Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Am Acad Dermatol. 2011 Jun;64(6):1074-84. doi: 10.1016/j.jaad.2010.04.027. Epub 2011 Mar 31.
Cyclosporin A (CsA) is frequently used in the treatment of severe atopic dermatitis (AD). Enteric-coated mycophenolate sodium (EC-MPS) may be an alternative with equal efficacy and fewer side effects.
The aim of this observer-blinded randomized controlled trial was to compare EC-MPS with CsA as long-term treatment in adult patients with severe AD.
Fifty five patients with AD were treated with CsA (5 mg/kg) in a 6-week run-in period. Thereafter, patients either received CsA (3 mg/kg; n = 26) or EC-MPS (1440 mg; n = 24) during a maintenance phase of 30 weeks and there was a 12-week follow-up period. Disease activity was measured using the objective SCORAD and serum thymus and activation-regulated chemokine (TARC) levels and side effects were registered.
During the first 10 weeks the objective SCORAD and serum TARC levels in the EC-MPS study arm were higher in comparison with the CsA study arm. In addition, 7 of the 24 patients treated with EC-MPS required short oral corticosteroid courses. During maintenance phase disease activity was comparable in both study arms. Side effects in both study arms were mild and transient. After study medication withdrawal, disease activity of the patients in the CsA study arm significantly increased compared with the EC-MPS study arm.
The nonblinding of patients and prescriber of rescue medication are limitations.
This study shows that EC-MPS is as effective as CsA as maintenance therapy in patients with AD. However, clinical improvement with EC-MPS is delayed in comparison with CsA. Clinical remission after stopping EC-MPS lasts longer compared with CsA.
环孢素 A(CsA)常用于治疗严重特应性皮炎(AD)。麦考酚钠肠溶片(EC-MPS)可能是一种疗效相当且副作用较少的替代药物。
本观察者盲法随机对照试验旨在比较 EC-MPS 与 CsA 作为长期治疗成人严重 AD 的药物。
55 例 AD 患者接受 CsA(5mg/kg)6 周导入期治疗。此后,患者在 30 周的维持期分别接受 CsA(3mg/kg,n=26)或 EC-MPS(1440mg,n=24)治疗,随后进行 12 周随访。采用客观 SCORAD 和血清胸腺和激活调节趋化因子(TARC)水平评估疾病活动度,并记录不良反应。
在最初的 10 周内,EC-MPS 组的客观 SCORAD 和血清 TARC 水平高于 CsA 组。此外,24 例接受 EC-MPS 治疗的患者中有 7 例需要短期口服皮质类固醇治疗。在维持期,两组的疾病活动度相当。两组的不良反应均轻微且短暂。停用研究药物后,CsA 组患者的疾病活动度明显高于 EC-MPS 组。
患者和抢救药物的处方者未设盲是本研究的局限性。
本研究表明,EC-MPS 作为 AD 患者的维持治疗与 CsA 同样有效。然而,与 CsA 相比,EC-MPS 的临床改善较为延迟。停止 EC-MPS 后,临床缓解持续时间长于 CsA。