Vassilopoulos Athanasios, Vassilopoulos Stephanos, Kalligeros Markos, Shehadeh Fadi, Mylonakis Eleftherios
Infectious Diseases Division, Rhode Island Hospital, Providence, RI, United States.
Warren Alpert Medical School of Brown University, Providence, RI, United States.
Front Med (Lausanne). 2023 Mar 1;10:1110548. doi: 10.3389/fmed.2023.1110548. eCollection 2023.
Rituximab and azathioprine are used to induce or maintain remission in patients with ANCA-associated vasculitis (AAV). We evaluated the incidence of serious infections and infection-related deaths in patients with AAV treated with rituximab and azathioprine, during the maintenance of remission period.
We searched PubMed and EMBASE for randomized clinical trials (RCTs) and observational studies evaluating immunosuppressive agents in patients with AAV. We defined serious or severe infections according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. The study was registered on PROSPERO (CRD42022366269).
From 1,265 abstracts, we identified 21 studies (7 RCTs and 14 observational), with relevant data. We included data from 1,284 and 2,938 individuals for assessment in our primary and secondary outcomes, respectively. The overall cumulative incidence of serious infections was 15.99% (CI 95%: 6.95-27.53%) during the total follow-up period (induction and maintenance) and 7.62% (CI 95%: 4.43-11.43%) during the maintenance period. Additionally, we found a 0.49% overall case fatality rate (CI 95%: 0.02-1.37%) and a 0.09% infection-related mortality rate (CI 95%: 0.00-0.51%) during maintenance treatment. Notably, we found a 14.61% (CI 95%: 10.19-19.61%) cumulative incidence of serious infections among patients who received rituximab and a 5.93% (CI 95%: 1.19-13.26%) cumulative incidence of serious infections among patients who received azathioprine during maintenance. Moreover, the cumulative incidence of serious infections during the total follow-up period (induction and maintenance) was 20.81% (CI 95%:4.56-43.70%) for the combination of cyclophosphamide and azathioprine and 14.12% (CI 95%: 5.20-26.00%) for rituximab.
The cumulative incidence of serious infections during total follow-up and maintenance was within expected limits, while fatal infections during maintenance treatment were uncommon. Additionally, treatment with rituximab for both induction and maintenance did not exceed the anticipated by previous studies incidence of serious infections. Clinical practice and long-term follow up data are needed to corroborate these findings.
Identifier: PROSPERO (CRD42022366269).
利妥昔单抗和硫唑嘌呤用于诱导或维持抗中性粒细胞胞浆抗体相关性血管炎(AAV)患者的缓解。我们评估了在缓解维持期接受利妥昔单抗和硫唑嘌呤治疗的AAV患者中严重感染及感染相关死亡的发生率。
我们检索了PubMed和EMBASE,以查找评估AAV患者免疫抑制剂的随机临床试验(RCT)和观察性研究。我们根据美国国立癌症研究所不良事件通用术语标准(CTCAE)第5.0版定义严重或重度感染。该研究已在国际前瞻性系统评价注册库(PROSPERO,注册号:CRD42022366269)注册。
从1265篇摘要中,我们确定了21项研究(7项RCT和14项观察性研究)并获取了相关数据。我们分别纳入了1284例和2938例个体的数据用于主要和次要结局的评估。在整个随访期(诱导期和维持期),严重感染的总体累积发生率为15.99%(95%CI:6.95 - 27.53%),在维持期为7.62%(95%CI:4.43 - 11.43%)。此外,在维持治疗期间,我们发现总体病死率为0.49%(95%CI:0.02 - 1.37%),感染相关死亡率为0.09%(95%CI:0.00 - 0.51%)。值得注意的是,在维持期接受利妥昔单抗治疗的患者中,严重感染的累积发生率为14.61%(95%CI:10.19 - 19.61%),接受硫唑嘌呤治疗的患者中为5.93%(95%CI:1.19 - 13.26%)。此外,在整个随访期(诱导期和维持期),环磷酰胺和硫唑嘌呤联合治疗的严重感染累积发生率为20.81%(95%CI:4.56 - 43.70%),利妥昔单抗治疗为14.12%(95%CI:5.20 - 26.00%)。
整个随访期和维持期严重感染的累积发生率在预期范围内,而维持治疗期间致命感染并不常见。此外,利妥昔单抗用于诱导和维持治疗的严重感染发生率未超过先前研究预期。需要临床实践和长期随访数据来证实这些发现。
标识符:PROSPERO(CRD42022366269)