Karolinska University Hospital, Solna, Stockholm, Sweden.
Lupus. 2014 Mar;23(3):299-304. doi: 10.1177/0961203313519158. Epub 2014 Jan 7.
Mycophenolate mofetil (MMF) is used off-label for systemic lupus erythematosus (SLE) and systemic vasculitis. The study aim was to investigate clinical use and treatment results with MMF in patients with SLE and systemic vasculitis. This study included patients with SLE or systemic vasculitis with ongoing or previous MMF treatment. Data on treatment outcome were obtained through medical record reviews. A total of 135 of 648 (21%) patients with SLE and 43 of 455 (9%) patients with systemic vasculitis had ongoing or previous MMF treatment. Among SLE patients, the most common organ manifestation at baseline (treatment start) was renal involvement (50%). Most of the systemic vasculitis patients had Wegener's granulomatosis (GPA) (65%). Median dose of MMF was 2000 mg/day. Glucocorticoid (GC) doses were significantly reduced during MMF treatment from 21.7 mg/day at baseline to 8.3 mg/day at 12 months (p < 0.05). Forty-six percent of the patients were good responders after 12 months. The most common adverse events (AES) leading to discontinuation were side effects in the gastrointestinal tract (40%) and general side effects (30%). "Survival-on-drug" analysis suggested that 40% of the patients remained on long-term MMF treatment. In conclusion, MMF was used in 21% of the SLE patients and 9% of the systemic vasculitis patients. MMF appeared to be effective with a reasonable survival-on-drug and a GC-sparing effect.
霉酚酸酯(MMF)被用于治疗红斑狼疮(SLE)和系统性血管炎等疾病。本研究旨在调查 MMF 在 SLE 和系统性血管炎患者中的临床应用和治疗效果。该研究纳入了正在接受或曾接受过 MMF 治疗的 SLE 或系统性血管炎患者。通过病历回顾获取治疗结局数据。648 例 SLE 患者中有 135 例(21%)、455 例系统性血管炎患者中有 43 例(9%)正在接受或曾接受过 MMF 治疗。SLE 患者的基线(治疗开始时)最常见的器官表现是肾脏受累(50%)。大多数系统性血管炎患者患有韦格纳肉芽肿病(GPA)(65%)。MMF 的中位剂量为 2000mg/天。在 MMF 治疗期间,GC 剂量从基线时的 21.7mg/天显著减少到 12 个月时的 8.3mg/天(p<0.05)。46%的患者在 12 个月后成为良好反应者。导致停药的最常见不良事件(AES)是胃肠道副作用(40%)和一般副作用(30%)。“药物持续生存”分析表明,40%的患者长期接受 MMF 治疗。总之,MMF 被用于 21%的 SLE 患者和 9%的系统性血管炎患者。MMF 似乎有效,具有合理的药物持续生存和 GC 节省效应。