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Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension

OBJECTIVE: Evaluate open-label sarilumab monotherapy in patients with rheumatoid arthritis switching from adalimumab monotherapy in MONARCH (NCT02332590); assess long-term safety and efficacy in patients continuing sarilumab during open-label extension (OLE). METHODS: During the 48-week OLE, patient...

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Autores principales: Burmester, Gerd R, Strand, Vibeke, Rubbert-Roth, Andrea, Amital, Howard, Raskina, Tatiana, Gómez-Centeno, Antonio, Pena-Rossi, Claudia, Gervitz, Leon, Thangavelu, Karthinathan, St John, Gregory, Boklage, Susan, Genovese, Mark C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802992/
https://www.ncbi.nlm.nih.gov/pubmed/31673415
http://dx.doi.org/10.1136/rmdopen-2019-001017
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author Burmester, Gerd R
Strand, Vibeke
Rubbert-Roth, Andrea
Amital, Howard
Raskina, Tatiana
Gómez-Centeno, Antonio
Pena-Rossi, Claudia
Gervitz, Leon
Thangavelu, Karthinathan
St John, Gregory
Boklage, Susan
Genovese, Mark C
author_facet Burmester, Gerd R
Strand, Vibeke
Rubbert-Roth, Andrea
Amital, Howard
Raskina, Tatiana
Gómez-Centeno, Antonio
Pena-Rossi, Claudia
Gervitz, Leon
Thangavelu, Karthinathan
St John, Gregory
Boklage, Susan
Genovese, Mark C
author_sort Burmester, Gerd R
collection PubMed
description OBJECTIVE: Evaluate open-label sarilumab monotherapy in patients with rheumatoid arthritis switching from adalimumab monotherapy in MONARCH (NCT02332590); assess long-term safety and efficacy in patients continuing sarilumab during open-label extension (OLE). METHODS: During the 48-week OLE, patients received sarilumab 200 mg subcutaneously once every 2 weeks. Safety (March 2017 cut-off) and efficacy, including patient-reported outcomes, were evaluated. RESULTS: In the double-blind phase, patients receiving sarilumab or adalimumab monotherapy showed meaningful improvements in disease activity; sarilumab was superior to adalimumab for improving signs, symptoms and physical function. Overall, 320/369 patients completing the 24-week double-blind phase entered OLE (155 switched from adalimumab; 165 continued sarilumab). Sarilumab safety profile was consistent with previous reports. Treatment-emergent adverse events were similar between groups; no unexpected safety signals emerged in the first 10 weeks postswitch. Among switch patients, improvement in disease activity was evident at OLE week 12: 47.1%/34.8% had changes ≥1.2 in Disease Activity Score (28 joints) (DAS28)-erythrocyte sedimentation rate/DAS28-C-reactive protein. In switch patients achieving low disease activity (LDA: Clinical Disease Activity Index (CDAI) ≤10; Simplified Disease Activity Index (SDAI) ≤11) by OLE week 24, 70.7%/69.5% sustained CDAI/SDAI LDA at both OLE weeks 36 and 48. Proportions of switch patients achieving CDAI ≤2.8 and SDAI ≤3.3 by OLE week 24 increased through OLE week 48. Improvements postswitch approached continuation-group values, including scores ≥normative values. CONCLUSIONS: During this OLE, there were no unexpected safety issues in patients switching from adalimumab to sarilumab monotherapy, and disease activity improved in many patients. Patients continuing sarilumab reported safety consistent with prolonged use and had sustained benefit.
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spelling pubmed-68029922019-10-31 Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension Burmester, Gerd R Strand, Vibeke Rubbert-Roth, Andrea Amital, Howard Raskina, Tatiana Gómez-Centeno, Antonio Pena-Rossi, Claudia Gervitz, Leon Thangavelu, Karthinathan St John, Gregory Boklage, Susan Genovese, Mark C RMD Open Rheumatoid Arthritis OBJECTIVE: Evaluate open-label sarilumab monotherapy in patients with rheumatoid arthritis switching from adalimumab monotherapy in MONARCH (NCT02332590); assess long-term safety and efficacy in patients continuing sarilumab during open-label extension (OLE). METHODS: During the 48-week OLE, patients received sarilumab 200 mg subcutaneously once every 2 weeks. Safety (March 2017 cut-off) and efficacy, including patient-reported outcomes, were evaluated. RESULTS: In the double-blind phase, patients receiving sarilumab or adalimumab monotherapy showed meaningful improvements in disease activity; sarilumab was superior to adalimumab for improving signs, symptoms and physical function. Overall, 320/369 patients completing the 24-week double-blind phase entered OLE (155 switched from adalimumab; 165 continued sarilumab). Sarilumab safety profile was consistent with previous reports. Treatment-emergent adverse events were similar between groups; no unexpected safety signals emerged in the first 10 weeks postswitch. Among switch patients, improvement in disease activity was evident at OLE week 12: 47.1%/34.8% had changes ≥1.2 in Disease Activity Score (28 joints) (DAS28)-erythrocyte sedimentation rate/DAS28-C-reactive protein. In switch patients achieving low disease activity (LDA: Clinical Disease Activity Index (CDAI) ≤10; Simplified Disease Activity Index (SDAI) ≤11) by OLE week 24, 70.7%/69.5% sustained CDAI/SDAI LDA at both OLE weeks 36 and 48. Proportions of switch patients achieving CDAI ≤2.8 and SDAI ≤3.3 by OLE week 24 increased through OLE week 48. Improvements postswitch approached continuation-group values, including scores ≥normative values. CONCLUSIONS: During this OLE, there were no unexpected safety issues in patients switching from adalimumab to sarilumab monotherapy, and disease activity improved in many patients. Patients continuing sarilumab reported safety consistent with prolonged use and had sustained benefit. BMJ Publishing Group 2019-10-18 /pmc/articles/PMC6802992/ /pubmed/31673415 http://dx.doi.org/10.1136/rmdopen-2019-001017 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Rheumatoid Arthritis
Burmester, Gerd R
Strand, Vibeke
Rubbert-Roth, Andrea
Amital, Howard
Raskina, Tatiana
Gómez-Centeno, Antonio
Pena-Rossi, Claudia
Gervitz, Leon
Thangavelu, Karthinathan
St John, Gregory
Boklage, Susan
Genovese, Mark C
Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title_full Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title_fullStr Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title_full_unstemmed Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title_short Safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing MONARCH open-label extension
title_sort safety and efficacy of switching from adalimumab to sarilumab in patients with rheumatoid arthritis in the ongoing monarch open-label extension
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802992/
https://www.ncbi.nlm.nih.gov/pubmed/31673415
http://dx.doi.org/10.1136/rmdopen-2019-001017
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