Rheumatoid arthritis

Impact of initial therapy with upadacitinib or adalimumab on achievement of 48-week treatment goals in patients with rheumatoid arthritis: post hoc analysis of SELECT-COMPARE

Rheumatology (Oxford)Published Post hoc analysis of the SELECT-COMPARE randomised trial

Authors' conclusion

Following a modified treat-to-target strategy, rates of CDAI remission/LDA and DAS28(CRP) <2.6/≤3.2 at 48 weeks were similar, regardless of starting therapy. However, patients initially receiving upadacitinib reached treatment targets more quickly and spent more time in clinical targets over the initial 48 weeks of treatment.

Study context

Population
Patients with RA and inadequate MTX response in SELECT-COMPARE
Participants
651 vs 327
Comparison
Initial upadacitinib vs initial adalimumab after inadequate MTX response
  • Upadacitinibn = 651
  • Adalimumabn = 327reference
Primary endpoint
Achievement of treatment goals (clinical remission/low disease activity (LDA), physical function, pain, combined deep-response endpoint) and time-averaged response rates
Follow-up
48 weeks
Methodological detailsblinded switch (modified treat-to-target), analysed by initial randomized group regardless of switch
  • Blinded switch (modified treat-to-target)
  • Analysed by initial randomized group regardless of switch

Primary result

As reported in the abstract

Treatment endpoints at week 48

Median time to DAS28(CRP) <2.6/≤3.2 earlier with initial upadacitinib

6-8 weeks

Original publication

Impact of initial therapy with upadacitinib or adalimumab on achievement of 48-week treatment goals in patients with rheumatoid arthritis: post hoc analysis of SELECT-COMPARE. Rheumatology (Oxford). Published 26 August 2022. doi:10.1093/rheumatology/keac477

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