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一项比较甲氨蝶呤和霉酚酸酯治疗非感染性葡萄膜炎的随机临床试验。

A randomized clinical trial comparing methotrexate and mycophenolate mofetil for noninfectious uveitis.

作者信息

Rathinam Sivakumar R, Babu Manohar, Thundikandy Radhika, Kanakath Anuradha, Nardone Natalie, Esterberg Elizabeth, Lee Salena M, Enanoria Wayne T A, Porco Travis C, Browne Erica N, Weinrib Rachel, Acharya Nisha R

机构信息

Aravind Eye Care System, Madurai, India.

Aravind Eye Care System, Coimbatore, India.

出版信息

Ophthalmology. 2014 Oct;121(10):1863-70. doi: 10.1016/j.ophtha.2014.04.023. Epub 2014 Jun 7.

Abstract

OBJECTIVE

To compare the relative effectiveness of methotrexate and mycophenolate mofetil for noninfectious intermediate uveitis, posterior uveitis, or panuveitis.

DESIGN

Multicenter, block-randomized, observer-masked clinical trial.

PARTICIPANTS

Eighty patients with noninfectious intermediate, posterior, or panuveitis requiring corticosteroid-sparing therapy at Aravind Eye Hospitals in Madurai and Coimbatore, India.

INTERVENTION

Patients were randomized to receive 25 mg weekly oral methotrexate or 1 g twice daily oral mycophenolate mofetil and were monitored monthly for 6 months. Oral prednisone and topical corticosteroids were tapered.

MAIN OUTCOME MEASURES

Masked examiners assessed the primary outcome of treatment success, defined by achieving the following at 5 and 6 months: (1) ≤0.5+ anterior chamber cells, ≤0.5+ vitreous cells, ≤0.5+ vitreous haze and no active retinal/choroidal lesions in both eyes, (2) ≤10 mg of prednisone and ≤2 drops of prednisolone acetate 1% a day, and (3) no declaration of treatment failure because of intolerability or safety. Additional outcomes included time to sustained corticosteroid-sparing control of inflammation, change in best spectacle-corrected visual acuity, resolution of macular edema, adverse events, subgroup analysis by anatomic location, and medication adherence.

RESULTS

Forty-one patients were randomized to methotrexate and 39 to mycophenolate mofetil. A total of 67 patients (35 methotrexate, 32 mycophenolate mofetil) contributed to the primary outcome. Sixty-nine percent of patients achieved treatment success with methotrexate and 47% with mycophenolate mofetil (P = 0.09). Treatment failure from adverse events or tolerability was not different by treatment arm (P = 0.99). There were no differences between treatment groups in time to corticosteroid-sparing control of inflammation (P = 0.44), change in best spectacle-corrected visual acuity (P = 0.68), or resolution of macular edema (P = 0.31).

CONCLUSIONS

There was no statistically significant difference in corticosteroid-sparing control of inflammation between patients receiving methotrexate or mycophenolate mofetil. However, there was a 22% difference in treatment success favoring methotrexate.

摘要

目的

比较甲氨蝶呤和霉酚酸酯治疗非感染性中间葡萄膜炎、后葡萄膜炎或全葡萄膜炎的相对疗效。

设计

多中心、区组随机、观察者盲法临床试验。

参与者

印度马杜赖和哥印拜陀的阿拉文德眼科医院80例需要减少糖皮质激素用量治疗的非感染性中间、后或全葡萄膜炎患者。

干预

患者随机接受每周25mg口服甲氨蝶呤或每日2次每次1g口服霉酚酸酯,并每月监测6个月。口服泼尼松和局部用糖皮质激素逐渐减量。

主要观察指标

盲法检查者评估治疗成功的主要结局,定义为在5个月和6个月时达到以下标准:(1)双眼前房细胞≤0.5+、玻璃体细胞≤0.5+、玻璃体混浊≤0.5+且无活动性视网膜/脉络膜病变;(2)泼尼松≤10mg且醋酸泼尼松龙1%滴眼液每日≤2滴;(3)未因不耐受或安全性宣告治疗失败。其他结局包括持续减少糖皮质激素用量控制炎症的时间、最佳矫正视力变化、黄斑水肿消退情况、不良事件、按解剖部位进行亚组分析以及药物依从性。

结果

41例患者随机接受甲氨蝶呤治疗,39例接受霉酚酸酯治疗。共有67例患者(35例甲氨蝶呤组,32例霉酚酸酯组)纳入主要结局分析。甲氨蝶呤组69%的患者治疗成功,霉酚酸酯组为47%(P = 0.09)。各治疗组因不良事件或耐受性导致的治疗失败无差异(P = 0.99)。治疗组间在减少糖皮质激素用量控制炎症的时间(P = 0.44)、最佳矫正视力变化(P = 0.68)或黄斑水肿消退情况(P = 0.31)方面无差异。

结论

接受甲氨蝶呤或霉酚酸酯治疗的患者在减少糖皮质激素用量控制炎症方面无统计学显著差异。然而,甲氨蝶呤组治疗成功率高22%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3d6/4177935/ca18c85a343f/nihms604187f1.jpg

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