Zhou Qing, Zhou Yaodong, Chen Hao, Wang Zhen, Tang Zhibing, Liu Jinlian
Department of Orthopaedics, Suzhou Kowloon Hospital Affiliated to Shanghai Jiaotong University School of Medicine Jiangsu 215021, China.
Int J Clin Exp Med. 2014 Nov 15;7(11):3870-80. eCollection 2014.
Certolizumab pegol (CZP) is a novel anti-TNF agent that is used for patients with moderate to severe active rheumatoid arthritis (RA). However, the efficacy of CZP in RA remains controversial. Thus, we performed this meta-analysis to assess the efficacy and safety of CZP in the treatment of RA patients.
Eligible studies were randomized controlled trials (RCTs) that evaluated the efficacy and safe of CZP in the patients with active RA. The primary outcome was American College of Rheumatology 20% (ACR20), and secondary outcome were ACR50, ACR70, disease activity, patient-reported outcomes (PROs), and adverse events. A fixed-effect model or random-effect model was used to pool the estimates, depending on the absence or presence of heterogeneity among the included studies.
Nine RCTs with a total of 5228 patients were included in this meta-analysis, and all of the patients were administered CZP or placebo. The pooled results showed that CZP significantly improved the ACR20, ACR50, ACR70 response rates, and physical function. CZP was associated with a statistically significant reduction in Disease Activity Score in 28 joints-Erythrocyte sedimentation rate, arthritis pain, and fatigue. Patients who received CZP treatment did not have a higher incidence of treatment-related adverse events, no matter in any intensity.
CZP 200 or 400mg in the treatment of active RA significantly reduced the RA signs and symptoms, and improved physical function as compared with the placebo. More large-scale RCTs are needed to evaluate the long-term efficacy and safety of CZP in the treatment of active RA.
赛妥珠单抗(CZP)是一种新型抗肿瘤坏死因子(TNF)药物,用于治疗中重度活动性类风湿关节炎(RA)患者。然而,CZP在RA治疗中的疗效仍存在争议。因此,我们进行了这项荟萃分析,以评估CZP治疗RA患者的疗效和安全性。
纳入的研究为随机对照试验(RCT),评估了CZP在活动性RA患者中的疗效和安全性。主要结局指标为美国风湿病学会20%改善标准(ACR20),次要结局指标为ACR50、ACR70、疾病活动度、患者报告结局(PRO)及不良事件。根据纳入研究中是否存在异质性,采用固定效应模型或随机效应模型合并估计值。
本荟萃分析纳入了9项RCT,共5228例患者,所有患者均接受了CZP或安慰剂治疗。汇总结果显示,CZP显著提高了ACR20、ACR50、ACR70缓解率及身体功能。CZP与28个关节疾病活动评分-红细胞沉降率、关节炎疼痛及疲劳的显著降低相关。接受CZP治疗的患者无论在何种强度下,治疗相关不良事件的发生率均未更高。
与安慰剂相比,200或400mg的CZP治疗活动性RA可显著减轻RA体征和症状,并改善身体功能。需要更多大规模RCT来评估CZP治疗活动性RA的长期疗效和安全性。