TY - JOUR
T1 - Selection of treatment regimens based on shared decision-making in patients with rheumatoid arthritis on remission in the FREE-J study
AU - Tanaka, Yoshiya
AU - Yamaguchi, Ayako
AU - Miyamoto, Toshiaki
AU - Tanimura, Kazuhide
AU - Iwai, Hideyuki
AU - Kaneko, Yuko
AU - Takeuchi, Tsutomu
AU - Amano, Koichi
AU - Iwamoto, Naoki
AU - Kawakami, Atsushi
AU - Murakami, Miho
AU - Nishimoto, Norihiro
AU - Atsumi, Tatsuya
AU - Sumida, Takayuki
AU - Ohmura, Koichiro
AU - Mimori, Tsuneyo
AU - Yamanaka, Hisashi
AU - Fujio, Keishi
AU - Fujino, Yoshihisa
AU - Saito, Kazuyoshi
AU - Nakano, Kazuhisa
AU - Hirata, Shintaro
AU - Nakayamada, Shingo
N1 - Funding Information:
This work was supported in part by a Grant-In-Aid for Japan Agency for Medical Research and Development [#15ek0410016h0002].
Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press on behalf of the British Society for Rheumatology.
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Objective: To compare the outcome of various treatment de-escalation regimens in patients with RA who achieved sustained remission. Methods: At period 1, 436 RA patients who were treated with MTX and bDMARDs and had maintained DAS28(ESR) at <2.6 were divided into five groups based on shared patient/physician decision-making; continuation, dose reduction and discontinuation of MTX or bDMARDs. At end of year 1, patients who achieved DAS28(ESR) <3.2 were allowed to enrol in period 2 for treatment using the de-escalation regimens for another year. The primary and secondary endpoints were the proportion of patients with DAS28(ESR) <2.6 at year 1 and 2, respectively. Results: Based on shared decision-making, 81.4% elected de-escalation of treatment and 48.4% selected de-escalation of MTX. At end of period 1, similar proportions of patients maintained DAS28(ESR) <2.6 (continuation, 85.2%; MTX dose reduction, 79.0%; MTX-discontinuation, 80.0%; bDMARD dose reduction, 73.9%), although the rate was significantly different between the continuation and bDMARD-discontinuation. At end of period 2, similar proportions of patients of the MTX groups maintained DAS28(ESR) <2.6 (continuation or de-escalation), but the rates were significantly lower in the bDMARD-discontinuation group. However, half of the latter group satisfactorily discontinued bDMARDs. Adverse events were numerically lower in MTX and bDMARD-de-escalation groups during period 1 and 2, compared with the continuation group. Conclusions: After achieving sustained remission by combination treatment of MTX/bDMARDs, disease control was achieved comparably by continuation, dose reduction or discontinuation of MTX and dose reduction of bDMARDs at end of year 1. Subsequent de-escalation of MTX had no impacts on disease control but decreased adverse events in year 2.
AB - Objective: To compare the outcome of various treatment de-escalation regimens in patients with RA who achieved sustained remission. Methods: At period 1, 436 RA patients who were treated with MTX and bDMARDs and had maintained DAS28(ESR) at <2.6 were divided into five groups based on shared patient/physician decision-making; continuation, dose reduction and discontinuation of MTX or bDMARDs. At end of year 1, patients who achieved DAS28(ESR) <3.2 were allowed to enrol in period 2 for treatment using the de-escalation regimens for another year. The primary and secondary endpoints were the proportion of patients with DAS28(ESR) <2.6 at year 1 and 2, respectively. Results: Based on shared decision-making, 81.4% elected de-escalation of treatment and 48.4% selected de-escalation of MTX. At end of period 1, similar proportions of patients maintained DAS28(ESR) <2.6 (continuation, 85.2%; MTX dose reduction, 79.0%; MTX-discontinuation, 80.0%; bDMARD dose reduction, 73.9%), although the rate was significantly different between the continuation and bDMARD-discontinuation. At end of period 2, similar proportions of patients of the MTX groups maintained DAS28(ESR) <2.6 (continuation or de-escalation), but the rates were significantly lower in the bDMARD-discontinuation group. However, half of the latter group satisfactorily discontinued bDMARDs. Adverse events were numerically lower in MTX and bDMARD-de-escalation groups during period 1 and 2, compared with the continuation group. Conclusions: After achieving sustained remission by combination treatment of MTX/bDMARDs, disease control was achieved comparably by continuation, dose reduction or discontinuation of MTX and dose reduction of bDMARDs at end of year 1. Subsequent de-escalation of MTX had no impacts on disease control but decreased adverse events in year 2.
KW - DMARD
KW - biologics
KW - remission
KW - rheumatoid arthritis
KW - treatment
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UR - http://www.scopus.com/inward/citedby.url?scp=85140626176&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/keac075
DO - 10.1093/rheumatology/keac075
M3 - Article
C2 - 35136990
AN - SCOPUS:85140626176
SN - 1462-0324
VL - 61
SP - 4273
EP - 4285
JO - Rheumatology and Rehabilitation
JF - Rheumatology and Rehabilitation
IS - 11
ER -