gms | German Medical Science

45. Kongress der Deutschen Gesellschaft für Rheumatologie, 31. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie, 27. Jahrestagung der Gesellschaft für Kinder- und Jugendrheumatologie

06.09. - 09.09.2017, Stuttgart

Efficacy and safety of baricitinib versus placebo and adalimumab in patients with moderately-to-severely active rheumatoid arthritis and inadequate response to methotrexate (MTX-IR): summary results from the 52-week phase 3 RA-BEAM study

Meeting Abstract

  • Peter Taylor - Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre,, Oxford, Großbritannien
  • Marek Krogulec - Rheumatology Clinic, MAK- MED, Nadarzyn, Poland
  • Anna Dudek - Centrum Medyczne AMED, Warsaw, Poland
  • Jean Dudler - HFR-Fribourg Hopital Cantonal, Service de Rhumatologie, Fribourg, Schweiz
  • E Drescher - Veszprém Csolnoky Ferenc County Hospital, Vészprem, Hungary
  • R Cseuz - Revita Clinic, Budapest, Hungary
  • Rasa Kausiene - VSI Respublikine Siauliu Ligonine, Siauliai, Lithuania
  • Daina Andersone - Pauls Stradins Clinical University Hospital, Riga, Latvia
  • Dalia Unikiene - Dr. Kildos Klinika, Kaunas, Lithuania
  • Juan Sanchez Burson - Division of Rheumatology, Hospital de Valme, Sevilla, Spain
  • Ricardo Blanco Alonso - Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Cantabria, Spain
  • Zdeněk Dvořák - Arthromed, s.r.o, Pardubice, Czech Republic
  • Andrei Petru Ghizdavescu - Eli Lilly Romania S.R.L., Bucharest, Romania
  • Ildiko Irto - Lilly Hungária Kft., Budapest, Hungary
  • Esbjörn Larsson - Eli Lilly Sweden AB, Solna, Sweden
  • Natalia Bello - Eli Lilly and Company (Spain), Alcobendas, Spain
  • Jane Barry - Lilly UK, Eli Lilly and Company Ltd, Basingstoke, UK
  • Frederick Durand - Lilly France, Neuilly-sur-Seine, France
  • Thorsten Holzkämper - Lilly Deutschland GmbH, Bad Homburg
  • Susan Otawa - Eli Lilly Canada, Toronto, Canada
  • Stephanie de Bono - Eli Lilly and Company, Indianapolis, USA
  • Edward Keystone - The Rebecca MacDonald Centre For Arthritis, Mount Sinai Hospital, Toronto, Canada
  • Andrea Rubbert-Roth - Universitätsklinikum Köln, Klinik I für Innere Medizin, Köln
  • Bernard Combe - CHRU Montpellier, Montpellier, France
  • Inmaculada de la Torre - Eli Lilly Spain, Alcobendas, Spain

Deutsche Gesellschaft für Rheumatologie. Deutsche Gesellschaft für Orthopädische Rheumatologie. Gesellschaft für Kinder- und Jugendrheumatologie. 45. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 31. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), 27. Jahrestagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR). Stuttgart, 06.-09.09.2017. Düsseldorf: German Medical Science GMS Publishing House; 2017. DocRA.03

doi: 10.3205/17dgrh156, urn:nbn:de:0183-17dgrh1566

Published: September 4, 2017

© 2017 Taylor 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

Background: Baricitinib, an oral JAK1/JAK2 inhibitor, has shown promising results in patients with active rheumatoid arthritis (RA). We present efficacy and safety results from the phase 3 RA-BEAM study in patients with active RA and inadequate response (IR) to methotrexate (MTX).

Methods: Patients with moderate-to-severe RA and MTX-IR were randomised 3:3:2 to placebo, baricitinib 4mg QD or adalimumab 40 mg biweekly. All patients continued stable background MTX therapy. Non-responders were rescued from week 16. At week 24, patients receiving placebo switched to baricitinib 4mg QD. The study compared baricitinib, placebo and adalimumab using multiple endpoints, including non-inferiority and superiority testing; primary endpoint was baricitinib versus placebo ACR20 response at week 12.

Results: Of 1305 randomised patients, 83%, 88% and 87% completed week 52 in the placebo, baricitinib and adalimumab group; rescue rates were 27%, 9% and 15%. ACR20 response at week 12 was higher for baricitinib versus placebo (p≤.001). At weeks 12 and 24, significant improvements were seen for baricitinib versus placebo in ACR20/50/70 and DAS28, CDAI and SDAI low disease activity and remission rates. Baricitinib was statistically superior to adalimumab in ACR20 responses and in DAS28-CRP at weeks 12; statistically higher ACR20 responses for baricitinib vs adalimumab were also seen at weeks 24 and 52. Change in mTSS at weeks 24 and 52 was significantly lower for baricitinib versus placebo.

At week 24, more baricitinib patients had improved physical function, and reduced fatigue and pain versus placebo and adalimumab. During weeks 0–24, more treatment-emergent AEs occurred with baricitinib and adalimumab versus placebo (71%, 67%, 60%); serious AE rates were 5%, 2% and 4%, respectively. By week 52, treatment-emergent AE rates for baricitinib versus adalimumab were 79% versus 77% and serious AE rates were 8% versus 4%; serious infection rates were similar across groups; three major cardiovascular events (2 baricitinib, 1 adalimumab), three deaths (2 baricitinib, 1 adalimumab), one tuberculosis case (adalimumab), and five malignancies (2 baricitinib, 3 placebo) were reported.

Conclusion: In patients with moderate-to-severe RA and MTX-IR receiving background MTX, addition of baricitinib was associated with significant clinical improvements versus placebo and adalimumab, with an acceptable safety profile.