Department of Rheumatology, Swedish Medical Center, Seattle, Washington, USA
University of Washington, Seattle, Washington, USA.
RMD Open. 2024 Jan 31;10(1):e003423. doi: 10.1136/rmdopen-2023-003423.
An important consideration in the treatment of patients with psoriatic arthritis (PsA) is whether the addition of methotrexate (MTX) to biologics has greater efficacy than biologic monotherapy with respect to efficacy outcomes in these patients.
To conduct a network meta-analysis (NMA) comparing biologics by treatment class with and without MTX for treatment of adults with active PsA.
A systematic literature review (SLR) identified randomised, double-blinded, controlled trials, and a Bayesian NMA compared biologics with and without MTX by treatment class (tumour necrosis factor inhibitors (TNFi), interleukin-23 inhibitors (IL-23i) and IL-17i). Efficacy outcomes included American College of Rheumatology 20%, 50% and 70% (ACR20, ACR50 and ACR70) improvement response.
The SLR initially identified 31 studies, of which 17 met feasibility criteria for the NMA by containing the 'without MTX' subgroup. For ACR20 efficacy (the most robust assessment examined), all active treatments were significantly better than placebo. No statistically significant differences were demonstrated between biologic monotherapy (for all classes examined) and biologics in combination with MTX for ACR20/50. IL-17i were comparable to IL-23i, and IL-17i were significantly better than TNFi for ACR20. Although limited by fewer trials, TNFi, IL-23i and IL-17i were not statistically different for ACR50/70.
Concomitant use of MTX and biologics did not improve ACR efficacy outcomes versus biologic monotherapy. MTX does not appear to be necessary as a background therapy when biologics are used for the achievement of ACR20/50 responses in patients with PsA.
在治疗银屑病关节炎(PsA)患者时,一个重要的考虑因素是,与生物制剂单药治疗相比,甲氨蝶呤(MTX)联合生物制剂治疗在这些患者的疗效结局方面是否更有效。
通过网络荟萃分析(NMA)比较不同治疗类别的生物制剂与 MTX 联合或不联合治疗成人活动性 PsA 的疗效。
系统文献检索(SLR)确定了随机、双盲、对照试验,贝叶斯 NMA 比较了生物制剂与 MTX 联合或不联合治疗的疗效,治疗类别包括肿瘤坏死因子抑制剂(TNFi)、白细胞介素-23 抑制剂(IL-23i)和白细胞介素-17 抑制剂(IL-17i)。疗效结局包括美国风湿病学会 20%、50%和 70%(ACR20、ACR50 和 ACR70)改善反应。
SLR 最初确定了 31 项研究,其中 17 项研究通过包含“无 MTX”亚组符合 NMA 的可行性标准。对于 ACR20 疗效(评估最稳健的指标),所有活性治疗均显著优于安慰剂。生物制剂单药治疗(所有研究类别)与 MTX 联合生物制剂治疗在 ACR20/50 方面均无统计学差异。IL-17i 与 IL-23i 相当,IL-17i 对 ACR20 的疗效明显优于 TNFi。虽然试验数量较少,但 TNFi、IL-23i 和 IL-17i 在 ACR50/70 方面无统计学差异。
与生物制剂单药治疗相比,MTX 联合生物制剂并未改善 ACR 疗效结局。当生物制剂用于实现 PsA 患者的 ACR20/50 反应时,MTX 似乎不需要作为背景治疗。