Department of Rheumatology, Kakogawa Central City Hospital, 439, Honnmachi, Kakogawa-Cho, Kakogawa, Hyogo, 675-8611, Japan.
Department of Biophysics, Kobe University Graduate School of Health Sciences, Kobe, 654-0142, Japan.
Arthritis Res Ther. 2023 Jun 26;25(1):110. doi: 10.1186/s13075-023-03097-5.
To investigate the efficacy of mepolizumab in patients with eosinophilic granulomatosis with polyangiitis (EGPA) and factors contributing to glucocorticoid (GC) discontinuation.
We retrospectively studied EGPA patients treated with mepolizumab who were on GC at the time of induction of mepolizumab, at Japanese single center as of January 2023. Patients were classified into those who were able to discontinue GC at the time of the investigation (GC-free group) and those who continued (GC-continue group). Patient characteristics at the time of EGPA diagnosis (age, gender, absolute eosinophil counts, serum CRP level, serum IgE level, Rheumatoid factor (RF) / anti-neutrophil cytoplasmic antibody (ANCA) positivity, presence of asthma, affected organ, Five factor score (FFS), Birmingham Vasculitis Activity Score (BVAS) and characteristics at the time of mepolizumab induction (daily prednisolone dose, concomitant immunosuppressive maintenance therapy at the mepolizumab induction, prior history of GC pulse therapy, concomitant immunosuppressive therapy for remission induction,), history of relapse before mepolizumab induction and the duration of mepolizumab treatment were compared. We also followed the clinical indicators (absolute eosinophil counts, CRP and IgE levels, BVAS, Vascular Damage Index (VDI)) and daily prednisolone dosage at the EGPA diagnosis, at the mepolizumab induction and at the survey.
Twenty-seven patients were included in the study. At the time of the study, patients had received mepolizumab for median 31 months (IQR, 26 to 40), the daily prednisolone dose was median 1 mg (IQR, 0 to 1.8) and GC-free was achieved in 13 patients (48%). Among clinical indicators that have improved by conventional therapy before the induction of mepolizumab, eosinophil counts, GC doses and BVAS have successively shown significant reductions throughout the observation period both GC-free and GC-continue. Of the GC-free patients, 7 were ANCA positive and 12 had FFS1 or more. Univariate analysis showed that the absolute eosinophil counts at diagnosis was significantly higher in the GC-free group (median 8165/µl (IQR, 5138 to 13,409) vs. 4360/µl (IQR, 151 to 8380), P = 0.037) and significantly fewer patients presented with gastrointestinal lesions (2 (15%) vs. 8 (57%), P = 0.025), while multivariate analysis showed no significant differences. Mepolizumab treatment significantly improved VDI in the GC-continue group (P = 0.004).
After three years of treatment with mepolizumab, approximately 50% of patients with EGPA achieved GC-free status. GC could be discontinued even in severe cases and ANCA-positive cases. Although multivariate analysis did not extract any significant factors contributing to achieving GC-free, we found that improvement in eosinophil counts and BVAS led to GC reduction, resulted in protection of organ damages in both the GC-free and continuation groups. The significance of achieving GC-free remission in EGPA patients was demonstrated.
探讨美泊利珠单抗治疗嗜酸性肉芽肿性多血管炎(EGPA)患者的疗效,以及导致糖皮质激素(GC)停药的因素。
我们回顾性研究了截至 2023 年 1 月在日本单中心接受美泊利珠单抗治疗且诱导治疗时正在接受 GC 治疗的 EGPA 患者。患者分为能够在调查时停用 GC(GC 停药组)和继续使用 GC(GC 继续组)的患者。在 EGPA 诊断时(年龄、性别、绝对嗜酸性粒细胞计数、血清 CRP 水平、血清 IgE 水平、类风湿因子(RF)/抗中性粒细胞胞浆抗体(ANCA)阳性、哮喘存在、受累器官、五因子评分(FFS)、Birmingham 血管炎活动评分(BVAS))和诱导美泊利珠单抗时(每日泼尼松剂量、诱导美泊利珠单抗时同时使用免疫抑制维持治疗、GC 脉冲治疗史、缓解诱导时同时使用免疫抑制治疗)的患者特征进行比较。我们还比较了诱导美泊利珠单抗前、EGPA 诊断时、诱导美泊利珠单抗时和调查时的临床指标(绝对嗜酸性粒细胞计数、CRP 和 IgE 水平、BVAS、血管损伤指数(VDI))和每日泼尼松剂量。
研究纳入 27 例患者。研究时,患者接受美泊利珠单抗治疗的中位时间为 31 个月(IQR,26 至 40),每日泼尼松剂量为 1 毫克(IQR,0 至 1.8),13 例(48%)患者达到 GC 停药。在接受美泊利珠单抗诱导治疗前通过常规治疗改善的临床指标中,嗜酸性粒细胞计数、GC 剂量和 BVAS 在观察期间均逐渐降低,无论是 GC 停药组还是 GC 继续组。在 GC 停药组中,7 例为 ANCA 阳性,12 例为 FFS1 或更高。单因素分析显示,GC 停药组的诊断时绝对嗜酸性粒细胞计数明显更高(中位数 8165/µl(IQR,5138 至 13409)与 4360/µl(IQR,151 至 8380),P=0.037),胃肠道病变患者明显较少(2(15%)与 8(57%),P=0.025),而多因素分析未显示出显著差异。美泊利珠单抗治疗可显著改善 GC 继续组的 VDI(P=0.004)。
经过三年的美泊利珠单抗治疗,大约 50%的 EGPA 患者达到 GC 停药状态。即使在严重病例和 ANCA 阳性病例中,也可以停用 GC。虽然多因素分析未提取出任何导致 GC 停药的显著因素,但我们发现嗜酸性粒细胞计数和 BVAS 的改善导致 GC 减少,从而在 GC 停药和继续组中均保护了器官损伤。证明了在 EGPA 患者中实现 GC 缓解的重要性。