Stern R S, Laird N, Melski J, Parrish J A, Fitzpatrick T B, Bleich H L
N Engl J Med. 1984 May 3;310(18):1156-61. doi: 10.1056/NEJM198405033101805.
A 5.7-year prospective study of 1380 patients treated for psoriasis with oral methoxsalen (8-methoxypsoralen) and ultraviolet A photochemotherapy (PUVA) revealed that after adjustment for exposures to ionizing radiation and topical tar preparations, the risk that cutaneous squamous-cell carcinoma would develop at least 22 months after the first exposure to PUVA was 12.8 times higher in patients exposed to a high dose than in those exposed to a low dose (95 per cent confidence interval, 5.8 to 28.5). No substantial dose-related increase was noted for basal-cell carcinoma. The dose-dependent risk of cutaneous squamous-cell carcinoma suggests that PUVA can act as an independent carcinogen. In our study, morbidity associated with these tumors has been limited, but further follow-up is needed. Meanwhile, patients treated with PUVA should be followed closely for the possible development of cutaneous squamous-cell carcinoma.
一项针对1380例接受口服甲氧沙林(8-甲氧基补骨脂素)和紫外线A光化学疗法(PUVA)治疗银屑病患者的5.7年前瞻性研究表明,在对电离辐射暴露和局部焦油制剂暴露进行校正后,首次暴露于PUVA至少22个月后发生皮肤鳞状细胞癌的风险,高剂量暴露患者比低剂量暴露患者高12.8倍(95%置信区间为5.8至28.5)。未观察到基底细胞癌有明显的剂量相关增加。皮肤鳞状细胞癌的剂量依赖性风险表明PUVA可作为一种独立致癌物。在我们的研究中,与这些肿瘤相关的发病率一直有限,但仍需要进一步随访。同时,接受PUVA治疗的患者应密切随访,以观察皮肤鳞状细胞癌的可能发生情况。