Rheumatoid arthritis

Better After CHoosing in rheumatoid arthritis (the BACH trial): patients who have the opportunity to choose their treatment are more satisfied

RMD OpenPublished multicentre, 24-week, open-label, randomised trial

Authors' conclusion

When allowed to choose freely, 55% of patients with RA chose an oral JAKi and 45% chose a subcutaneous TNFi. Patients who chose their own treatment had higher treatment satisfaction, better drug retention and reported fewer adverse events.

Study context

Population
Patients with biologic (DMARD)-naïve active rheumatoid arthritis (RA) after failure of conventional disease-modifying antirheumatic drugs (DMARDs)patients randomised 1:1
Participants
102 patients
Comparison
Personally choosing between subcutaneous tumour necrosis factor inhibitor (TNFi) or oral Janus kinase inhibitor (JAKi) filgotinib vs being randomised 1:1 to the same treatment options

Primary result

As reported in the abstract

Treatment chosen in the patient-choice group

Chose JAKi treatment

55%

n=28

Chose subcutaneous TNFi

45%

n=23

Further findings

OutcomePATIENT-CHOICERANDOMISEDP value
Treatment satisfaction · 24 weeksSignificantly higher in the patient-choice group4633P = 0.032
Patients who switched to a different mode of action · week 12Fewer in the patient-choice group6 events15 eventsP = 0.026
Mean Disease Activity Score in 28 joints using erythrocyte sedimentation rate · week 242.242.71P = 0.083
Glucocorticoid use · week 24More glucocorticoids used in the randomised group4 events12 eventsP = 0.031
  • Mean Disease Activity Score in 28 joints using erythrocyte sedimentation rate: numerically, but not significantly, lower in the patient-choice group

Safety

OutcomePATIENT-CHOICERANDOMISEDP value
Number of adverse events per patientSignificantly higher in the randomised group1.612.02P = 0.046

Original publication

Better After CHoosing in rheumatoid arthritis (the BACH trial): patients who have the opportunity to choose their treatment are more satisfied. RMD Open. Published 27 October 2026. doi:10.1136/rmdopen-2026-007406

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