Cacciapaglia Fabio, Venerito Vincenzo, Stano Stefano, Fornaro Marco, Lopalco Giuseppe, Iannone Florenzo
Rheumatology Unit, Department of Emergency and Organs Transplantation (DETO), University of Bari, 70124 Bari, Puglia, Italy.
J Pers Med. 2022 Feb 25;12(3):353. doi: 10.3390/jpm12030353.
Few studies compared adalimumab to other targeted therapies in head-to-head randomized clinical trials (RCTs) for rheumatoid arthritis (RA), but multiple comparisons are not available. This Bayesian Network Meta-Analysis evaluated which targeted therapy is more likely to achieve ACR50 response with good safety at 24 weeks of treatment in RA. A systematic literature review was conducted for head-to-head phase 3 RCTs that compared adalimumab to other targeted therapies in combination with methotrexate (MTX) or as monotherapy to treat RA patients, and searched through MEDLINE, EMBASE, Cochrane Library and Clinicaltrial.gov. The outcomes of interest were ACR50 response and withdrawals due to adverse events at 24 weeks. WinBUGS 1.4 software (MRC Biostatistics Unit, Cambridge, UK) was used to perform the analyses, using a random effect model. Sixteen studies were included in the analysis. The most favorable SUCRA for the ACR50 response rate at 24 weeks of treatment in combination with MTX was ranked by upadacitinib, followed by baricitinib, tofacitinib and filgotinib. As monotherapy, the highest probability was ranked by tocilizumab followed by sarilumab. No significant differences in safety profile among treatment options were found. Jak-inhibitors in combination with MTX and interleukin-6 antagonism as monotherapy showed the highest probability to achieve ACR50 response after 24 weeks of treatment. None of assessed targeted therapies were associated to risk of withdrawal due to adverse events. Key messages: Direct and indirect comparison between adalimumab and other targeted therapies demonstrated some differences in terms of efficacy that may help to drive RA treatment. Jak-inhibitors and interleukine-6 antagonists ranked as first in the probability to achieve ACR50 response after 24 weeks of treatment in combination with methotrexate or monotherapy, respectively.
在类风湿关节炎(RA)的头对头随机临床试验(RCT)中,很少有研究将阿达木单抗与其他靶向治疗进行比较,且无法进行多项比较。这项贝叶斯网络荟萃分析评估了哪种靶向治疗在RA治疗24周时更有可能实现ACR50反应且安全性良好。对阿达木单抗与其他靶向治疗联合甲氨蝶呤(MTX)或作为单药治疗RA患者的头对头3期RCT进行了系统的文献综述,并通过MEDLINE、EMBASE、Cochrane图书馆和Clinicaltrial.gov进行检索。感兴趣的结局是24周时的ACR50反应和因不良事件导致的撤药情况。使用WinBUGS 1.4软件(英国剑桥医学研究委员会生物统计学部)采用随机效应模型进行分析。16项研究纳入分析。在联合MTX治疗24周时,对于ACR50反应率,最有利的SUCRA排名是乌帕替尼,其次是巴瑞替尼、托法替布和非戈替尼。作为单药治疗,概率最高的是托珠单抗,其次是萨瑞鲁单抗。在各治疗方案之间未发现安全性方面的显著差异。与MTX联合使用的Jak抑制剂和作为单药治疗的白细胞介素-6拮抗剂在治疗24周后实现ACR50反应的概率最高。没有评估的靶向治疗与因不良事件导致撤药的风险相关。关键信息:阿达木单抗与其他靶向治疗之间的直接和间接比较在疗效方面显示出一些差异,这可能有助于推动RA治疗。Jak抑制剂和白细胞介素-6拮抗剂分别在联合甲氨蝶呤或单药治疗24周后实现ACR50反应的概率方面排名第一。