Onal Sumru, Kazokoglu Haluk, Koc Aylin, Akman Mehmet, Bavbek Tayfun, Direskeneli Haner, Yavuz Sule
Uveitis Service, Department of Ophthalmology, Marmara University, School of Medicine, Istanbul, Turkey.
Arch Ophthalmol. 2011 Mar;129(3):288-94. doi: 10.1001/archophthalmol.2011.3.
To investigate the long-term efficacy and safety of low-dose and dose-escalating therapy of interferon alfa-2a in the treatment of Behçet uveitis.
This study included 37 patients with refractory Behçet panuveitis unresponsive to conventional immunosuppressive therapy. Induction interferon alfa-2a therapy was given as a daily dose of 3.0 million IU (MIU) subcutaneously for 14 days. Maintenance dose was achieved with 3.0 MIU 3 times per week given subcutaneously. The dosage was increased sequentially to 4.5, 6.0, and 9.0 MIU 3 times per week if uveitis relapses occurred. Total therapy duration was 24 months. Primary outcome measure was control of uveitis with quiescence during maintenance therapy. Ocular relapses per patient-year before and after initiation of interferon alfa-2a therapy and a corticosteroid-sparing effect were secondary outcomes. We also estimated the rate of remission after discontinuing interferon alfa-2a therapy.
During maintenance therapy, interferon alfa-2a controlled uveitis in 35 patients (95%). In 15 patients (41%), a maintenance dosage of 3.0 MIU 3 times per week controlled uveitis without any relapse. The rate of uveitis relapses decreased from 3.52 per patient-year before to 0.75 per patient-year after initiating interferon alfa-2a therapy. Seventeen patients were receiving systemic corticosteroids at the time of initiation of interferon therapy. During the maintenance stage, 9 patients were able to discontinue and 8 to taper systemic corticosteroid therapy. Survival analysis estimated that the rate of remission after discontinuation of interferon alfa-2a therapy was 76% by 3 months. The rate of remission remained stable thereafter.
A treatment protocol using a low-dose and dose-escalating therapy with interferon alfa-2a was able to control and achieve remission of uveitis in most patients with refractory ocular Behçet disease.
探讨低剂量及剂量递增疗法的干扰素α-2a治疗白塞氏葡萄膜炎的长期疗效及安全性。
本研究纳入37例对传统免疫抑制治疗无效的难治性白塞氏全葡萄膜炎患者。诱导期给予干扰素α-2a皮下注射,每日剂量300万国际单位(MIU),共14天。维持剂量为皮下注射3.0 MIU,每周3次。如果葡萄膜炎复发,剂量依次增加至每周3次的4.5、6.0和9.0 MIU。总治疗时长为24个月。主要观察指标是维持治疗期间葡萄膜炎的静止控制情况。干扰素α-2a治疗开始前后每位患者每年的眼部复发情况以及糖皮质激素节省效应为次要观察指标。我们还评估了停用干扰素α-2a治疗后的缓解率。
在维持治疗期间,干扰素α-2a使35例患者(95%)的葡萄膜炎得到控制。15例患者(41%)通过每周3次3.0 MIU的维持剂量控制了葡萄膜炎,未出现任何复发。干扰素α-2a治疗开始后,葡萄膜炎复发率从每位患者每年3.52次降至0.75次。17例患者在开始干扰素治疗时正在接受全身糖皮质激素治疗。在维持阶段,9例患者能够停用,8例患者能够逐渐减少全身糖皮质激素治疗。生存分析估计,停用干扰素α-2a治疗3个月后的缓解率为76%。此后缓解率保持稳定。
采用低剂量及剂量递增疗法的干扰素α-2a治疗方案能够控制并使大多数难治性眼部白塞氏病患者的葡萄膜炎得到缓解。