Author:
Kida Daihei,Takahashi Nobunori,Kaneko Atsushi,Hirano Yuji,Fujibayashi Takayoshi,Kanayama Yasuhide,Hanabayashi Masahiro,Yabe Yuichiro,Takagi Hideki,Oguchi Takeshi,Kato Takefumi,Funahashi Koji,Matsumoto Takuya,Ando Masahiko,Kuwatsuka Yachiyo,Tanaka Eiichi,Yasuoka Hidekata,Kaneko Yuko,Hirata Shintaro,Murakami Kosaku,Sobue Yasumori,Nishiume Tsuyoshi,Suzuki Mochihito,Yokota Yutaka,Terabe Kenya,Asai Shuji,Ishiguro Naoki,Kojima Toshihisa
Abstract
AbstractThis study aimed to evaluate the effectiveness of abatacept (ABA) by anti-cyclic citrullinated peptide (ACPA) status on disease activity as well as radiographic progression in patients with rheumatoid arthritis (RA) in clinical settings. A retrospective cohort study was conducted using data from a multicenter registry. Data from a total of 553 consecutive RA patients treated with intravenous ABA were included. We primarily compared the status of disease activity (SDAI) and radiographic progression (van der Heijde modified total Sharp score: mTSS) between the ACPA-negative (N = 107) and ACPA-positive (N = 446) groups. ‘ACPA positive’ was defined as ≥ 13.5 U/mL of anti-CCP antibody. Baseline characteristics between groups were similar. The proportion of patients who achieved low disease activity (LDA; SDAI ≤ 11) at 52 weeks was significantly higher in the ACPA-positive group. Multivariate logistic regression analysis identified ACPA positivity as an independent predictor for achievement of LDA at 52 weeks. Drug retention rate at 52 weeks estimated by the Kaplan–Meier curve was significantly higher in the ACPA-positive group. Achievement rate of structural remission (ΔmTSS ≤ 0.5) at 52 weeks was similar between groups. ABA treatment demonstrated a significantly higher clinical response and higher drug retention rate in ACPA-positive patients. Progression of joint destruction was similar between the ACPA-negative and ACPA-positive groups. Close attention should be paid to joint destruction even in patients showing a favorable response to ABA, especially when the ACPA status is positive.
Funder
Bristol-Myers Squibb and Ono Pharmaceutical CO., LTD.
Publisher
Springer Science and Business Media LLC