Jiang Aidou, Liu Ying, Wei Chunyan, Xiao Guirong
Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.
Front Pharmacol. 2025 Apr 28;16:1538563. doi: 10.3389/fphar.2025.1538563. eCollection 2025.
Eculizumab is expected to lead to increased susceptibility to infection. We performed a meta-analysis of data from randomized controlled trials (RCTs) to determine the risk of infection in eculizumab-treated patients.
We searched PubMed, EMBASE, Web of Science and ClinicalTrials.gov (up to 8 Oct 2024) to identify published RCTs that focused on the occurrence of infection in patients treated with eculizumab regardless of the indications of the patients. Relative risks and 95% confidence intervals (95% CIs) were calculated via the random effects model. (PROSPERO Code No. CRD42024562470).
Nine RCTs including 691 patients were eligible. Compared with the control (placebo or standard of care), eculizumab did not significantly increase the overall risk of infection (RR = 1.07; 95% CI, 0.89-1.28; = 44%), regardless of whether the infection was a general infection (RR = 1.07; 95% CI, 0.86-1.34; = 39%) or a serious infection (RR = 1.05; 95% CI, 0.75-1.47; = 11%). Analyses of subgroups revealed that eculizumab significantly increased the risk of general urinary system infection (RR = 1.33; 95% CI, 1.00-1.77; = 46%) and severe bacteremia (RR = 2.31; 95% CI, 1.04-5.13; = 0%).
Compared with placebo or standard of care, although eculizumab did not significantly increase the overall risk of infection, it was associated with 33% and 131% increases in the risk of general urinary system infection and severe bacteremia, respectively.
PROSPERO CRD42024562470.
依库珠单抗预计会导致感染易感性增加。我们对随机对照试验(RCT)的数据进行了荟萃分析,以确定接受依库珠单抗治疗的患者发生感染的风险。
我们检索了PubMed、EMBASE、科学网和ClinicalTrials.gov(截至2024年10月8日),以识别关注依库珠单抗治疗患者感染发生情况的已发表RCT,无论患者的适应症如何。通过随机效应模型计算相对风险和95%置信区间(95%CI)。(国际前瞻性系统评价注册编号:CRD42024562470)。
9项RCT(共691例患者)符合条件。与对照组(安慰剂或标准治疗)相比,依库珠单抗并未显著增加总体感染风险(风险比[RR]=1.07;95%CI为0.89-1.28;I²=44%),无论感染是普通感染(RR=1.07;95%CI为0.86-1.34;I²=39%)还是严重感染(RR=1.05;95%CI为0.75-1.47;I²=11%)。亚组分析显示,依库珠单抗显著增加了普通泌尿系统感染风险(RR=1.33;95%CI为1.00-1.77;I²=46%)和严重菌血症风险(RR=2.31;95%CI为1.04-5.13;I²=0%)。
与安慰剂或标准治疗相比,尽管依库珠单抗未显著增加总体感染风险,但它分别与普通泌尿系统感染风险增加33%和严重菌血症风险增加131%相关。
国际前瞻性系统评价注册编号CRD42024562470。