摘要
目的:观察重组人Ⅱ型肿瘤坏死因子受体抗体融合蛋白(rhTNFR:Fc商品名:益赛普)联合抗风湿药物(甲氨蝶呤、来氟米特)治疗中重度银屑病的疗效及安全性。方法:选取本院就诊的78例中重度银屑病患者,其中45例应用rhTNFR:Fc联合甲氨蝶呤、来氟米特治疗为观察组,33例采用单纯抗风湿药物(甲氨喋呤联合来氟米特)治疗为对照组。观察并比较用药前及用药后2周、4周、8周、12周、24周两组的PASI指数及不良反应。结果:治疗8周后两组的PASI50差异有统计学意义(P<0.05),治疗12周及24周后两组PASI50、PASI75、PASI90的比例高于对照组,差异均有统计学意义(P<0.05),两组之间不良反应发生率比较差异无统计学意义(P>0.05)。结论:rhTNFR:Fc联合甲氨蝶呤、来氟米特治疗中重度银屑病疗效显著,值得临床推广。
Objective: To observe the clinical effiency and safety of Recombinant Human Tumor Necrosis Factor-α ReceptorⅡ:Ig G Fc Fusion Protein(rhTNFR),combined with anti rheumatic drugs(methotrexate,leflunomide) in treatment of moderate to severe plaque psoriasis.Methods: 78 patients of moderate to severe plaque psoriasis treated in our department were selected,45 cases of the observation group treated with rhTNFR: Fc combined with methotrexate(MTX) and leflunomide(LEF),33 cases of the control group treated with MTX + LEF.The severity index scores(PASI) and adverse reaction before treatment and at 2,4,8,12 and 24 weeks after treatment were observed.Results: After 8 weeks of treatment,the difference of PASI50 between the two groups was statistically significant(P < 0.05).After 12 weeks and 24 weeks,the ratio of PASI50,PASI75 and PASI90 in the two groups was significantly higher than that in the control group,and the differences were statistically significant(P < 0.05).There was no significant difference in the incidence of adverse reactions between the two groups(P > 0.05).Conclusion: It's effective and safety of rhTNFR: Fc combined with MTX and LEF for the treatment of moderate to severe plaque psoriasis,which is worthy of clinical promotion.
出处
《川北医学院学报》
CAS
2017年第6期852-854,共3页
Journal of North Sichuan Medical College
基金
四川省卫计委科研项目(110599)
宜宾市科技局基金项目(2012SF004)