Lee Y H, Bae S-C
Division of Rheumatology, Department of Internal Medicine, Korea University Anam Hospital, 73 Inchon-ro, 02841, Seoul, Korea.
Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea.
Z Rheumatol. 2017 Aug;76(6):528-534. doi: 10.1007/s00393-016-0133-z.
This study aimed to assess the relative efficacy and safety of certolizumab pegol (CZP) 200 and 400 mg + methotrexate (MTX) compared to placebo + MTX in patients with active rheumatoid arthritis (RA).
We performed a Bayesian network meta-analysis to combine the direct and indirect evidence from randomized controlled trials (RCTs) examining the efficacy and safety of CZP 200 and 400 mg + MTX and placebo + MTX (MTX group) in patients with active RA despite receiving MTX or a disease-modifying antirheumatic drug (DMARD).
Six RCTs (30349 patients) met the inclusion criteria. The ACR20 response rate was significantly higher in the CZP 200 and 400 mg + MTX group than in the MTX group (OR 7.30, 95 % credible interval [CrI] 3.31-16.92 and OR 5.48, 95 % CrI 2.98-10.30, respectively). CZP 400 mg + MTX tended to be more efficacious than CZP 200 mg + MTX (OR 1.33, 95 % CrI 0.61-2.97). A surface under the cumulative ranking curve (SUCRA)-based ranking probability indicated that CZP 400 mg + MTX had the highest probability of achieving the ACR20 response rate, followed by CZP 200 mg + MTX and MTX (SUCRA = 0.9007, 0.7156, and 0.0002, respectively). The ACR20, 50, and 70 response rate distributions were comparable. However, the safety based on the number of adverse event (AE)-related withdrawals did not differ significantly among the three interventions.
CZP, at dosages of 200 and 400 mg, in combination with MTX, was the efficacious intervention for active RA without causing a significant risk of AE-related withdrawals.
本研究旨在评估聚乙二醇化赛妥珠单抗(CZP)200mg和400mg联合甲氨蝶呤(MTX)与安慰剂联合MTX相比,在活动性类风湿关节炎(RA)患者中的相对疗效和安全性。
我们进行了一项贝叶斯网络荟萃分析,以整合来自随机对照试验(RCT)的直接和间接证据,这些试验考察了CZP 200mg和400mg联合MTX以及安慰剂联合MTX(MTX组)在尽管接受MTX或改善病情抗风湿药(DMARD)治疗但仍患有活动性RA的患者中的疗效和安全性。
六项RCT(30349例患者)符合纳入标准。CZP 200mg和400mg联合MTX组的美国风湿病学会(ACR)20缓解率显著高于MTX组(比值比[OR]分别为7.30,95%可信区间[CrI] 3.31 - 16.92;以及OR 5.48,95% CrI 2.98 - 10.30)。CZP 400mg联合MTX往往比CZP 200mg联合MTX更有效(OR 1.33,95% CrI 0.61 - 2.97)。基于累积排序曲线下面积(SUCRA)的排序概率表明,CZP 400mg联合MTX达到ACR20缓解率的概率最高,其次是CZP 200mg联合MTX和MTX(SUCRA分别为0.9007、0.7156和0.0002)。ACR20、50和70缓解率分布具有可比性。然而,基于不良事件(AE)相关撤药数量的安全性在三种干预措施之间没有显著差异。
200mg和400mg剂量的CZP联合MTX是治疗活动性RA的有效干预措施,且不会导致与AE相关撤药的显著风险。