Evidence map›Paper›PMID 42334951›Full record

Observational studyRheumatology (Oxford, England)2026

Persistence and effectiveness of upadacitinib and TNFi for rheumatoid arthritis using pooled data from Canadian and Swiss registries.

Denis Choquette, Axel Finckh, Andrea Rubbert-Roth, Louis Coupal, Xiuying Li, Sibel Zehra Aydin, Helene Jonasch, Roger Gaertner, Dalinda Liazoghli, Mohammad Movahedi

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Denis ChoquetteDepartment of Rheumatology, CHUM, University of Montréal, Montréal, QC, Canada.ORCID 0000-0001-6585-7695
Axel FinckhDivision of Rheumatology, Department of Medicine, Geneva University Hospital, Geneva, Switzerland.ORCID 0000-0002-1210-4347
Andrea Rubbert-RothDepartment of Rheumatology and Immunology, Cantonal Hospital St Gallen, St Gallen, Switzerland.ORCID 0000-0002-9016-2833
Louis CoupalRHUMADATA, Institut de Recherche en Rhumatologie de Montréal, Montréal, QC, Canada.ORCID 0000-0003-0828-9665
Xiuying LiToronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.ORCID 0000-0001-6858-5947
Sibel Zehra AydinDivision of Rheumatology, University of Ottawa, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID 0000-0001-8792-4449
Helene JonaschAbbVie AG, Cham, Zug, Switzerland.ORCID 0009-0002-2526-1410
Roger GaertnerAbbVie Corporation, Saint-Laurent, QC, Canada.ORCID 0009-0006-9956-3197
Dalinda LiazoghliAbbVie Corporation, Saint-Laurent, QC, Canada.ORCID 0009-0000-0319-6131
Mohammad MovahediToronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.ORCID 0000-0001-6154-0121

Funding

AbbVieAbbVie CorpSCQM
6 · The paper itself

Abstract

objectivesThe ROSA study evaluated real-world persistence and effectiveness of upadacitinib and tumour necrosis factor inhibitors (TNFi) in patients with rheumatoid arthritis (RA), using data from two Canadian registries, RHUMADATA and Ontario Best Practices Research Initiative (OBRI), and the Swiss Clinical Quality Management in Rheumatic Diseases (SCQM) registry.

methodsThis observational study analysed data from 990 patients with RA who initiated upadacitinib or TNFi between 1 January 2020 and 30 June 2023. Multiple imputation was used for baseline covariates with missing data and results were adjusted for propensity scores derived from pre-specified variables (age, disease duration, prior treatments, comorbidities, etc.). Persistence was assessed using Kaplan-Meier and Cox proportional hazard regression models. Effectiveness was evaluated using observed (non-imputed) disease activity indices over 6 and 12 months.

resultsOverall, 174, 216 and 600 patients were included from the RHUMADATA, OBRI, SCQM registries, respectively. Patients using upadacitinib had a lower risk of discontinuing treatment than patients using TNFi [hazard-ratio (HR) (95% CI): 0.602 (0.469, 0.773)] and this was unaffected by previous exposure to advanced treatment. Concomitant use of any csDMARD HR (95% CI); [upadacitinib: 0.225 (0.107, 0.471); TNFi: 0.516 (0.303, 0.881)], and methotrexate [upadacitinib: 0.604 (0.390, 0.934); TNFi: 0.694 (0.522, 0.925)] were associated with improved persistence for both groups. A similar proportion of patients receiving upadacitinib or TNFi achieved Clinical Disease Activity Index low disease activity or remission at 6 months (70.8% vs 61.0%; P = 0.1541) and 12 months (70.5% vs 75.2%; P = 0.4494).

conclusionCanadian and Swiss patients with RA had longer persistence with upadacitinib than TNFi, independent of previous advanced treatments.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidHeterocyclic Compounds, 3-RingTumor Necrosis Factor-alphaAgedCanadaFemaleHumansMaleMiddle AgedRegistriesSwitzerlandTreatment OutcomeAntirheumatic AgentsHeterocyclic Compounds, 3-RingTumor Necrosis Factor-alphaupadacitinibeffectivenesspersistenceregistryrheumatoid arthritistumour necrosis factor inhibitorupadacitinib

Identifiers

PMID42334951
PMCPMC13313160

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.