Department of Rheumatology, University Hospital of North Norway, Post Box 14, 9038 Tromsø, Norway.
Rheumatology (Oxford). 2013 Nov;52(11):2041-7. doi: 10.1093/rheumatology/ket257. Epub 2013 Aug 11.
Rituximab (RTX) is an anti-CD20 antibody used successfully in granulomatosis with polyangiitis (GPA) for induction and maintenance of remission. Our study aims to evaluate the long-term efficacy and safety of chronic pre-emptive RTX therapy in GPA.
Retrospective study of 35 GPA patients treated with RTX between April 2004 and September 2011 for active disease and maintenance. RTX was initiated as two 1 g infusions 2 weeks apart and thereafter 2 g of RTX was readministered annually. Patients were followed for 47 (2-88) months. They received a median RTX dose of 8 g (2-13) over 5 (1-10) rounds.
All patients had a clinical response, but nine relapses were recorded (flare rate of 6.6/100 patient-years). At last visit, 13 patients (37%) had discontinued RTX mainly due to hypogammaglobulinaemia (57%). Nine patients (26%) had severe infections (infection rate of 6.6/100 patient-years) and 10 patients (29%) had chronic infections. Risks factors for severe infections are a high cumulative dose of CYC, low CD4 cell count and a significant drop in total immunoglobulins after the first RTX round. Risks factors for chronic infections are low IgG level during RTX maintenance and possibly the cumulative RTX dose.
Long-term pre-emptive RTX maintenance was efficacious in reducing the risk for relapse but was discontinued in one-third of the patients. The patients' net state of immunodeficiency under RTX changes over time as low immunoglobulin serum levels increased the risk for infections.
利妥昔单抗(RTX)是一种抗 CD20 抗体,已成功用于肉芽肿性多血管炎(GPA)的诱导和缓解维持。本研究旨在评估慢性预防性 RTX 治疗 GPA 的长期疗效和安全性。
回顾性研究了 2004 年 4 月至 2011 年 9 月期间因活动期疾病和维持治疗而接受 RTX 治疗的 35 例 GPA 患者。RTX 起始剂量为每 2 周输注 1g,共 2 次,此后每年输注 2g。患者随访 47(2-88)个月。中位 RTX 剂量为 8g(2-13),共 5(1-10)个疗程。
所有患者均有临床反应,但有 9 例复发(复发率为 6.6/100 患者年)。末次随访时,13 例患者(37%)因低丙种球蛋白血症(57%)停用 RTX。9 例患者(26%)发生严重感染(感染率为 6.6/100 患者年),10 例患者(29%)发生慢性感染。严重感染的危险因素是 CYC 的累积剂量高、CD4 细胞计数低和首次 RTX 治疗后总免疫球蛋白显著下降。慢性感染的危险因素是 RTX 维持期间 IgG 水平低,可能还有累积 RTX 剂量。
长期预防性 RTX 维持治疗可降低复发风险,但三分之一的患者停药。随着血清低免疫球蛋白水平增加感染风险,RTX 下患者的免疫缺陷净状态随时间而变化。