4.4 Article

Using adalimumab serum concentration to choose a subsequent biological DMARD in rheumatoid arthritis patients failing adalimumab treatment (ADDORA-switch): study protocol for a fully blinded randomised superiority test-treatment trial

期刊

TRIALS
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13063-021-05358-7

关键词

Rheumatoid arthritis; Adalimumab; Anti-TNF; Therapeutic drug monitoring; Drug concentration; Switching; Test-treatment trial; Design

资金

  1. ZonMw [8481 01 006]
  2. Sanquin Diagnostics

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This study investigates the clinical utility of therapeutic drug monitoring (TDM) in guiding treatment for patients with rheumatoid arthritis. It is the first blinded test-treatment trial using TDM in this context, with a unique design compared to previous TDM studies.
BackgroundA substantial proportion of rheumatoid arthritis (RA) patients discontinues treatment with tumour necrosis factor inhibitors (TNFi) due to inefficacy or intolerance. After the failure of treatment with a TNFi, treatment can be switched to another TNFi or a bDMARD with a different mode of action (non-TNFi). Measurement of serum drug concentrations and/or anti-drug antibodies (therapeutic drug monitoring (TDM)) may help to inform the choice for the next step. However, the clinical utility of TDM to guide switching has not been investigated in a randomised test-treatment study.MethodsADDORA-switch is a 24-week, multi-centre, triple-blinded, superiority test-treatment randomised controlled trial. A total of 84 RA patients failing adalimumab treatment (treatment failure defined as DAS28-CRP > 2.9) will be randomised in a 1:1 ratio to a switching strategy to either TNFi or non-TNFi based on adalimumab serum trough level (intervention group) or random allocation (control group). The primary outcome is the between-group difference in mean time-weighted DAS28 over 24weeks.DiscussionThe trial design differs in many aspects from previously published and ongoing TDM studies and is considered the first blinded test-treatment trial using TDM in RA. Several choices in the design of this trial are described, and overarching principles regarding test-treatment trials and clinical utility of TDM are discussed in further detail.Trial registrationDutch Trial Register NL8210. Registered on 3 December 2019 (CMO NL69841.091.19).

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