Pérez Pampín Eva, Gómez-Reino Carnota Juan Jesús
Servicio de Reumatología, Hospital Clínico Universitario, Complejo Hospitalario Universitario de Santiago de Compostela, Santiago de Compostela, La Coruña, España.
Med Clin (Barc). 2008 Feb 16;130(5):179-87. doi: 10.1157/13116323.
In the last decade, tumor necrosis factor (TNF) antagonists had supposed an important therapeutic advance in the treatment of patients with rheumatoid arthritis (RA) in both early and established RA. Three agents currently available--infliximab, etanercept, and adalimumab--have been designed to modify the biologic effects of TNF. Infliximab and adalimumab are monoclonal antibodies, whereas etanercept is a soluble protein, with different pharmacokinetic and pharmacodynamic properties, conditioning some possible adverse effects. Although comparative studies are not available, the 3 drugs have demonstrated efficacy and security, with a better quality of life of patients with RA. Infliximab, etanercept and adalimumab have been proved alone and in combination with methotrexate, with a better therapeutic, clinical, radiological and functional response in the group under combined therapy. Both clinical trials and post-market experience have demonstrated the security of these drugs, minimizing the risks with an adequate selection of patients.
在过去十年中,肿瘤坏死因子(TNF)拮抗剂被认为是类风湿关节炎(RA)早期和确诊患者治疗方面的一项重要治疗进展。目前可用的三种药物——英夫利昔单抗、依那西普和阿达木单抗——旨在改变TNF的生物学效应。英夫利昔单抗和阿达木单抗是单克隆抗体,而依那西普是一种可溶性蛋白,具有不同的药代动力学和药效学特性,这决定了一些可能的不良反应。虽然尚无比较研究,但这三种药物均已证明具有疗效和安全性,可改善RA患者的生活质量。英夫利昔单抗、依那西普和阿达木单抗已被证明单独使用以及与甲氨蝶呤联合使用时,联合治疗组在治疗、临床、放射学和功能反应方面表现更佳。临床试验和上市后经验均已证明这些药物的安全性,通过适当选择患者将风险降至最低。