Curtis Elizabeth Mary, Marks Jonathan Lewis
Department of Rheumatology, University Hospital Southampton, Southampton, Hampshire, UK.
Open Access Rheumatol. 2014 Mar 24;6:27-38. doi: 10.2147/OARRR.S41409. eCollection 2014.
Etanercept (ETN) is one of a number of biological therapies targeting the proinflammatory cytokine tumor necrosis factor-alpha that have demonstrated efficacy in the management of rheumatoid arthritis (RA). As experience has grown, a number of different treatment strategies have been investigated to ascertain the optimal conditions for use of ETN in RA and maximize the clinical gains from therapy. These have included the use of higher- and lower-dose treatment regimens, ETN as a monotherapy or in combination with other nonbiologic disease-modifying antirheumatic drugs, the use of ETN in very early clinical disease, and intraarticular ETN administration for resistant synovitis. Recent trials have focused on phased dose reduction or withdrawal of ETN in patients achieving low disease activity states or clinical remission. This review summarizes existing data regarding the optimal timing of ETN initiation and dosing regimens and also evaluates more recent evidence regarding dose-reduction strategies that offer the possibility of biologic-free remission in RA.
依那西普(ETN)是多种针对促炎细胞因子肿瘤坏死因子-α的生物疗法之一,已证明其在类风湿关节炎(RA)治疗中具有疗效。随着经验的积累,人们研究了多种不同的治疗策略,以确定依那西普在类风湿关节炎中使用的最佳条件,并使治疗的临床获益最大化。这些策略包括使用高剂量和低剂量治疗方案、依那西普单药治疗或与其他非生物改善病情抗风湿药联合使用、在疾病临床极早期使用依那西普以及关节内注射依那西普治疗耐药性滑膜炎。最近的试验集中在病情达到低活动状态或临床缓解的患者中逐步减少依那西普剂量或停药。本综述总结了关于依那西普起始治疗的最佳时机和给药方案的现有数据,并评估了关于减量策略的最新证据,这些策略为类风湿关节炎患者实现无生物制剂缓解提供了可能性。