在接受高剂量PUVA治疗并长期随访的患者中,我们未发现恶性黑色素瘤风险增加。我们证实了先前关于接受PUVA治疗的患者皮肤SCC发病率增加的报道,并建议应仔细选择接受PUVA治疗的患者并进行严格随访。