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. 2020 Feb 7;79(6):744–759. doi: 10.1136/annrheumdis-2019-216656

Table 5.

Primary outcomes of studies investigating csDMARD, bDMARD and tsDMARD tapering and stopping

Study Primary outcome Endpoint (week) Treatment arm N Result P value
csDMARD tapering
Kaeley 2016 (MUSICA)107 Mean DAS28-CRP 24 ADA 40 mg Q2W+7.5 mg MTX 154 4.12 0.014
ADA 40 mg Q2W+20 mg MTX 155 3.75
Keystone 2016 (CAMEO)144 ΔDAS28-ESR 24 ETN 50 mg QW; MTX discontinuation 98 0.5 0.815
ETN 50 mg QW +MTX continuation 107 0.04
Pope EULAR 2017/ACR 2018/2019108–110 ΔDAS28-ESR 76 CZP +csDMARD continuation 37 −2.1 NR
CZP +csDMARD discontinuation 44 −2.1
Burmester ACR 2018 (SEMIRA)111 ΔDAS28-ESR 24 TCZ ±csDMARDs; GC tapering 131 0.538 <0.001
TCZ ±csDMARDs; GC continuation 128 −0.075
Pablos 2018 (JUST-ACT)112 ΔDAS28-ESR week 16 week 28 28 TCZ 8 mg/kg+MTX 82 0.007 95% CI −0.40 to 0.27
TCZ 8 mg/kg+PLC 82 0.073
Kremer 2018 (COMP-ACT)113 ΔDAS28-ESR week 24 week 40 40 TCZ 162 mg s.c. +PLC 147 0.46 95% CI 0.045 to 0.592
TCZ 162 mg s.c. +MTX 147 0.14
Edwards 2018 (ACT-TAPER)114 Pat. Maintaining EULAR good/moderate response from week 24–60 60 TCZ 8 mg/kg Q4W+PBO 136 77% 0.036
TCZ 8 mg/kg Q4W+MTX 136 65%
Stouten 2018 (CareRA)115 116 DAS28-CRP <2.6 65 MTX +LEF->MTX 15 mg/week 32 94% 0.031
MTX+LEF->LEF 20 mg/day 26 73%
bDMARD tapering
Oba 2017/Tanaka ACR 2018 (RRRR)140 141 1-year sustained discontinuation rate of INF 106 INF 3 mg/8 mg/10 mg/kg Q8W based on TNF levels 170 24% 0.631
INF standard 3 mg/kg Q8W 167 21%
Chatzidionysiou 2016 (ADMIRE)142 DAS28 <2.6 at week 28 28 ADA +MTX continuation 16 94% 0.001
ADA discontinuation; MTX monotherapy 16 33%
Ghiti Moghadam 2016/2018 (POET)117 118 % of pat. DAS28 ≥3.2 + ΔDAS28 >0.6 for 1 year 52 Stopping TNFi 531 51% <0.001
Continuation of TNFi 286 18%
Atsumi 2017 (C-OPERA)119 ΔmTSS 104 CZP +MTX continuation 108 0.66 0.001
Stopping CZP; MTX+PLC 71 3.01
Kaneko 2018 (SURPRISE)121 TCZ free rate 104 stopping TCZ; MTX monotherapy 49 67% 0.001
stopping TCZ; No DMARD 53 29%
Weinblatt 2017 (C-EARLY)120 DAS28-ESR ≤3.2 without flares during week 52–104 104 CZP 200 mg Q2W+MTX (standard) 84 49% Reference
CZP 200 mg Q4W+MTX (reduced frequency) 126 53% 0.112
Placebo +MTX (CZP stopped) 79 39% 0.041
Ibrahim 2017 (OPTIRRA)122 Flare rate (ΔDAS28 ≥0.6 + DAS28 >3.2 + ΔSJC OR ΔDAS28 >1.2 + DAS28 >3.2) 24 TNFi 33% tapering; csDMARD 26 12% 0.873
TNFi 66% tapering; csDMARD 21 29% 0.097
Control; csDMARD continuation 50 16% Reference
Bouman 2017 (DRESS)145 Incidence of major flare (ΔDAS28-CRP >1.2 or ΔDAS28-CRP >0.6+DAS28-CRP ≥3.2 for >12 weeks) 144 TNFi dose reduction extension 115 17% 3%, 95% CI -10% to 15%
Usual care extension 57 14%
l’Ami 2018124 ∆DAS28-ESR 28 ADA 40 mg Q3W±MTX 27 −0.14 0.01
ADA 40 mg Q2W±MTX 27 0.3
tsDMARD tapering
Takeuchi 2019 (RA-BEYOND)125 CDAI ≤10 12 Continued BARI 4 mg±csDMARD 281 93% <0.001
BARI Step-down 2 mg±csDMARD 278 83%

Δ, change from baseline; ACR, American College of Rheumatology; ADA, adalimumab; BARI, baricitinib; bDMARD, biological disease-modifying antirheumatic drug; CDAI, Clinical Disease Activity Index; CRP, C-reactive protein; csDMARDs, conventional synthetic disease-modifying antirheumatic drugs; CZP, certolizumab pegol; DAS28, Disease Activity Score of 28 joints; ESR, erythrocyte sedimentation rate; ETN, etanercept; EULAR, European League against Rheumatism; GC, glucocorticoid; INF, infliximab; LEF, leflunomide; mTSS, modified total Sharp Score; MTX, methotrexate; MTX, methotrexate; PLC, placebo; SJC, swollen joint count; TCZ, tocilizumab; TNFi, tumour necrosis factor inhibitor; tsDMARD, targeted synthetic DMARD.