Tugal-Tutkun Ilknur, Mudun Abdulbaki, Urgancioglu Meri, Kamali Sevil, Kasapoglu Esen, Inanc Murat, Gül Ahmet
Istanbul University, Turkey.
Arthritis Rheum. 2005 Aug;52(8):2478-84. doi: 10.1002/art.21231.
To investigate the effect of infliximab on the frequency of uveitis attacks and the visual prognosis in male patients with Behçet's disease in whom uveitis was resistant to combination therapy with corticosteroids, azathioprine, and cyclosporine.
The study group comprised patients who were receiving combination therapy but experienced at least 2 attacks of posterior uveitis/panuveitis or retinal vasculitis during the 6-month period prior to enrollment. Infliximab infusions (5 mg/kg) were administered at weeks 0, 2, 6, and 14. Weeks 0-22 were defined as the infusion period, and weeks 23-54 were defined as the observation period. Patients continued to receive azathioprine and corticosteroids, but cyclosporine was discontinued after the screening visit. The primary outcome measures were the absence of uveitis attacks during the infusion period (remission), and the absence of uveitis attacks throughout the study period (sustained remission).
Thirteen patients were enrolled in the study. Thirty-two uveitis attacks involving the posterior segment occurred during the previous-treatment period. During the infusion period, 4 patients (30.8%) remained attack-free, and 9 patients had a total of 13 uveitis attacks. Ten of these attacks (76.9%) occurred at either week 14 or week 22. One of 13 patients fulfilled the definition of sustained remission, and the remaining 12 patients had a total of 36 uveitis attacks during the observation period. The mean number of uveitis attacks and daily corticosteroid doses were significantly lower during the infusion period than during the previous-treatment period or the observation period. Although potential visual acuity was regained following infliximab infusion, this beneficial effect was not preserved until week 54. None of the patients experienced a serious adverse event.
The results of this trial suggest that infliximab is effective in suppressing the occurrence of uveitis attacks, has a corticosteroid-sparing effect, and has favorable implications for the visual prognosis of patients with resistant Behçet's uveitis.
探讨英夫利昔单抗对葡萄膜炎发作频率的影响以及对糖皮质激素、硫唑嘌呤和环孢素联合治疗无效的白塞病男性患者的视力预后情况。
研究组包括在入组前6个月内接受联合治疗但至少发生2次后葡萄膜炎/全葡萄膜炎或视网膜血管炎发作的患者。在第0、2、6和14周给予英夫利昔单抗输注(5mg/kg)。第0 - 22周定义为输注期,第23 - 54周定义为观察期。患者继续接受硫唑嘌呤和糖皮质激素治疗,但在筛选访视后停用环孢素。主要观察指标为输注期无葡萄膜炎发作(缓解)以及整个研究期无葡萄膜炎发作(持续缓解)。
13例患者纳入研究。在前治疗期发生了32次累及后段的葡萄膜炎发作。在输注期,4例患者(30.8%)无发作,9例患者共发生13次葡萄膜炎发作。其中10次发作(76.9%)发生在第14周或第22周。13例患者中有1例符合持续缓解的定义,其余12例患者在观察期共发生36次葡萄膜炎发作。输注期葡萄膜炎发作的平均次数和每日糖皮质激素剂量显著低于前治疗期或观察期。尽管英夫利昔单抗输注后视力有恢复的可能,但这种有益效果在第54周前未持续存在。所有患者均未发生严重不良事件。
本试验结果表明,英夫利昔单抗可有效抑制葡萄膜炎发作,具有糖皮质激素节省作用,对难治性白塞病葡萄膜炎患者的视力预后有积极影响。