TY - JOUR
T1 - Achieving pain control in early rheumatoid arthritis with baricitinib monotherapy or in combination with methotrexate versus methotrexate monotherapy
AU - Taylor, Peter C.
AU - Alten, Rieke
AU - Álvaro Gracia, Jose Mariá
AU - Kaneko, Yuko
AU - Walls, Chad
AU - Quebe, Amanda
AU - Jia, Bochao
AU - Bello, Natalia
AU - Terres, Jorge Ross
AU - Fleischmann, Roy
N1 - Funding Information:
Competing interests PCT has received research grants and/or consultation fees from Galapagos, Gilead, Eli Lilly and Company, AbbVie, and Pfizer. Rieke Alten has received honoraria and research grants from Abbvie, BMS, Galalapagos, Gilead, Janssen, Lilly, MSD, Novartis and Pfizer. JMAG has received consulting fees from Eli Lilly and Company and Pfizer; honoraria from Abbvie, Eli Lilly and Company, Galapagos, Gilead, Pfizer, Roche and UCB; and support for attending meetings from Abbvie, MSD, Pfizer, Roche and UCB. YK has received grants or speaking fees from AbbVie, Astellas, Ayumi, Bristol–Myers Squibb, Chugai, Eisai, Eli Lilly and Company, Jansen, Kissei, Kirin, Novartis pharma, Pfizer, Sanofi, Takeda, Tanabe-Mitsubishi and UCB. CW, AQ, BJ, NB and JRT are employees and may be shareholders of Eli Lilly and Company. RF has received grants from AbbVie, Eli Lilly and Company, Gilead, and Pfizer; consulting fees from AbbVie, Eli Lilly and Company, Gilead, and Pfizer; and participated on a Data Safety Monitoring Board or Advisory Board for AbbVie, Eli Lilly and Company, Gilead and Pfizer.
Funding Information:
1Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences, University of Oxford, Oxford, UK 2Internal Medicine II, Rheumatology, SCHLOSSPARK-KLINIK, University Medicine Berlin, Berlin, Germany 3Rheumatology Department, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain 4Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan 5Eli Lilly and Company, Indianapolis, Indiana, USA 6Metroplex Clinical Research Center, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, USA Acknowledgements The authors thank the participants, caregivers, and investigators. The authors would like to acknowledge Catherine Lynch of Eli Lilly and Company for assistance with manuscript preparation and process support. PCT thanks the National Institute of Health Research for their funding of The NIHR Biomedical Research Centre in Musculoskeletal Disease at Oxford University Hospitals NHS Trust and the University of Oxford.
Funding Information:
Funding This study and manuscript were sponsored by Eli Lilly and Company under license from Incyte Corporation.
Publisher Copyright:
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2022/3/9
Y1 - 2022/3/9
N2 - Objectives This post hoc analysis assessed speed, magnitude and maintenance of pain improvement in patients with early rheumatoid arthritis (RA) receiving baricitinib, baricitinib and methotrexate (MTX), or MTX over 1 year. Cumulative pain and quality of life benefits were also assessed. Methods Randomised, double-blind, phase 3 study RA-BEGIN (NCT01711359) compared baricitinib 4 mg (N=159), baricitinib 4 mg +MTX (N=215) and MTX (N=210) in patients with RA who had no or limited prior disease-modifying antirheumatic drug treatment. Pain was assessed on a 0-100 mm Visual Analogue Scale (VAS). Proportion of patients with ≥30%, ≥50% and ≥70% pain improvement from baseline; ≤20 mm and ≤10 mm on the pain VAS; and time to achieve pain improvement thresholds were assessed over 52 weeks, as were Patient Global Assessment (PtGA) and 36-Item Short Form Health Survey Physical Component Score (SF-36 PCS) outcomes. Results Baricitinib monotherapy or combination with MTX provides greater (least square mean changes (LSM) from baseline -40 mm and -43 mm, respectively) and more rapid (median 12 and 8 weeks to ≥70% improvement, respectively) pain relief than MTX alone (LSM -31 mm, median 20 weeks to ≥70% improvement) over 52 weeks. Baricitinib, alone or combination, provides 9-10 additional weeks of limited to no pain, similar gain in achievable wellness measured through PtGA, and 5-7 additional weeks with change in SF-36 PCS ≥5 vs MTX over 1 year. Conclusions Patients treated with baricitinib reported significantly greater and more rapid pain relief, more weeks with limited to no pain, and clinically meaningful improvements in physical health than patients treated with MTX alone over 1 year.
AB - Objectives This post hoc analysis assessed speed, magnitude and maintenance of pain improvement in patients with early rheumatoid arthritis (RA) receiving baricitinib, baricitinib and methotrexate (MTX), or MTX over 1 year. Cumulative pain and quality of life benefits were also assessed. Methods Randomised, double-blind, phase 3 study RA-BEGIN (NCT01711359) compared baricitinib 4 mg (N=159), baricitinib 4 mg +MTX (N=215) and MTX (N=210) in patients with RA who had no or limited prior disease-modifying antirheumatic drug treatment. Pain was assessed on a 0-100 mm Visual Analogue Scale (VAS). Proportion of patients with ≥30%, ≥50% and ≥70% pain improvement from baseline; ≤20 mm and ≤10 mm on the pain VAS; and time to achieve pain improvement thresholds were assessed over 52 weeks, as were Patient Global Assessment (PtGA) and 36-Item Short Form Health Survey Physical Component Score (SF-36 PCS) outcomes. Results Baricitinib monotherapy or combination with MTX provides greater (least square mean changes (LSM) from baseline -40 mm and -43 mm, respectively) and more rapid (median 12 and 8 weeks to ≥70% improvement, respectively) pain relief than MTX alone (LSM -31 mm, median 20 weeks to ≥70% improvement) over 52 weeks. Baricitinib, alone or combination, provides 9-10 additional weeks of limited to no pain, similar gain in achievable wellness measured through PtGA, and 5-7 additional weeks with change in SF-36 PCS ≥5 vs MTX over 1 year. Conclusions Patients treated with baricitinib reported significantly greater and more rapid pain relief, more weeks with limited to no pain, and clinically meaningful improvements in physical health than patients treated with MTX alone over 1 year.
KW - arthritis, rheumatoid
KW - patient reported outcome measures
KW - therapeutics
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U2 - 10.1136/rmdopen-2021-001994
DO - 10.1136/rmdopen-2021-001994
M3 - Article
C2 - 35264432
AN - SCOPUS:85126076049
SN - 2056-5933
VL - 8
JO - RMD Open
JF - RMD Open
IS - 1
M1 - e001994
ER -