Cartin-Ceba Rodrigo, Golbin Jason M, Keogh Karina A, Peikert Tobias, Sánchez-Menéndez Marta, Ytterberg Steven R, Fervenza Fernando C, Specks Ulrich
Mayo Clinic, Rochester, Minnesota, USA.
Arthritis Rheum. 2012 Nov;64(11):3770-8. doi: 10.1002/art.34584.
This study was conducted to evaluate the efficacy and safety of repeated and prolonged B cell depletion with rituximab (RTX) for the maintenance of long-term remission in patients with chronic relapsing granulomatosis with polyangiitis (Wegener's) (GPA).
We conducted a single-center observational study of all patients with chronic relapsing GPA treated with at least 2 courses of RTX between January 1, 2000 and May 31, 2010. Participants in the Rituximab in ANCA-Associated Vasculitis (RAVE) trial were excluded from this analysis. Data were abstracted from electronic medical records.
Fifty-three patients with refractory GPA (median age 46 years [interquartile range (IQR) 30-61 years]; 53% women) received at least 2 courses of RTX to treat GPA relapses or to maintain remission. All but 1 patient had antineutrophil cytoplasmic antibodies (ANCA) against proteinase 3 (PR3). These patients received a median of 4 courses of RTX (IQR 3-5); all had depletion of B cells, and the median time to return of B cells was 8.5 months (IQR 6-11 months). All observed relapses occurred after reconstitution of B cells and were accompanied or preceded by an increase in ANCA levels, except for the 1 ANCA-negative patient. Infusion-related adverse events occurred in 16 patients. During the period of B cell depletion, 30 infections requiring antimicrobial therapy were recorded.
RTX appeared to be effective and safe for the induction and maintenance of remission in patients with chronic relapsing GPA. Repeated depletion of B lymphocytes seems to be associated with a low risk of infections. Preemptive re-treatment decisions can be individualized based on serial B lymphocyte and PR3 ANCA monitoring. The use of RTX for the maintenance of long-term remission merits further formal investigation.
本研究旨在评估利妥昔单抗(RTX)反复、长期清除B细胞对维持慢性复发性肉芽肿性多血管炎(韦格纳肉芽肿,GPA)患者长期缓解的疗效和安全性。
我们对2000年1月1日至2010年5月31日期间接受至少2个疗程RTX治疗的所有慢性复发性GPA患者进行了单中心观察性研究。抗中性粒细胞胞浆抗体相关血管炎(RAVE)试验的参与者被排除在本分析之外。数据从电子病历中提取。
53例难治性GPA患者(中位年龄46岁[四分位间距(IQR)30 - 61岁];53%为女性)接受至少2个疗程的RTX治疗以治疗GPA复发或维持缓解。除1例患者外,所有患者均有抗蛋白酶3(PR3)的抗中性粒细胞胞浆抗体(ANCA)。这些患者接受RTX的中位疗程为4个疗程(IQR 3 - 5);所有患者B细胞均被清除,B细胞恢复的中位时间为8.5个月(IQR 6 - 11个月)。除1例ANCA阴性患者外,所有观察到的复发均发生在B细胞重建后,且在复发之前或同时伴有ANCA水平升高。16例患者发生了与输注相关的不良事件。在B细胞清除期间,记录到30次需要抗菌治疗的感染。
RTX似乎对慢性复发性GPA患者诱导和维持缓解有效且安全。反复清除B淋巴细胞似乎与感染风险较低相关。可根据连续的B淋巴细胞和PR3 ANCA监测进行个体化的预防性再治疗决策。使用RTX维持长期缓解值得进一步进行正式研究。