gms | German Medical Science

Deutscher Rheumatologiekongress 2020, 48. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 34. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh)

09.09. - 12.09.2020, virtuell

Perception of the value of drugs on different manifestations of psoriatic arthritis based on a multi-stage expert opinion survey

Meeting Abstract

  • Timm Oberwahrenbrock - Fraunhofer IME, Translational Medicine & Pharmacology TMP, Frankfurt am Main; Fraunhofer Cluster of Excellence Immune-mediated Diseases CIMD, Frankfurt am Main
  • Hannah Tian - Fraunhofer IME, Translational Medicine & Pharmacology TMP, Frankfurt am Main; Fraunhofer Cluster of Excellence Immune-mediated Diseases CIMD, Frankfurt am Main
  • Diamant Thaci - Exzellenzzentrum Entzündungsmedizin UKSH Lübeck, Lübeck
  • Klaus Krüger - Rheumapraxis München, München
  • Jürgen Wollenhaupt - Rheumatologikum Hamburg, Hamburg
  • Michaela Köhm - Fraunhofer IME, Translational Medicine & Pharmacology TMP, Frankfurt am Main; Fraunhofer Cluster of Excellence Immune-mediated Diseases CIMD, Frankfurt am Main; Goethe-University Frankfurt, Rheumatology Department, Frankfurt am Main
  • Frank Behrens - Fraunhofer IME, Translational Medicine & Pharmacology TMP, Frankfurt am Main; Fraunhofer Cluster of Excellence Immune-mediated Diseases CIMD, Frankfurt am Main; Goethe-University Frankfurt, Rheumatology Department, Frankfurt am Main

Deutsche Gesellschaft für Rheumatologie. Deutsche Gesellschaft für Orthopädische Rheumatologie. Deutscher Rheumatologiekongress 2020, 48. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 34. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh). sine loco [digital], 09.-12.09.2020. Düsseldorf: German Medical Science GMS Publishing House; 2020. DocVS.10

doi: 10.3205/20dgrh195, urn:nbn:de:0183-20dgrh1957

Published: September 9, 2020

© 2020 Oberwahrenbrock et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Introduction: Patients with psoriatic arthritis (PsA) present with heterogeneous clinical phenotypes, which includes different clinical manifestations such as peripheral arthritis, axial disease, dactylitis, enthesitis, and skin and nail psoriasis. Many drugs for treatment of PsA are available for individualised treatment strategies but robust evidence is available for peripheral arthritis only as primary endpoint of RCTs.

Methods: In a face-to-face meeting, 8 German physicians (dermatology, rheumatology), specialised in PsA research/patient care, proposed initial scores for the effect size of current PsA drugs on different PsA manifestations based on knowledge of study data and personal experience in use of the drugs. The ability to achieve a consensus of the proposed efficacy scores was explored by applying an online survey among a cohort of PsA experienced physicians. Finally, a second online survey evaluated how a larger group of physicians personally estimate the drug effect sizes on different PsA manifestations.

Results: Table 1 [Tab. 1] summarises the efficacy scores proposed by the initial expert group. In the first online survey 25 treating physicians were invited to participate, 14 (56%) of whom completed the survey. An agreement rate of over 65% of the participants was archived for 49 (68%) of the 72 proposed efficacy scores (Table 1 [Tab. 1]). The consensus was especially high for the group of bDMARDs, except for etanercept and abatacept. However, the second survey (16 (39%) participants out of 41 invited physicians) revealed that the experience with the treatment using abatacept was low (4 / 16 (25%)) or non-existing (3 /16 (18.8%)) and several manifestations could not be estimated (Figure 1 [Fig. 1]). Distribution of answers were broad for etanercept in general and for particular drug-manifestation combinations (e.g. effect of ustekinumab on axial disease).

Conclusion: Many treatments are available to be used in PsA. The usage of treatment classes seems to depend on experience level and mode of action. Strategies are needed to guide physicians with lower level of experience in the use of specific drugs to achieve an optimised patient care level using personalized treatment strategies.

Disclosures: Timm Oberwahrenbrock Grant/research support from: BMS, Hannah Tian: None declared, Diamant Thaçi Grant/research support from: Janssen Research & Development, LLC, Klaus Krueger Consultant of: Celgene, Jürgen Wollenhaupt Consultant of: Celgene, Michaela Köhm Grant/research support from: Pfizer, Janssen, BMS, LEO, Consultant of: BMS, Pfizer, Speakers bureau: Pfizer, BMS, Janssen, Novartis, Frank Behrens Grant/research support from: Pfizer, Janssen, Chugai, Celgene, Lilly and Roche, Consultant of: Pfizer, AbbVie, Sanofi, Lilly, Novartis, Genzyme, Boehringer, Janssen, MSD, Celgene, Roche and Chugai