Department of Rheumatology, Diakonhjemmet Hospital, PO Box 23 Vinderen, N-0319 Oslo, Norway.
Rheumatology (Oxford). 2012 Apr;51(4):670-8. doi: 10.1093/rheumatology/ker356. Epub 2011 Dec 9.
To compare baseline characteristics, responses and drug survival in patients with early RA starting SSZ or MTX in a real-life setting.
The analyses included DMARD-naïve patients with RA (disease duration ≤ 1 year) starting SSZ or MTX. Three- and 6-month effectiveness was compared by unadjusted analysis and with adjustment for propensity score quintile. In addition, effectiveness in SSZ- and MTX-treated patients matched for RF status and baseline DAS-28 was compared.
SSZ-treated patients (n = 175) had lower baseline disease activity than patients treated with MTX (n = 927) [mean 28-joint DAS (DAS-28) 4.4 vs 5.0, P < 0.001], and were less often RF positive (50 vs 61%, P = 0.006). Six-month mean ΔDAS-28 was smaller with SSZ than MTX (-1.0 vs -1.5, P = 0.003); the difference was not significant after adjustment for propensity score quintile (P = 0.36). For SSZ/MTX, 3-month ACR50 and European League Against Rheumatism (EULAR) good responses were 9/23% (P < 0.001) and 24/31% (P = 0.14), respectively. Three-year drug survival was superior for MTX (P < 0.001) and estimated 1-year survival rates were 42/75% for SSZ/MTX. In patients matched for baseline DAS-28 and RF, mean ΔDAS-28 (MTX -1.2, P = 0.55 vs SSZ) and EULAR good responses (39 vs 37%, P = 0.74) were similar at 6 months; drug survival was superior for MTX (P < 0.001).
Patients treated with SSZ as first DMARD were more often RF negative and had lower baseline disease activity. Drug survival was superior for MTX, and effectiveness was greater with MTX than with SSZ although the difference was reduced when adjusting for differences in baseline characteristics.
比较真实环境中起始应用 SSZ 或 MTX 的早期 RA 患者的基线特征、应答和药物生存情况。
分析纳入 DMARD 初治 RA(病程≤1 年)患者,起始应用 SSZ 或 MTX。采用未校正分析和倾向评分五分位调整比较 3 个月和 6 个月的疗效。此外,还比较了 RF 状态和基线 DAS-28 匹配的 SSZ 和 MTX 治疗患者的疗效。
SSZ 治疗患者(n=175)基线疾病活动度低于 MTX 治疗患者(n=927)[28 关节 DAS(DAS-28)均值 4.4 比 5.0,P<0.001],RF 阳性率较低(50%比 61%,P=0.006)。SSZ 治疗 6 个月时平均 DAS-28 降幅小于 MTX(-1.0 比-1.5,P=0.003);经倾向评分五分位调整后差异无统计学意义(P=0.36)。SSZ/MTX 治疗 3 个月 ACR50 和欧洲抗风湿病联盟(EULAR)良好反应率分别为 9/23%(P<0.001)和 24/31%(P=0.14)。MTX 的 3 年药物生存率较高(P<0.001),预计 SSZ/MTX 的 1 年生存率分别为 42/75%。在基线 DAS-28 和 RF 匹配的患者中,6 个月时 MTX 的平均 DAS-28 降幅(-1.2,P=0.55 比 SSZ)和 EULAR 良好反应率(39 比 37%,P=0.74)相似;MTX 的药物生存率较高(P<0.001)。
作为一线 DMARD 起始应用 SSZ 的患者 RF 阴性率更高且基线疾病活动度更低。MTX 的药物生存率较高,与 MTX 相比 SSZ 的疗效更好,尽管调整基线特征差异后,这种差异有所减小。