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口服补骨脂素及紫外线A光(PUVA)治疗银屑病与非黑素瘤皮肤癌的持续风险。PUVA随访研究。

Oral psoralen and ultraviolet-A light (PUVA) treatment of psoriasis and persistent risk of nonmelanoma skin cancer. PUVA Follow-up Study.

作者信息

Stern R S, Liebman E J, Väkevä L

机构信息

Department of Dermatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

J Natl Cancer Inst. 1998 Sep 2;90(17):1278-84. doi: 10.1093/jnci/90.17.1278.

Abstract

BACKGROUND/METHODS: The treatment of psoriasis with high-dose exposure to oral psoralen and ultraviolet-A light (i.e., PUVA) substantially increases the risk of cutaneous squamous cell cancer, but not of basal cell cancer, within a decade of beginning treatment. To assess the persistence of cancer risk among individuals treated with PUVA, including those who discontinued therapy long ago and those without substantial exposure to other carcinogens, we prospectively studied a cohort of 1380 patients with psoriasis who were first treated during the period from January 1, 1975, through October 1, 1976, and evaluated risk factors associated with the development of cutaneous squamous cell cancers and basal cell cancers after 1985.

RESULTS

From 1975 through 1996, 237 patients developed 1422 cutaneous squamous cell cancers. From 1986 through 1996, 135 (12.5%) of 1081 patients without a prior squamous cell cancer developed 593 such tumors. From 1975 through 1997, 247 patients developed 1042 basal cell cancers; these patients included 151 individuals with a first basal cell cancer after 1985. Among those without a squamous cell or a basal cell cancer in the first decade of the prospective study, a strong dose-related increase in the risk of squamous cell cancer was observed in the subsequent decade (adjusted relative risk [> or =337 treatments versus <100 treatments] = 8.6; 95% confidence interval = 4.9-15.2). Risk of basal cell cancer was substantially increased only in those patients exposed to very high levels of PUVA (> or =337 treatments).

CONCLUSIONS

High-dose exposure to PUVA is associated with a persistent, dose-related increase in the risk of squamous cell cancer, even among patients lacking substantial exposure to other carcinogens and among patients without substantial recent exposure to PUVA. Exposure to PUVA has far less effect on the risk of basal cell cancer. The use of PUVA for psoriasis should be weighed against the increased cancer risk.

摘要

背景/方法:高剂量口服补骨脂素并联合紫外线A光(即PUVA)治疗银屑病,在开始治疗后的十年内会大幅增加皮肤鳞状细胞癌的风险,但不会增加基底细胞癌的风险。为了评估接受PUVA治疗的个体患癌风险的持续性,包括那些很久以前就停止治疗的人和那些没有大量接触其他致癌物的人,我们对1380例银屑病患者进行了前瞻性研究,这些患者于1975年1月1日至1976年10月1日期间首次接受治疗,并评估了1985年后与皮肤鳞状细胞癌和基底细胞癌发生相关的危险因素。

结果

从1975年到1996年,237例患者发生了1422例皮肤鳞状细胞癌。从1986年到1996年,1081例既往无鳞状细胞癌的患者中有135例(12.5%)发生了593例此类肿瘤。从1975年到1997年,247例患者发生了1042例基底细胞癌;这些患者包括151例在1985年后首次发生基底细胞癌的个体。在前瞻性研究的第一个十年中无鳞状细胞癌或基底细胞癌的患者中,在随后的十年中观察到鳞状细胞癌风险与剂量相关的显著增加(调整后的相对风险[≥337次治疗与<100次治疗相比]=8.6;95%置信区间=4.9-15.2)。仅在那些接受非常高剂量PUVA治疗(≥337次治疗)的患者中,基底细胞癌的风险大幅增加。

结论

高剂量暴露于PUVA与鳞状细胞癌风险的持续、剂量相关增加有关,即使在缺乏大量接触其他致癌物的患者以及近期未大量接触PUVA的患者中也是如此。PUVA暴露对基底细胞癌风险的影响要小得多。使用PUVA治疗银屑病应权衡其增加的癌症风险。

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