Cleveland Clinic, Cleveland, Ohio.
Arthritis Rheumatol. 2014 Oct;66(10):2862-70. doi: 10.1002/art.38744.
To evaluate the efficacy and safety of rituximab (RTX) induction therapy and the duration of remission, when RTX is used with or without a conventional maintenance agent, in a cohort of patients with granulomatosis with polyangiitis (Wegener's) (GPA).
This was a retrospective, single-center study of patients with relapsing GPA treated with at least 1 course of RTX (4 weekly doses of 375 mg/m(2) intravenously [IV] or 2 fixed doses of 1,000 mg IV 2 weeks apart). Complete remission was defined as the absence of disease activity measured by a Birmingham Vasculitis Activity Score for Wegener's granulomatosis of 0 and not qualified by the prednisone dosage at the time.
Eighty-nine patients achieved remission after their first course of RTX and were not re-treated preemptively with RTX to maintain remission of their disease during followup. Among these patients, relapse-free survival was significantly higher in those who received a conventional maintenance agent (azathioprine, methotrexate, or mycophenolate mofetil) in conjunction with RTX and glucocorticoids (n = 47) than in those who received no additional immunosuppressive agent (n = 42) (P = 0.04). The hazard ratio of relapse in those receiving a maintenance agent was 0.53 (95% confidence interval 0.29-0.97). Serious adverse events did not differ between the 2 groups. Within a subset of 15 patients in the cohort who were relapse free 2 years after 1 course of RTX, remissions endured for 2-6 years in 8 patients.
RTX is an effective remission-inducing agent in GPA. The addition of a conventional maintenance agent to RTX and glucocorticoids decreased the incidence of relapse and did not result in a higher incidence of adverse events.
评估利妥昔单抗(RTX)诱导治疗的疗效和安全性,以及在复发性肉芽肿性多血管炎(韦格纳氏)(GPA)患者中使用或不使用常规维持药物时的缓解持续时间。
这是一项回顾性、单中心研究,纳入了至少接受过 1 个疗程 RTX(4 周剂量 375mg/m²静脉内[IV]或 2 周间隔 2 次固定剂量 1000mg IV)治疗的复发性 GPA 患者。完全缓解定义为无疾病活动,采用韦格纳氏肉芽肿伯明翰血管炎活动评分(Birmingham Vasculitis Activity Score for Wegener's granulomatosis)为 0,且当时无泼尼松剂量。
89 例患者在首次接受 RTX 治疗后达到缓解,且在随访期间未预防性地接受 RTX 再次治疗以维持疾病缓解。在这些患者中,与未接受额外免疫抑制剂(n = 42)相比,同时接受 RTX 和糖皮质激素以及常规维持药物(硫唑嘌呤、甲氨蝶呤或霉酚酸酯)治疗(n = 47)的患者无复发存活率显著更高(P = 0.04)。接受维持药物治疗的患者复发风险比为 0.53(95%置信区间 0.29-0.97)。两组的严重不良事件无差异。在队列中 15 例无复发生存 2 年的患者亚组中,8 例患者的缓解持续了 2-6 年。
RTX 是 GPA 诱导缓解的有效药物。RTX 联合糖皮质激素和常规维持药物可降低复发率,且不会增加不良事件发生率。