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评估利妥昔单抗在 75 岁及以上抗中性粒细胞胞质抗体相关性血管炎患者诱导缓解和维持治疗中的作用。

Evaluation of Rituximab for Induction and Maintenance Therapy in Patients 75 Years and Older With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.

机构信息

Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.

Department of Geriatrics, Sorbonne Université, Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Pitié-Salpêtrière-Charles Foix, Paris, France.

出版信息

JAMA Netw Open. 2022 Jul 1;5(7):e2220925. doi: 10.1001/jamanetworkopen.2022.20925.

Abstract

IMPORTANCE

Older patients are underrepresented in studies of rituximab for the treatment of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Little is known about outcomes and adverse events associated with the use of rituximab therapy among patients 75 years and older with ANCA-associated vasculitis.

OBJECTIVE

To examine outcomes and adverse events associated with the use of rituximab therapy in patients 75 years and older with ANCA-associated vasculitis, specifically granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA).

DESIGN, SETTING, AND PARTICIPANTS: This multicenter cohort study involved 93 patients 75 years and older with ANCA-associated vasculitis from 36 university and nonuniversity hospitals in France. Data were obtained from the French Vasculitis Study Group database between January 1, 2000, and July 1, 2018, and a call for observation sent to French Vasculitis Study Group members on June 6, 2019. Data analysis was performed from November 15 to December 31, 2021. Inclusion criteria included a diagnosis of GPA or MPA according to European Medicines Agency classification criteria and receipt of treatment with rituximab after age 75 years. Patients were excluded if they were missing relevant clinical or biological data. Data on race and ethnicity were not reported because inclusion of this information was not authorized by the ethics committee.

EXPOSURE

At least 1 infusion of rituximab as induction or maintenance therapy.

MAIN OUTCOMES AND MEASURES

Occurrence of remission, relapse, drug discontinuation, death, and serious infections (including types of serious infections).

RESULTS

Of 238 patients screened, 93 were included (median [IQR] age, 79.4 [76.7-83.1] years; 51 women [54.8%]); 52 patients (55.9%) had a diagnosis of GPA, and 41 (44.1%) had a diagnosis of MPA. Thirty patients (32.3%) received rituximab as induction therapy in combination with high-dose glucocorticoid regimens, 27 (29.0%) received rituximab as maintenance therapy, and 36 (38.7%) received rituximab as both induction and maintenance therapy. The median (IQR) follow-up was 2.3 (1.1-4.0) years. Among 66 patients who received rituximab as induction therapy, 57 (86.4%) achieved remission, and 2 (3.0%) experienced relapses. The incidence of serious infection was significantly higher when rituximab was used as induction therapy vs maintenance therapy (46.6 [95% CI, 24.8-79.7] per 100 patient-years vs 8.4 [95% CI, 3.8-15.9] per 100 patient-years; P = .004). Most infections (12 of 22 [54.5%]) were gram-negative bacterial infections. The incidence of death was 19.7 (95% CI, 7.2-42.9) per 100 patient-years among those who received rituximab as induction therapy and 5.3 (95% CI, 1.9-11.6) per 100 patient-years among those who received rituximab as maintenance therapy.

CONCLUSIONS AND RELEVANCE

In this cohort study, rituximab therapy was associated with achievement and maintenance of remission in most patients 75 years and older with ANCA-associated vasculitis. The incidence of serious infections and death was high when rituximab was used as induction therapy in combination with high-dose glucocorticoid regimens but not when rituximab was used as maintenance therapy. Efforts might focus on reducing serious infections during the first months of therapy.

摘要

重要性:在研究利妥昔单抗治疗抗中性粒细胞胞浆抗体(ANCA)相关性血管炎的疗效时,年龄较大的患者代表性不足。对于 75 岁及以上的 ANCA 相关性血管炎患者使用利妥昔单抗治疗的结果和不良事件知之甚少,尤其是对于肉芽肿性多血管炎(GPA)或显微镜下多血管炎(MPA)患者。

目的:研究 75 岁及以上的 GPA 或 MPA 患者使用利妥昔单抗治疗的结果和不良事件。

设计、地点和参与者:这项多中心队列研究纳入了来自法国 36 所大学和非大学医院的 93 名 75 岁及以上的 GPA 或 MPA 患者。数据来自 2000 年 1 月 1 日至 2018 年 7 月 1 日期间的法国血管炎研究组数据库,并于 2019 年 6 月 6 日向法国血管炎研究组成员发出了观察请求。数据分析于 2021 年 11 月 15 日至 12 月 31 日进行。纳入标准包括符合欧洲药品管理局分类标准的 GPA 或 MPA 诊断和 75 岁后接受利妥昔单抗治疗。如果患者缺失相关临床或生物学数据,则被排除在外。种族和民族数据未报告,因为伦理委员会不授权纳入这些信息。

暴露因素:至少 1 次利妥昔单抗输注作为诱导或维持治疗。

主要结果和措施:缓解、复发、药物停药、死亡和严重感染(包括严重感染类型)的发生。

结果:在筛选的 238 名患者中,有 93 名患者被纳入(中位[IQR]年龄,79.4[76.7-83.1]岁;51 名女性[54.8%]);52 名患者(55.9%)诊断为 GPA,41 名患者(44.1%)诊断为 MPA。30 名患者(32.3%)接受利妥昔单抗联合大剂量糖皮质激素方案作为诱导治疗,27 名患者(29.0%)接受利妥昔单抗作为维持治疗,36 名患者(38.7%)接受利妥昔单抗作为诱导和维持治疗。中位(IQR)随访时间为 2.3(1.1-4.0)年。在 66 名接受利妥昔单抗诱导治疗的患者中,57 名(86.4%)达到缓解,2 名(3.0%)复发。严重感染的发生率在利妥昔单抗作为诱导治疗与维持治疗时显著更高(每 100 名患者年发生率分别为 46.6[95%CI,24.8-79.7]和 8.4[95%CI,3.8-15.9];P = .004)。大多数感染(22 例中的 12 例[54.5%])为革兰氏阴性菌感染。接受利妥昔单抗诱导治疗的患者中,死亡发生率为每 100 名患者年 19.7(95%CI,7.2-42.9),而接受利妥昔单抗维持治疗的患者中,死亡发生率为每 100 名患者年 5.3(95%CI,1.9-11.6)。

结论和相关性:在这项队列研究中,75 岁及以上的 GPA 或 MPA 患者使用利妥昔单抗治疗与缓解和缓解维持相关。当利妥昔单抗与大剂量糖皮质激素方案联合使用作为诱导治疗时,严重感染和死亡的发生率较高,但当利妥昔单抗作为维持治疗时,其发生率并不高。治疗的最初几个月内可能需要努力降低严重感染的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb6/9270693/f17bc143cb05/jamanetwopen-e2220925-g001.jpg

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