The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis

<p><strong>Objective:</strong> Post hoc analysis of pooled data from 9 randomised controlled trials to assess the effect of tofacitinib (oral Janus kinase inhibitor for treatment of rheumatoid arthritis [RA] and psoriatic arthritis [PsA]) on residual pain in patients with RA or PsA...

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Main Authors: Dougados, M, Taylor, P, Bingham III, CO, Fallon, L, Brault, Y, Roychoudhury, S, Wang, L, Kessouri, M
Format: Journal article
Language:English
Published: BMJ Publishing Group 2022
_version_ 1797107858798542848
author Dougados, M
Taylor, P
Bingham III, CO
Fallon, L
Brault, Y
Roychoudhury, S
Wang, L
Kessouri, M
author_facet Dougados, M
Taylor, P
Bingham III, CO
Fallon, L
Brault, Y
Roychoudhury, S
Wang, L
Kessouri, M
author_sort Dougados, M
collection OXFORD
description <p><strong>Objective:</strong> Post hoc analysis of pooled data from 9 randomised controlled trials to assess the effect of tofacitinib (oral Janus kinase inhibitor for treatment of rheumatoid arthritis [RA] and psoriatic arthritis [PsA]) on residual pain in patients with RA or PsA with abrogated inflammation.</p> <p><strong>Methods:</strong> Patients who received ≥1 dose of tofacitinib 5 mg twice daily (BID), adalimumab or placebo with/without background conventional synthetic disease-modifying antirheumatic drugs and had abrogated inflammation (swollen joint count [SJC]=0 and C reactive protein [CRP]<6 mg/L) after 3 months’ therapy were included. Assessments included Patient’s Assessment of Arthritis Pain at Month 3 (Visual Analogue Scale [VAS] 0–100 mm). Scores were summarised descriptively; treatment comparisons assessed by Bayesian network meta analyses (BNMA).</p> <p><strong>Results:</strong> From the total RA/PsA population, 14.9% (382/2568), 17.1% (118/691) and 5.5% (50/909) of patients receiving tofacitinib, adalimumab and placebo, respectively, had abrogated inflammation after 3 months’ therapy. RA/PsA patients with abrogated inflammation receiving tofacitinib/adalimumab had higher baseline CRP versus placebo; RA patients receiving tofacitinib/adalimumab had lower SJC and longer disease duration versus placebo. Median residual pain (VAS) at Month 3 was 17.0, 19.0 and 33.5 in RA patients treated with tofacitinib, adalimumab or placebo, and 24.0, 21.0 and 27.0 in PsA patients, respectively. Residual pain reductions with tofacitinib/adalimumab versus placebo were less prominent in PsA versus RA patients, with no significant differences between tofacitinib/adalimumab, per BNMA.</p> <p><strong>Conclusion:</strong> Patients with RA/PsA with abrogated inflammation receiving tofacitinib/adalimumab had greater residual pain reduction versus placebo at Month 3. Results were similar between tofacitinib/adalimumab.</p>
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spelling oxford-uuid:97e1a651-d697-4668-bc2b-6c6e728d75902022-10-03T09:15:38ZThe effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:97e1a651-d697-4668-bc2b-6c6e728d7590EnglishSymplectic ElementsBMJ Publishing Group2022Dougados, MTaylor, PBingham III, COFallon, LBrault, YRoychoudhury, SWang, LKessouri, M<p><strong>Objective:</strong> Post hoc analysis of pooled data from 9 randomised controlled trials to assess the effect of tofacitinib (oral Janus kinase inhibitor for treatment of rheumatoid arthritis [RA] and psoriatic arthritis [PsA]) on residual pain in patients with RA or PsA with abrogated inflammation.</p> <p><strong>Methods:</strong> Patients who received ≥1 dose of tofacitinib 5 mg twice daily (BID), adalimumab or placebo with/without background conventional synthetic disease-modifying antirheumatic drugs and had abrogated inflammation (swollen joint count [SJC]=0 and C reactive protein [CRP]<6 mg/L) after 3 months’ therapy were included. Assessments included Patient’s Assessment of Arthritis Pain at Month 3 (Visual Analogue Scale [VAS] 0–100 mm). Scores were summarised descriptively; treatment comparisons assessed by Bayesian network meta analyses (BNMA).</p> <p><strong>Results:</strong> From the total RA/PsA population, 14.9% (382/2568), 17.1% (118/691) and 5.5% (50/909) of patients receiving tofacitinib, adalimumab and placebo, respectively, had abrogated inflammation after 3 months’ therapy. RA/PsA patients with abrogated inflammation receiving tofacitinib/adalimumab had higher baseline CRP versus placebo; RA patients receiving tofacitinib/adalimumab had lower SJC and longer disease duration versus placebo. Median residual pain (VAS) at Month 3 was 17.0, 19.0 and 33.5 in RA patients treated with tofacitinib, adalimumab or placebo, and 24.0, 21.0 and 27.0 in PsA patients, respectively. Residual pain reductions with tofacitinib/adalimumab versus placebo were less prominent in PsA versus RA patients, with no significant differences between tofacitinib/adalimumab, per BNMA.</p> <p><strong>Conclusion:</strong> Patients with RA/PsA with abrogated inflammation receiving tofacitinib/adalimumab had greater residual pain reduction versus placebo at Month 3. Results were similar between tofacitinib/adalimumab.</p>
spellingShingle Dougados, M
Taylor, P
Bingham III, CO
Fallon, L
Brault, Y
Roychoudhury, S
Wang, L
Kessouri, M
The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title_full The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title_fullStr The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title_full_unstemmed The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title_short The effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
title_sort effect of tofacitinib on residual pain in patients with rheumatoid arthritis and psoriatic arthritis
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