Mount Sinai Hospital, Joseph and Wolf Lebovic Building, Second Floor, Room 2-006, 60 Murray Street, Toronto, Ontario M5G 1X5.
J Rheumatol. 2011 Jun;38(6):990-6. doi: 10.3899/jrheum.100935. Epub 2011 Mar 1.
To assess the kinetics of response to certolizumab pegol (CZP), and association between rapid response and longterm outcomes, in patients with active rheumatoid arthritis (RA).
This was a post-hoc analysis of the randomized, double-blind RAPID 1 study in patients who received methotrexate (MTX) and either CZP 200 mg subcutaneously or placebo every 2 weeks for 52 weeks. Clinical and radiographic outcomes at Week 52 were evaluated based on the Disease Activity Score 28 (DAS28) ≥ 1.2 and American College of Rheumatology 20% (ACR20) responses at Week 6 and Week 12.
Clinical responses [European League Against Rheumatism (EULAR), DAS28 ≥ 1.2, and ACR20 responses] were rapid in CZP-treated patients. Week 12 DAS28 ≥ 1.2 responders had better clinical and radiographic outcomes at Week 52 compared with nonresponders. Among Week 12 responders, incremental benefit of earlier response was observed: Week 6 DAS28 ≥ 1.2 responders and ACR20 responders had significantly higher ACR response rates and were more likely to achieve remission at Week 52 than Week 12 responders. Patients with a clinical response at Week 6 had faster, more meaningful sustained improvements in patient-derived outcomes than those responding by Week 12 only.
Rapid attainment of clinical response in patients with RA is associated with improved longterm outcomes. Analysis of the kinetics of response to CZP during the first 12 weeks of therapy potentially permits informed prediction of clinical success or need to alter treatment. In patients not achieving a clinical response at Week 12 treatment adjustment should be considered. Trial registration NCT00152386.
评估活性类风湿关节炎(RA)患者接受培塞利珠单抗(CZP)治疗的应答动力学,以及快速应答与长期结局的相关性。
这是一项针对接受甲氨蝶呤(MTX)治疗的患者的随机、双盲 RAPID 1 研究的事后分析,这些患者每 2 周皮下注射 200mg CZP 或安慰剂,共 52 周。根据第 6 周和第 12 周的疾病活动评分 28(DAS28)≥1.2 和美国风湿病学会 20%(ACR20)应答,评估第 52 周的临床和放射学结局。
CZP 治疗患者的临床应答(欧洲抗风湿病联盟(EULAR)、DAS28≥1.2 和 ACR20 应答)迅速。第 12 周 DAS28≥1.2 应答者在第 52 周的临床和放射学结局优于无应答者。在第 12 周的应答者中,更早应答的获益递增:第 6 周 DAS28≥1.2 应答者和 ACR20 应答者在第 52 周的 ACR 应答率更高,更有可能达到缓解。在第 6 周有临床应答的患者比仅在第 12 周有应答的患者在患者报告结局方面更快、更有意义地持续改善。
RA 患者快速达到临床应答与改善长期结局相关。对治疗前 12 周 CZP 应答动力学的分析可能有助于预测临床成功或需要改变治疗。对于在第 12 周未达到临床应答的患者,应考虑调整治疗。临床试验注册号 NCT00152386。