Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland.
Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland.
Semin Arthritis Rheum. 2020 Feb;50(1):17-24. doi: 10.1016/j.semarthrit.2019.06.020. Epub 2019 Jun 28.
To compare treatment effectiveness in rheumatoid arthritis (RA) patients naïve to biological disease-modifying antirheumatic drugs (bDMARDs) treated with tocilizumab (TCZ) or TNF-inhibitor (TNFi) with (-combo) or without (-mono) conventional synthetic DMARDs (csDMARDs).
Patients with RA across 7 European registries, naïve to bDMARDs who initiated treatment with TCZ or TNFi from 2009 to 2016 were included. Drug retention rate was analyzed using Kaplan-Meier and Cox models, and CDAI over time by mixed models. The proportions of patients reaching CDAI low disease activity (LDA) and remission after one year were corrected for attrition.
6713 TNFi-combo, 3762 TNFi-mono, 646 TCZ-combo and 384 TCZ-mono were eligible. Crude median retention was 3.67 years (95%CI 3.41-3.83) for TNFi-combo, 4.14 (3.77-4.62) for TNFi-mono, 2.98 (2.76-3.34) for TCZ-combo and 3.63 years (3.34-5.03) for TCZ-mono. After adjustment for covariates, country and year of treatment initiation stratification, hazards of discontinuation were lower for TCZ-mono (0.60, 95% CI 0.52-0.69) and TCZ-combo (0.66, 95% CI 0.54-0.81) compared to TNFi-combo. Adjusted CDAI evolution was not significantly different between groups. CDAI LDA and remission corrected for attrition were similar between TCZ with or without csDMARDs and TNFi-combo.
In routine care across 7 European countries, the adjusted drug retention, adjusted CDAI over time and attrition-corrected response proportion for RA patients were similar for bio-naïve patients if treated with TNFi-combo, TCZ-combo or TCZ-mono.
比较初治生物改善病情抗风湿药(bDMARDs)的类风湿关节炎(RA)患者接受托珠单抗(TCZ)或肿瘤坏死因子抑制剂(TNFi)联合(- combo)或不联合(- mono)常规合成 DMARDs(csDMARDs)治疗的疗效。
纳入了 7 个欧洲登记处的初治 bDMARDs 的 RA 患者,他们在 2009 年至 2016 年间接受 TCZ 或 TNFi 治疗。使用 Kaplan-Meier 和 Cox 模型分析药物保留率,使用混合模型分析 CDAI 随时间的变化。经过流失校正后,比较了患者在一年后达到 CDAI 低疾病活动度(LDA)和缓解的比例。
共纳入 6713 例 TNFi-combo、3762 例 TNFi-mono、646 例 TCZ-combo 和 384 例 TCZ-mono。TNFi-combo、TNFi-mono、TCZ-combo 和 TCZ-mono 的未校正中位保留时间分别为 3.67 年(95%CI 3.41-3.83)、4.14 年(3.77-4.62)、2.98 年(2.76-3.34)和 3.63 年(3.34-5.03)。在调整协变量、治疗起始年份和国家分层后,与 TNFi-combo 相比,TCZ-mono(0.60,95%CI 0.52-0.69)和 TCZ-combo(0.66,95%CI 0.54-0.81)的停药风险较低。调整后的 CDAI 演变在各组之间无显著差异。经流失校正后,TCZ 联合或不联合 csDMARDs 与 TNFi-combo 相比,RA 患者达到 CDAI LDA 和缓解的比例相似。
在 7 个欧洲国家的常规治疗中,初治生物制剂的 RA 患者,如果接受 TNFi-combo、TCZ-combo 或 TCZ-mono 治疗,药物保留率、调整后的 CDAI 随时间的变化和经流失校正后的反应比例相似。