Drug retention, inactive disease and response rates in 1860 patients with axial spondyloarthritis initiating secukinumab treatment: routine care data from 13 registries in the EuroSpA collaboration. Issue 3 (19th September 2020)
- Record Type:
- Journal Article
- Title:
- Drug retention, inactive disease and response rates in 1860 patients with axial spondyloarthritis initiating secukinumab treatment: routine care data from 13 registries in the EuroSpA collaboration. Issue 3 (19th September 2020)
- Main Title:
- Drug retention, inactive disease and response rates in 1860 patients with axial spondyloarthritis initiating secukinumab treatment: routine care data from 13 registries in the EuroSpA collaboration
- Authors:
- Michelsen, Brigitte
Lindström, Ulf
Codreanu, Catalin
Ciurea, Adrian
Zavada, Jakub
Loft, Anne Gitte
Pombo-Suarez, Manuel
Onen, Fatos
Kvien, Tore K
Rotar, Ziga
Santos, Maria Jose
Iannone, Florenzo
Hokkanen, Anna-Mari
Gudbjornsson, Bjorn
Askling, Johan
Ionescu, Ruxandra
Nissen, Michael J
Pavelka, Karel
Sanchez-Piedra, Carlos
Akar, Servet
Sexton, Joseph
Tomsic, Matija
Santos, Helena
Sebastiani, Marco
Österlund, Jenny
Geirsson, Arni Jon
Macfarlane, Gary
van der Horst-Bruinsma, Irene
Georgiadis, Stylianos
Brahe, Cecilie Heegaard
Ørnbjerg, Lykke Midtbøll
Hetland, Merete Lund
Østergaard, Mikkel
… (more) - Abstract:
- Abstract : Objectives: To explore 6-month and 12-month secukinumab effectiveness in patients with axial spondyloarthritis (axSpA) overall, as well as across (1) number of previous biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs), (2) time since diagnosis and (3) different European registries. Methods: Real-life data from 13 European registries participating in the European Spondyloarthritis Research Collaboration Network were pooled. Kaplan-Meier with log-rank test, Cox regression, χ² and logistic regression analyses were performed to assess 6-month and 12-month secukinumab retention, inactive disease/low-disease-activity states (Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) <2/<4, Ankylosing Spondylitis Disease Activity Score (ASDAS) <1.3/<2.1) and response rates (BASDAI50, Assessment of Spondyloarthritis International Society (ASAS) 20/40, ASDAS clinically important improvement (ASDAS-CII) and ASDAS major improvement (ASDAS-MI)). Results: We included 1860 patients initiating secukinumab as part of routine care. Overall 6-month/12-month secukinumab retention rates were 82%/72%, with significant (p<0.001) differences between the registries (6-month: 70–93%, 12-month: 53–86%) and across number of previous b/tsDMARDs (b/tsDMARD-naïve: 90%/84%, 1 prior b/tsDMARD: 83%/73%, ≥2 prior b/tsDMARDs: 78%/66%). Overall 6-month/12-month BASDAI<4 were observed in 51%/51%, ASDAS<1.3 in 9%/11%, BASDAI50 in 53%/47%, ASAS40 in 28%/22%, ASDAS-CII inAbstract : Objectives: To explore 6-month and 12-month secukinumab effectiveness in patients with axial spondyloarthritis (axSpA) overall, as well as across (1) number of previous biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs), (2) time since diagnosis and (3) different European registries. Methods: Real-life data from 13 European registries participating in the European Spondyloarthritis Research Collaboration Network were pooled. Kaplan-Meier with log-rank test, Cox regression, χ² and logistic regression analyses were performed to assess 6-month and 12-month secukinumab retention, inactive disease/low-disease-activity states (Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) <2/<4, Ankylosing Spondylitis Disease Activity Score (ASDAS) <1.3/<2.1) and response rates (BASDAI50, Assessment of Spondyloarthritis International Society (ASAS) 20/40, ASDAS clinically important improvement (ASDAS-CII) and ASDAS major improvement (ASDAS-MI)). Results: We included 1860 patients initiating secukinumab as part of routine care. Overall 6-month/12-month secukinumab retention rates were 82%/72%, with significant (p<0.001) differences between the registries (6-month: 70–93%, 12-month: 53–86%) and across number of previous b/tsDMARDs (b/tsDMARD-naïve: 90%/84%, 1 prior b/tsDMARD: 83%/73%, ≥2 prior b/tsDMARDs: 78%/66%). Overall 6-month/12-month BASDAI<4 were observed in 51%/51%, ASDAS<1.3 in 9%/11%, BASDAI50 in 53%/47%, ASAS40 in 28%/22%, ASDAS-CII in 49%/46% and ASDAS-MI in 25%/26% of the patients. All rates differed significantly across number of previous b/tsDMARDs, were numerically higher for b/tsDMARD-naïve patients and varied significantly across registries. Overall, time since diagnosis was not associated with secukinumab effectiveness. Conclusions: In this study of 1860 patients from 13 European countries, we present the first comprehensive real-life data on effectiveness of secukinumab in patients with axSpA. Overall, secukinumab retention rates after 6 and 12 months of treatment were high. Secukinumab effectiveness was consistently better for bionaïve patients, independent of time since diagnosis and differed across the European countries. … (more)
- Is Part Of:
- RMD open. Volume 6:Issue 3(2020)
- Journal:
- RMD open
- Issue:
- Volume 6:Issue 3(2020)
- Issue Display:
- Volume 6, Issue 3 (2020)
- Year:
- 2020
- Volume:
- 6
- Issue:
- 3
- Issue Sort Value:
- 2020-0006-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-09-19
- Subjects:
- Spondyloarthritis -- DMARDs (biologic) -- Outcomes research
Musculoskeletal system -- Diseases -- Periodicals
Rheumatism -- Periodicals
616.7005 - Journal URLs:
- http://www.bmj.com/archive ↗
http://rmdopen.bmj.com/ ↗ - DOI:
- 10.1136/rmdopen-2020-001280 ↗
- Languages:
- English
- ISSNs:
- 2056-5933
- Deposit Type:
- Legaldeposit
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- British Library DSC - BLDSS-3PM
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