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Abstract Number: 0335

Interleukin-17 Blockade Leads to Shifts from Stage-based Towards Response-based Disease Clusters- Comparative Data from Very Early and Established Psoriatic Arthritis

Eleni Kampylafka1, Koray Tascilar2, Veronika Lerchen3, Chistina Linz3, Maria Sokolova3, Ana Zekovic3, Arnd Kleyer2, David Simon2, Juergen Rech2, Michael Sticherling1, Georg Schett4 and Axel Hueber3, 1Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nuremberg and Universitätsklinikum Erlangen, Erlangen, Germany, 2Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nuremberg and Universitätsklinikum Erlangen, Erlangen, Bayern, Germany, 3Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander- University Erlangen-Nuremberg and University Hospital Erlangen, Erlangen, Germany, 4Friedrich-Alexander-Universität Erlangen- Nuremberg, Erlangen, Germany

Meeting: ACR Convergence 2020

Keywords: Psoriatic arthritis

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Session Information

Date: Friday, November 6, 2020

Title: Spondyloarthritis Including Psoriatic Arthritis – Diagnosis, Manifestations, & Outcomes Poster I: Psoriatic Arthritis

Session Type: Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Limited information exists about the very early forms of psoriatic arthritis (PsA). In particular, differences and responsiveness of patient-reported outcomes (PROs) in very early disease as compared to established PsA have not been investigated to date.

Methods: Cross-sectional and prospective longitudinal evaluation of PROs related to pain (VAS pain score), physical function (HAQ-DI, SF-36 physical), mental function (SF-36 mental), impact of psoriatic skin (DLQI), joint (PsAID) and global disease (VAS global) in two small prospective observational studies on secukinumab 300 mg therapy over 6 months in 20 very early disease patients (1) and 20 established PsA patients (2). Adjusted changes from baseline were estimated using linear mixed models. We performed a cluster analysis of centered and scaled PROs at baseline and 24-weeks of follow-up using Euclidean distances.

Results: While responses in pain and physical activity-related PROs to secukinumab were more pronounced in established PsA than very early disease, effects on PROs related to general health perception, as well as those related to emotional and mental well-being, were modified in a similar way in very early disease and established PsA. The absolute adjusted improvement over baseline for the specific PROs for the 2 groups of patients is presented in figure 1. Cluster analysis based on global disease activity assessment and PROs showed that baseline clusters reflected very early disease and established PsA, while during interleukin-17 inhibition these clusters were abolished and new clusters based on differential responses to physically and mentally-oriented PROs formed (figure 2).

Conclusion: Inhibition of IL-17A leads to comprehensive improvement of PROs in patients with very early musculoskeletal involvement in PsA. Most importantly, treatment restructures original clusters based on the stage of psoriatic disease and leads to the formation of clusters that reflect their post-treatment state in physical and mental-orientated PROs.

References :
1. Kampylafka E et al: Resolution of synovitis and arrest of catabolic and anabolic bone changes in patients with psoriatic arthritis by IL-17A blockade with secukinumab: results from the prospective PSARTROS study. Arthritis research & therapy 2018, 20(1):153.
2. Kampylafka E et al: Disease interception with interleukin-17 inhibition in high-risk psoriasis patients with subclinical joint inflammation-data from the prospective IVEPSA study. Arthritis research & therapy 2019, 21(1):178.

Effects of secukinumab on patient-related outcomes in patients with very early disease and established psoriatic arthritis

Pre- and post-treatment patient-related outcome based cluster analysis


Disclosure: E. Kampylafka, Novartis, 8, Bristol-Myers-Squibb, 8, Janssen, 8; K. Tascilar, None; V. Lerchen, None; C. Linz, None; M. Sokolova, None; A. Zekovic, None; A. Kleyer, Lilly, 8, Novartis, 8, BMS, 8, Sanofi, 8, Gilead, 8; D. Simon, Novartis, 8, Lilly, 5, 8, Janssen, 8, AbbVie, 5; J. Rech, Abbie, Biogen, BMS, Chugai, Celgene, EliLilly, Gilead, GSK, Janssen, MSD, Novartis, Roche, Sanofi, Sobi, UCB, 5, 8; M. Sticherling, Novartis, 2, 5, 8, Abbvie, 5, 8, Celgene, 5, 8, Janssen, 5, 8, 9, Pfizer, 8, Leo, 5, 8, Lilly, 5, 8, Sanofi, 5, 8; G. Schett, None; A. Hueber, Abbvie, 5, 8, BMS, 8, Gilead, 5, GSK, 5, 8, Janssen, 5, 8, Roche/Chugai, 5, Lilly, 2, 5, 8, Novartis, 2, 5, 8.

To cite this abstract in AMA style:

Kampylafka E, Tascilar K, Lerchen V, Linz C, Sokolova M, Zekovic A, Kleyer A, Simon D, Rech J, Sticherling M, Schett G, Hueber A. Interleukin-17 Blockade Leads to Shifts from Stage-based Towards Response-based Disease Clusters- Comparative Data from Very Early and Established Psoriatic Arthritis [abstract]. Arthritis Rheumatol. 2020; 72 (suppl 10). https://acrabstracts.org/abstract/interleukin-17-blockade-leads-to-shifts-from-stage-based-towards-response-based-disease-clusters-comparative-data-from-very-early-and-established-psoriatic-arthritis/. Accessed .
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