Interlandi Emanuela, Leccese Pietro, Olivieri Ignazio, Latanza Loredana
Uveitis and Ocular Immunopathology Unit, Department of Ophthalmology, "A. Cardarelli" Hospital of Naples, Italy.
Clin Exp Rheumatol. 2014 Jul-Aug;32(4 Suppl 84):S58-62. Epub 2014 Jul 8.
Behçet's disease (BD) is a chronic multisystem inflammatory disorder associated to uveitis that may represent a serious sight-threatening condition. The purpose of the present study is to assess the effectiveness of adalimumab as new strategic therapeutic approach in patients affected by severe Behçet's uveitis.
Clinical data from twelve selected patients (22 eyes) were retrospectively analysed. All patients received 40 mg of adalimumab subcutaneously, once every 2 weeks, in addition to traditional immunosuppressive on-going therapy and eight of them were switched to adalimumab after failure of infliximab therapy. Primary outcome measures included ocular inflammatory activity, frequency of uveitis attacks and steroid-sparing effect. Secondary outcomes were changes of best-corrected visual acuity (BCVA), impact on traditional immunosuppressive therapy and occurrence of adalimumab-related side effects.
Mean age of patients (11 males and 1 female) at the onset of disease was 24.34 years (±8.62 SD). Ocular involvement resulted bilateral in 83% of cases and mainly consisted in panuveitis (68% of eyes). After mean follow-up of 21 months (±9.63 SD) all patients but one (92%) achieved uveitis remission with BCVA improvement at least in one eye. Average uveitis attacks decreased from 2 to 0,42 during adalimumab (p<0.001) and daily-steroid dose was tapered in all adalimumab responders up to suspension in seven of them. No patient developed related side effects during adalimumab administration.
Our results demonstrate that adalimumab is a very effective and safe option for treatment of patients with severe and resistant Behçet's uveitis, providing an appropriate and long-term control of ocular inflammation.
白塞病(BD)是一种与葡萄膜炎相关的慢性多系统炎症性疾病,可能是一种严重威胁视力的疾病。本研究的目的是评估阿达木单抗作为重度白塞氏葡萄膜炎患者新的战略治疗方法的有效性。
回顾性分析了12例选定患者(22只眼)的临床资料。所有患者除接受传统免疫抑制持续治疗外,还每2周皮下注射40mg阿达木单抗,其中8例在英夫利昔单抗治疗失败后改用阿达木单抗。主要观察指标包括眼部炎症活动度、葡萄膜炎发作频率和激素节省效应。次要观察指标是最佳矫正视力(BCVA)的变化、对传统免疫抑制治疗的影响以及阿达木单抗相关副作用的发生情况。
患者(11例男性和1例女性)发病时的平均年龄为24.34岁(标准差±8.62)。83%的病例眼部受累为双侧,主要为全葡萄膜炎(68%的眼)。平均随访21个月(标准差±9.63)后,除1例患者外,所有患者(92%)均实现葡萄膜炎缓解,至少一只眼的BCVA有所改善。阿达木单抗治疗期间,葡萄膜炎平均发作次数从2次降至0.42次(p<0.001),所有对阿达木单抗有反应的患者每日激素剂量均逐渐减少,其中7例患者直至停用。在阿达木单抗给药期间,没有患者出现相关副作用。
我们的结果表明,阿达木单抗是治疗重度难治性白塞氏葡萄膜炎患者的一种非常有效且安全的选择,可对眼部炎症提供适当的长期控制。