Takanashi Satoshi, Kondo Yasushi, Saito Shuntaro, Kikuchi Jun, Hanaoka Hironari, Takeuchi Tsutomu, Kaneko Yuko
Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Int J Rheum Dis. 2023 Nov;26(11):2240-2247. doi: 10.1111/1756-185X.14920. Epub 2023 Sep 13.
To elucidate the efficacy and safety of rituximab in special types of rheumatoid arthritis.
We retrospectively reviewed all patients with rheumatoid arthritis with lymphoproliferative disorder or vasculitis treated with rituximab between April 2010 and June 2022 at Keio University Hospital. We assessed the effectiveness of rituximab using the Disease Activity Score for 28 joints-erythrocyte sedimentation rate (DAS28-ESR), Clinical Disease Activity Index (CDAI), and safety of rituximab during the disease course. We also assessed the glucocorticoid-sparing effects of rituximab.
We included eight patients with a history of lymphoproliferative disorder and five patients with rheumatoid vasculitis. They were treated with rituximab without high-dose glucocorticoid. The mean DAS28-ESR and CDAI scores significantly improved 12 months after rituximab administration (DAS28-ESR, 4.7 vs. 2.7, p < .001; CDAI, 16.0 vs. 5.1, p = .006, respectively), and the dose of prednisolone was reduced from a mean of 7.4 mg/day to 4.0 mg/day at 12 months (p = .05) and 3.2 mg/day at the last visit (p = .04). During the mean follow-up period of 52 months, we recorded one recurrence of lymphoproliferative disorder (not B-cell type) in patients with a history of lymphoproliferative disorder and remarkable improvement of skin ulcers in patients with vasculitis.
B-cell depletion by rituximab may be a useful treatment option for patients with lymphoproliferative disorder and rheumatoid vasculitis.
阐明利妥昔单抗在特殊类型类风湿关节炎中的疗效和安全性。
我们回顾性分析了2010年4月至2022年6月在庆应义塾大学医院接受利妥昔单抗治疗的所有患有类风湿关节炎合并淋巴增殖性疾病或血管炎的患者。我们使用28个关节疾病活动评分-红细胞沉降率(DAS28-ESR)、临床疾病活动指数(CDAI)评估利妥昔单抗的有效性,并评估疾病过程中利妥昔单抗的安全性。我们还评估了利妥昔单抗的糖皮质激素节省效应。
我们纳入了8例有淋巴增殖性疾病病史的患者和5例类风湿血管炎患者。他们接受了利妥昔单抗治疗,未使用大剂量糖皮质激素。利妥昔单抗给药12个月后,平均DAS28-ESR和CDAI评分显著改善(DAS28-ESR,4.7对2.7,p<0.001;CDAI,16.0对5.1,p = 0.006),泼尼松龙剂量在12个月时从平均7.4毫克/天降至4.0毫克/天(p = 0.05),在最后一次随访时降至3.2毫克/天(p = 0.04)。在平均52个月的随访期内,我们记录到1例有淋巴增殖性疾病病史的患者出现淋巴增殖性疾病复发(非B细胞型),血管炎患者的皮肤溃疡有显著改善。
利妥昔单抗清除B细胞可能是治疗淋巴增殖性疾病和类风湿血管炎患者的一种有效治疗选择。