Stern R S, Zierler S, Parrish J A
Cancer. 1982 Sep 1;50(5):869-72. doi: 10.1002/1097-0142(19820901)50:5<869::aid-cncr2820500511>3.0.co;2-v.
Using case-control methods, we separately evaluated the risk of noncutaneous and cutaneous malignancy associated with exposure to methotrexate as it is used in the treatment of severe psoriasis. An analysis of 26 cases of noncutaneous cancer and 104 matched controls revealed no association between the development of noncutaneous malignancy and exposure to methotrexate (relative risk = 0.96; upper bound 95% confidence interval = 2.0). An analysis of 80 cases of nonmelanoma skin cancer and 297 matched controls revealed a relative risk of 1.2 for the development of cutaneous malignancy among those with exposure to methotrexate (upper bound 95% confidence interval = 1.9). Our data suggest that methotrexate, as it is used in the treatment of severe psoriasis, does not increase the risk of noncutaneous or cutaneous malignancy.
采用病例对照研究方法,我们分别评估了在重度银屑病治疗中使用甲氨蝶呤与非皮肤恶性肿瘤及皮肤恶性肿瘤发生风险之间的关系。对26例非皮肤癌病例和104例匹配对照进行的分析显示,非皮肤恶性肿瘤的发生与甲氨蝶呤暴露之间无关联(相对风险=0.96;95%置信区间上限=2.0)。对80例非黑色素瘤皮肤癌病例和297例匹配对照进行的分析显示,暴露于甲氨蝶呤的人群发生皮肤恶性肿瘤的相对风险为1.2(95%置信区间上限=1.9)。我们的数据表明,用于重度银屑病治疗的甲氨蝶呤不会增加非皮肤或皮肤恶性肿瘤的风险。