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口服C5a受体抑制剂阿伐考泮辅助治疗抗中性粒细胞胞浆抗体相关性血管炎患者。

Adjunctive Treatment With Avacopan, an Oral C5a Receptor Inhibitor, in Patients With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.

作者信息

Merkel Peter A, Niles John, Jimenez Richard, Spiera Robert F, Rovin Brad H, Bomback Andrew, Pagnoux Christian, Potarca Antonia, Schall Thomas J, Bekker Pirow

机构信息

University of Pennsylvania, Philadelphia.

Massachusetts General Hospital, Boston.

出版信息

ACR Open Rheumatol. 2020 Nov;2(11):662-671. doi: 10.1002/acr2.11185. Epub 2020 Oct 31.

Abstract

OBJECTIVE

This study aimed to evaluate the safety of avacopan, an orally administered C5a receptor inhibitor, for the treatment of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis in addition to standard-of-care (SOC) treatment with glucocorticoids with cyclophosphamide or rituximab.

METHODS

In this randomized 12-week study, twice daily avacopan (10 mg or 30 mg) plus SOC was assessed versus SOC only in patients with newly diagnosed/relapsing ANCA-associated vasculitis. Efficacy measurements included 50% or greater reduction in Birmingham Vasculitis Activity Score (BVAS) at day 85, rapid reduction (day 29) of BVAS to a score of 0 that was sustained through day 85, change in Vasculitis Damage Index (VDI), renal response (improvement in estimated glomerular filtration rate [eGFR], hematuria, and albuminuria), and health-related quality of life (HRQoL).

RESULTS

Forty-two patients were randomized (n = 13 SOC, n = 13 avacopan 10 mg, and n = 16 avacopan 30 mg). Serious adverse events occurred in 15% and 17% of patients receiving SOC only and patients receiving avacopan with SOC, respectively. In the intent-to-treat population, BVAS response was high across arms (11 of 13 SOC, 11 of 12 avacopan 10 mg, and 12 of 15 avacopan 30 mg); increases in mean VDI were greater with SOC only than with avacopan plus SOC (0.3 versus 0.1). Avacopan 30 mg was numerically superior to placebo and avacopan 10 mg in early remission (15%, 8%, and 20% for SOC only, avacopan 10 mg, and avacopan 30 mg, respectively), improved eGFR (+2.0 ml/min/1.73m , +1.3 ml/min/1.73m , and +6.2 ml/min/1.73m , respectively), renal response (17%, 40%, and 63%, respectively), and measures of HRQoL.

CONCLUSION

Avacopan in addition to SOC for ANCA-associated vasculitis was well tolerated, and at the higher study dose, it appeared to improve time to remission (ClinicalTrials.gov identifier NCT02222155).

摘要

目的

本研究旨在评估口服C5a受体抑制剂阿伐可泮联合糖皮质激素与环磷酰胺或利妥昔单抗的标准治疗(SOC)方案治疗抗中性粒细胞胞浆抗体(ANCA)相关血管炎的安全性。

方法

在这项为期12周的随机研究中,对新诊断/复发的ANCA相关血管炎患者,评估每日两次阿伐可泮(10毫克或30毫克)加SOC与单纯SOC的疗效。疗效指标包括第85天时伯明翰血管炎活动评分(BVAS)降低50%或更多、第29天时BVAS迅速降至0分并持续至第85天、血管炎损伤指数(VDI)变化、肾脏反应(估计肾小球滤过率[eGFR]、血尿和蛋白尿改善情况)以及健康相关生活质量(HRQoL)。

结果

42例患者被随机分组(13例接受单纯SOC,13例接受阿伐可泮10毫克,16例接受阿伐可泮30毫克)。接受单纯SOC和接受阿伐可泮联合SOC的患者中,严重不良事件发生率分别为15%和17%。在意向性治疗人群中,各治疗组的BVAS反应率都较高(单纯SOC组13例中有11例,阿伐可泮10毫克组12例中有11例,阿伐可泮30毫克组15例中有12例);单纯SOC组的平均VDI升高幅度大于阿伐可泮联合SOC组(分别为0.3和0.1)。阿伐可泮30毫克组在早期缓解方面在数值上优于安慰剂组和阿伐可泮10毫克组(单纯SOC组、阿伐可泮10毫克组和阿伐可泮30毫克组的缓解率分别为15%、8%和20%),改善eGFR方面(分别为+2.0毫升/分钟/1.73平方米、+1.3毫升/分钟/1.73平方米和+6.2毫升/分钟/1.73平方米)、肾脏反应方面(分别为17%、40%和63%)以及HRQoL指标方面均更优。

结论

阿伐可泮联合SOC治疗ANCA相关血管炎耐受性良好,在较高研究剂量下,似乎能改善缓解时间(ClinicalTrials.gov标识符NCT02222155)。

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