Cush John J
Presbyterian Hospital of Dallas, 8200 Walnut Hill Lane, Dallas, TX 75231, USA.
Rheum Dis Clin North Am. 2004 May;30(2):237-55, v. doi: 10.1016/j.rdc.2004.02.003.
Beginning in 1998, a surge of new agents has expanded treatment options for rheumatoid arthritis (RA) patients. Although the disease modifying potential of these agents is encouraging, their use must be weighed against an evolving array of new safety concerns. Because of the popularity of these agents with patients and rheumatologists alike, clinicians must be prepared to discuss the potential risks associated with novel disease-modifying antirheumatic drugs and biologic therapies as they begin to appear with greater frequency in practice. This article discusses the safety issues arising from clinical trial and postmarketing experience with several new and commonly used agents, with specific emphasis on adalimumab, etanercept, infliximab, anakinra, and leflunomide.
从1998年开始,大量新药物的出现扩大了类风湿关节炎(RA)患者的治疗选择。尽管这些药物的疾病修饰潜力令人鼓舞,但在使用时必须权衡一系列新出现的安全问题。由于这些药物在患者和风湿病学家中都很受欢迎,随着新型疾病修饰抗风湿药物和生物疗法在临床实践中出现的频率越来越高,临床医生必须准备好讨论与之相关的潜在风险。本文讨论了几种新的常用药物在临床试验和上市后经验中出现安全问题,特别强调了阿达木单抗、依那西普、英夫利昔单抗、阿那白滞素和来氟米特。