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霉酚酸酯联合他克莫司治疗狼疮性肾炎。

Combination therapy of mycophenolate mofetil and tacrolimus in lupus nephritis.

机构信息

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Lupus. 2010 Jul;19(8):935-40. doi: 10.1177/0961203310365714. Epub 2010 Apr 13.

DOI:10.1177/0961203310365714
PMID:20388722
Abstract

Since most lupus nephritis patients have an incomplete response to mycophenolate mofetil, combination regimens may improve outcomes. Tacrolimus (FK506) has shown some benefit in lupus nephritis in small trials, and combined with mycophenolate mofetil is standard immunosuppression in transplant patients. We investigate the addition of FK506 to mycophenolate mofetil, in patients who were mycophenolate mofetil failures. All patients were part of a prospective cohort, but evaluated retrospectively. Seven lupus nephritis patients (mean age 27.1, 100% female, 42% Caucasian and 42% African American) were evaluated. Three patients had combined ISN class III and V, two ISN class IV, one ISN class V and II and one ISN class IV and V. Six were taking an ACE-inhibitor or angiotensin receptor blocker, 6 hydroxychloroquine and 5 prednisone (mean dose 11.5 mg; range 0-30 mg). Mean mycophenolate mofetil dose at time of tacrolimus addition was 2.8 g (range 2-3 g). Mean tacrolimus dose was 3.4 mg (range 2-8 mg) titrated to a mean level of 4.67 ng/dl (range 2.2-11.8 ng/dl) for a mean of duration of 16 months (range 2-54 months). Two patients continued both therapies, while five discontinued therapy. One patient achieved a complete renal remission, while three achieved partial remission with 82.9%, 77.1%, 55.3% reductions in proteinuria. Toxicity limited the use of combination therapy: diabetic ketoacidosis (one patient), pneumonia (two) and muscle pain (two). These data suggest that adding tacrolimus in patients refractory to mycophenolate mofetil might have some benefit, although complete responses were rare. Unfortunately, tacrolimus toxicity appeared to be prevalent in these systemic lupus erythematosus patients, limiting its long term use.

摘要

由于大多数狼疮肾炎患者对吗替麦考酚酯的反应不完全,联合治疗方案可能会改善结局。他克莫司(FK506)在小型试验中显示对狼疮肾炎有一定益处,并且与吗替麦考酚酯联合使用是移植患者的标准免疫抑制方案。我们研究了在吗替麦考酚酯治疗失败的患者中添加 FK506。所有患者均为前瞻性队列的一部分,但进行了回顾性评估。评估了 7 例狼疮肾炎患者(平均年龄 27.1 岁,100%为女性,42%为白种人,42%为非裔美国人)。3 例患者同时患有 ISN Ⅲ和Ⅴ型,2 例患有 ISN Ⅳ型,1 例患有 ISN Ⅴ和Ⅱ型,1 例患有 ISN Ⅳ和Ⅴ型。6 例患者服用血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂,6 例服用羟氯喹,5 例服用泼尼松(平均剂量 11.5mg;范围 0-30mg)。添加他克莫司时吗替麦考酚酯的平均剂量为 2.8g(范围 2-3g)。平均他克莫司剂量为 3.4mg(范围 2-8mg),调整至平均浓度 4.67ng/dl(范围 2.2-11.8ng/dl),平均治疗时间为 16 个月(范围 2-54 个月)。2 例患者继续使用两种药物治疗,而 5 例患者停用治疗。1 例患者获得完全肾脏缓解,3 例患者蛋白尿减少 82.9%、77.1%和 55.3%,获得部分缓解。毒性限制了联合治疗的使用:糖尿病酮症酸中毒(1 例)、肺炎(2 例)和肌肉疼痛(2 例)。这些数据表明,在对吗替麦考酚酯耐药的患者中添加他克莫司可能会有一定的益处,尽管完全缓解很少见。不幸的是,他克莫司毒性似乎在这些系统性红斑狼疮患者中普遍存在,限制了其长期使用。

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