gms | German Medical Science

Deutscher Rheumatologiekongress 2021, 49. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 35. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), Wissenschaftliche Herbsttagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR)

15.09. - 18.09.2021, virtuell

Treatment of interleukin 6 inhibitor in severe ankylosing spondylitis with second AA-amyloidosis

Meeting Abstract

  • Daria Rumiantceva - V.A. Nasonova Research institute of Rheumatology, Laboratory ofSspondyloarthritis and Psoriatic Arthritis, Moscow
  • Екатерина Агафонова - V.A. Nasonova Research institute of Rheumatology, Laboratory ofSspondyloarthritis and Psoriatic Arthritis, Moscow
  • Margarita Urumova - V.A. Nasonova Research institute of Rheumatology, Laboratory ofSspondyloarthritis and Psoriatic Arthritis, Moscow
  • Shandor Erdes - V.A. Nasonova Research institute of Rheumatology, Laboratory ofSspondyloarthritis and Psoriatic Arthritis, Moscow

Deutsche Gesellschaft für Rheumatologie. Deutsche Gesellschaft für Orthopädische Rheumatologie. Gesellschaft für Kinder- und Jugendrheumatologie. Deutscher Rheumatologiekongress 2021, 49. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 35. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), Wissenschaftliche Herbsttagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR). sine loco [digital], 15.-18.09.2021. Düsseldorf: German Medical Science GMS Publishing House; 2021. DocSpA.49

doi: 10.3205/21dgrh164, urn:nbn:de:0183-21dgrh1642

Veröffentlicht: 14. September 2021

© 2021 Rumiantceva et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Introduction: Inhibitors of interleukin 6 (IL6) have been found to be ineffective in ankylosing spondylitis (AS) based on the results of randomized clinical trials (RCTs) on tocilizumab (TCZ) and sarilimumab. However, there is evidence that IL6 is actively involved in the pathogenesis of the disease. In addition, the efficacy of IL6 inhibitors has been shown in patients with secondary AA-amyloidosis. Aim: to analyze the effectiveness of IL6 inhibitor - TCZ in patients with AS with high disease activity and secondary AA-amyloidosis.

Methods: The analysis included 10 patients with AS receiving TCZ therapy, of which 8 (80%) men, 2 (20%) women, and 100% HLA B27 positive. The average age of the patients was 40 ± 8.6 years, the average duration of AS was 25.6 ± 6.5 years. 9 patients had histologically confirmed secondary AA-amyloidosis: 100% had kidney amyloidosis, 6 (66.6%) patients also had gastrointestinal amyloidosis and 3 (33.4%) patients had heart amyloidosis. The average duration of TCZ treatment was 22.0 months [1.0; 36.0]. 8 (80%) patients continue to take TCZ therapy to date, and 2 (20%) - are transferred to TNF-α inhibitors.

Results: Table 1 [Tab. 1] shows the main clinical and laboratory characteristics of patients at the initiation of TCZ therapy and during the therapy. As you can see, against the background of TCZ therapy, both the level of CRP, proteinuria and the indices of AS activity (BASDAI, ASDAS CRP) significantly decreased. The number of patients with inflammatory back pain (IBP), arthritis and coxitis also decreased significantly.

Conclusion: The above data showed that the method of treating AS with IL6 inhibitors, in certain clinical situations, primarily such as ineffectiveness of TNF-α inhibitors, high CRP level and the development of secondary AA-amyloidosis, can be highly effective.

Disclosures: no.