Radiographic  progression was assessed in two phase 3 randomized-controlled trials.  Methotrexate-naïve patients were randomized to upadacitinib 15 or 30 mg once  daily (QD) or methotrexate monotherapy (SELECT-EARLY, n = 945), while  methotrexate inadequate responders (IR) were randomized to upadacitinib 15 mg  QD or adalimumab 40 mg every other week or placebo added to background  methotrexate (SELECT-COMPARE, n = 1629). Mean changes from baseline in modified  Total Sharp Score (mTSS), joint space narrowing (JSN), and erosion scores (ES)  were determined. Data were analysed both by linear extrapolation for missing  data imputation and treatment switching and as-observed.
    Results:
    In patients  naïve or with limited exposure to methotrexate (SELECT-EARLY), mean changes  from baseline to week 48 in mTSS were 0.03 for upadacitinib 15 mg, 0.14 for  upadacitinib 30 mg, and 1.00 for methotrexate based on linear extrapolation (p  < 0.001 for both upadacitinib doses vs methotrexate). Among patients with an  inadequate response to methotrexate (SELECT-COMPARE), the mean change from baseline  in mTSS was significantly reduced in the upadacitinib 15 mg plus methotrexate  group vs placebo plus methotrexate (0.28 vs 1.73; p < 0.001); mean change  from baseline in the adalimumab plus methotrexate group was 0.39.
    Upadacitinib  monotherapy or in combination with background methotrexate was effective in  inhibiting the progression of structural joint damage through week 48 in  methotrexate-naïve and methotrexate-IR patients with RA.
    Reference:
    Peterfy CG, Strand V, Friedman A, et al. Inhibition of  Structural Joint Damage Progression with Upadacitinib in Rheumatoid Arthritis:  1-Year Outcomes from the SELECT Phase 3 Program [published online ahead of  print, 2021 Dec 13]. Rheumatology (Oxford). 2021;keab861.  doi:10.1093/rheumatology/keab861
 
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