Jansen Jeroen P, Buckley Felicity, Dejonckheere Fred, Ogale Sarika
Mapi Group, 180 Canal Street, Suite 503, Boston, MA 02114, USA.
Health Qual Life Outcomes. 2014 Jul 3;12:102. doi: 10.1186/1477-7525-12-102.
To compare biologics as monotherapy or in combination with methotrexate (MTX) in terms of patient reported outcomes (PROs) in RA patients with an inadequate response to conventional DMARDs (DMARD-IR).
With a systematic literature review 17 RCTs were identified that evaluated adalimumab, certolizumab pegol, etanercept, golimumab, infliximab, abatacept, anakinra or tocilizumab. Treatment effects in terms of pain (0-100 mm), patient's global assessment of disease activity (PGA; 0-100 mm), Health Assessment-Questionnaire (HAQ) disability index (DI; 0-3), and the physical component summary (PCS) of the SF36 Health Survey (0-100) at 24 weeks were combined by means of Bayesian network meta-analyses.
With tocilizumab monotherapy, greater improvements in pain (difference = -11.1; (95% Credible Interval -21.3, -0.1)) and PGA (-10.3 (-20.4, 0.8)) were observed than with aTNF monotherapy. Tocilizumab was at least as efficacious as aTNF in HAQ-DI improvements (-0.16; (-0.37, 0.05)). aTNF + MTX (-17.9 (-23.1, -13.0) & -19.1 (-24.2, -14.4)), abatacept + MTX (-23.0 (-47.3, 1. 5) & -13.6 (-28.4, 2.0)) and tocilizumab + MTX (-16.0 (-26.3, -6.3) & -15.1 (-25.1, -5.7)) showed comparable reductions in pain and PGA relative to MTX. Efficacy of anakinra + MTX was much smaller as compared to other biologics. The greatest improvements in HAQ-DI relative to MTX were observed with aTNF + MTX (-0.30 (-0.37, -0.22)) and tocilizumab + MTX (-0.27 (-0.42, -0.12)), followed by abatacept + MTX (-0.21 (-0.37, -0.05)) and anakinra + MTX (-0.11 (-0.26, 0.05)). The improvements in SF36-PCS with abatacept + MTX, aTNF + MTX and tocilizumab + MTX were comparable. There is a >90% probability that aTNF + MTX results in a greater improvement in pain (-12.4), PGA (-16.1) and HAQ-DI (-0.21) than aTNF as monotherapy. Efficacy of tocilizumab + MTX showed comparable improvements in PROs as tocilizumab monotherapy.
Based on a network meta-analysis involving indirect comparison of trial findings, the following observations were made for DMARD-IR patients. In monotherapy, tocilizumab was associated with a greater improvement in pain and self-reported disease activity than aTNF, and was at least as efficacious regarding functional ability. The improvements in PROs with aTNF, abatacept and tocilizumab in combination with MTX were comparable. Improvements in PROs with tocilizumab as monotherapy were similar to that of tocilizumab + MTX, whereas aTNF as monotherapy was likely to be less efficacious than aTNF + MTX.
比较生物制剂单药治疗或与甲氨蝶呤(MTX)联合治疗对传统改善病情抗风湿药治疗反应不足(DMARD-IR)的类风湿关节炎(RA)患者的患者报告结局(PROs)的影响。
通过系统文献综述,确定了17项随机对照试验(RCT),这些试验评估了阿达木单抗、聚乙二醇化赛妥珠单抗、依那西普、戈利木单抗、英夫利昔单抗、阿巴西普、阿那白滞素或托珠单抗。通过贝叶斯网络荟萃分析,综合了24周时疼痛(0-100mm)、患者对疾病活动的整体评估(PGA;0-100mm)、健康评估问卷(HAQ)残疾指数(DI;0-3)以及SF36健康调查的身体成分总结(PCS,0-100)方面的治疗效果。
与肿瘤坏死因子(TNF)单药治疗相比,托珠单抗单药治疗在疼痛(差异=-11.1;(95%可信区间-21.3,-0.1))和PGA(-10.3(-20.4,0.8))方面有更大改善。在HAQ-DI改善方面(-0.16;(-0.37,0.05)),托珠单抗至少与TNF单药治疗同样有效。TNF+MTX(-17.9(-23.1,-13.0)和-19.1(-24.2,-14.4))、阿巴西普+MTX(-23.0(-47.3,1.5)和-13.6(-28.4,2.0))以及托珠单抗+MTX(-16.0(-26.3,-6.3)和-15.1(-25.1,-5.7))在疼痛和PGA方面相对于MTX有类似程度的降低。与其他生物制剂相比,阿那白滞素+MTX的疗效要小得多。相对于MTX,在HAQ-DI方面改善最大的是TNF+MTX(-0.30(-0.37,-0.22))和托珠单抗+MTX(-0.27(-0.42,-0.12)),其次是阿巴西普+MTX(-0.21(-0.37,-0.05))和阿那白滞素+MTX(-0.11(-0.26,0.05))。阿巴西普+MTX、TNF+MTX和托珠单抗+MTX在SF36-PCS方面的改善相当。TNF+MTX在疼痛(-12.4)、PGA(-16.1)和HAQ-DI(-0.21)方面比TNF单药治疗有更大改善的概率大于90%。托珠单抗+MTX在PROs方面的疗效与托珠单抗单药治疗相当。
基于涉及试验结果间接比较的网络荟萃分析,对DMARD-IR患者有以下观察结果。在单药治疗中,托珠单抗在疼痛和自我报告的疾病活动方面比TNF有更大改善,并且在功能能力方面至少同样有效。TNF、阿巴西普和托珠单抗与MTX联合治疗在PROs方面的改善相当。托珠单抗单药治疗在PROs方面的改善与托珠单抗+MTX相似,而TNF单药治疗可能比TNF+MTX疗效更差。