Song Yeo-Jin, Cho Soo-Kyung, Choi Se Rim, Lee Shin-Seok, Lee Hye-Soon, Park Sung-Hoon, Lee Yeon-Ah, Park Min-Chan, Kim Hyoun-Ah, Lee Soo-Bin, Park Ha-Rim, Nam Eunwoo, Sung Yoon-Kyoung
Hanyang University Institute for Rheumatology Research, Seoul, Korea.
Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea.
Korean J Intern Med. 2025 Sep;40(5):835-844. doi: 10.3904/kjim.2024.344. Epub 2025 Aug 29.
BACKGROUND/AIMS: To identify factors associated with achieving low disease activity (LDA) after 48 weeks of targeted therapy in patients with rheumatoid arthritis (RA) despite not meeting treat-to-target (T2T) criteria at week 24.
Data were collected from a multicenter, prospective observational cohort of Korea patients with RA receiving targeted therapy between April 2020 and July 2023. Patients who continued their initial targeted therapy despite not achieving LDA at week 24 were assigned to the LDA and non-LDA groups at week 48. Multivariable logistic regression was employed to identify factors associated with achieving delayed LDA at week 48.
Among 456 patients with RA receiving targeted therapy, 213 were included in the analysis: 96 and 117 in the LDA and non-LDA groups, respectively. Patients with more comorbidities (HR 0.40, 95% CI 0.22-0.73) and those with seropositive RA (HR 0.15, 95% CI 0.03-0.70) were less likely to achieve LDA at week 48. Conversely, significant reductions in DAS28-ESR (HR 2.42, 95% CI 1.27-4.60) and HAQ-DI (HR 2.70, 95% CI 1.46-5.01) from enrolment to week 24, along with the absence of non-steroidal anti-inflammatory drug (NSAID) use at week 24 (HR 2.15, 95% CI 1.06-4.38), were associated with a greater likelihood of achieving delayed LDA at week 48.
Many patients with RA can achieve delayed LDA with continued targeted therapy without adhering to the T2T strategy. Key factors include fewer comorbidities, seronegative RA, substantial disease activity reduction in the first 24 weeks, and stopping NSAID at week 24.
背景/目的:确定类风湿关节炎(RA)患者在接受靶向治疗48周后达到低疾病活动度(LDA)的相关因素,尽管这些患者在第24周未达到治疗目标(T2T)标准。
数据收集自2020年4月至2023年7月期间接受靶向治疗的韩国RA患者的多中心前瞻性观察队列。在第24周未达到LDA但继续接受初始靶向治疗的患者在第48周被分为LDA组和非LDA组。采用多变量逻辑回归来确定与在第48周实现延迟LDA相关的因素。
在456例接受靶向治疗的RA患者中,213例纳入分析:LDA组和非LDA组分别为96例和117例。合并症较多的患者(HR 0.40,95%CI 0.22 - 0.73)和血清学阳性的RA患者(HR 0.15,95%CI 0.03 - 0.70)在第48周达到LDA的可能性较小。相反,从入组到第24周DAS28 - ESR(HR 2.42,95%CI 1.27 - 4.60)和HAQ - DI(HR 2.70,95%CI 1.46 - 5.01)显著降低,以及在第24周未使用非甾体抗炎药(NSAID)(HR 2.15,95%CI 1.06 - 4.38),与在第48周实现延迟LDA的可能性更大相关。
许多RA患者在不遵循T2T策略的情况下,通过持续的靶向治疗可以实现延迟LDA。关键因素包括合并症较少、血清学阴性RA、在最初24周内疾病活动度大幅降低以及在第24周停用NSAID。