Evidence map›Paper›PMID 39707042›Full record

ArticleClinical rheumatology2025

Effectiveness of tofacitinib versus tumor necrosis factor inhibitors and in those receiving tofacitinib as different lines of therapy in patients with rheumatoid arthritis: results from the United States CorEvitas Rheumatoid Arthritis Registry.

Leslie R Harrold, Clifton O Bingham, Janet E Pope, Jacqueline O'Brien, Page C Moore, Carla Roberts-Toler, Miao Yu, Lindsay L Sweet, Ahmed Shelbaya, Karim R Masri

Registry-linked trialAbstract readComparative Study
In one paragraph

Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01402661 (CorEvitas Rheumatoid Arthritis), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT01402661 enrolling by invitationnot on this map

CorEvitas Rheumatoid Arthritis (RA) Drug Safety & Effectiveness Registry

TypeobservationalSponsorCorEvitasRan2002 to 2100Enrolled91,758ConditionsRheumatoid Arthritis
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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.

Leslie R HarroldCorEvitas, LLC, Waltham, MA, USA.ORCID http://orcid.org/0000-0002-0170-2747
Clifton O BinghamDivision of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Janet E PopeMedicine, Division Rheumatology, Western University, London, ON, Canada.ORCID http://orcid.org/0000-0003-1479-5302
Jacqueline O'BrienCorEvitas, LLC, Waltham, MA, USA.
Page C MooreCorEvitas, LLC, Waltham, MA, USA.
Carla Roberts-TolerCorEvitas, LLC, Waltham, MA, USA.
Miao YuCorEvitas, LLC, Waltham, MA, USA.
Lindsay L SweetPfizer Inc, Collegeville, PA, USA.
Ahmed ShelbayaPfizer Inc, 66 Hudson Boulevard, New York, NY, 10001, USA. Ahmed.Shelbaya@pfizer.com.ORCID http://orcid.org/0000-0003-1028-5866
Karim R MasriPfizer Inc, Collegeville, PA, USA.ORCID http://orcid.org/0000-0002-2178-9747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare effectiveness of tofacitinib versus tumor necrosis factor inhibitors (TNFi), and across tofacitinib lines of therapy, in patients with rheumatoid arthritis (RA), using US CorEvitas RA Registry data.

methodsAnalysis included patients with RA initiating tofacitinib or TNFi with a 12-month follow-up visit between November 2012-February 2021. Primary (Clinical Disease Activity Index-defined low disease activity [CDAI-LDA: CDAI ≤ 10]) and secondary (clinical/disease activity/patient-reported) effectiveness outcomes were assessed at month 12. Outcomes were stratified by treatment regimen (overall tofacitinib vs overall TNFi/tofacitinib monotherapy vs tofacitinib combination therapy/TNFi monotherapy vs TNFi combination therapy/tofacitinib monotherapy vs TNFi combination therapy/tofacitinib combination therapy vs TNFi combination therapy), or tofacitinib line of therapy (2nd/3rd/ ≥ 4th line).

results3,481 eligible patients initiated tofacitinib (n = 805) or TNFi (n = 2,676). Improvements in effectiveness at month 12 were generally similar across treatment regimens; 25.1% and 30.1% of overall tofacitinib and TNFi initiators achieved CDAI-LDA, respectively (odds ratio 1.29 [95% confidence interval (CI) 0.94, 1.76]). Odds ratios (95% CIs) for achieving CDAI-LDA at 12 months were 0.70 (0.36, 1.37) for 3rd- versus 2nd-line, and 1.09 (0.63, 1.88) for 3rd- versus ≥ 4th-line tofacitinib initiators. At month 12, mean change from baseline in CDAI was greater among 3rd- versus ≥ 4th-line tofacitinib initiators, and mean Health Assessment Questionnaire and patient-reported pain were greater in 3rd- versus 2nd-line and ≥ 4th- versus 3rd-line tofacitinib initiators.

conclusionsGenerally, there were no differences in effectiveness between tofacitinib versus TNFi regimens. Few differences were observed between tofacitinib lines of therapy; sample sizes were small for 2nd/3rd-line initiators. STUDY REGISTRATION: NCT01402661 (ClinicalTrials.gov; July 25, 2011). Key Points • Using data from the US CorEvitas rheumatoid arthritis (RA) Registry, this study compared the effectiveness of tofacitinib versus tumor necrosis factor inhibitors (TNFi) and across tofacitinib lines of therapy. • Effectiveness of tofacitinib was similar to TNFi regimens up to month 12, while differences in some effectiveness outcomes at month 12 were observed with tofacitinib across different lines of therapy. • The findings of this study may inform future treatment decision-making in patients with RA.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolesTumor Necrosis Factor InhibitorsAdultAgedDrug Therapy, CombinationFemaleHumansMaleMiddle AgedRegistriesTreatment OutcomeAntirheumatic AgentsPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolestofacitinibTumor Necrosis Factor InhibitorsComparative effectivenessDisease-modifying antirheumatic drugs (DMARDs)RegistryRheumatoid arthritis

Identifiers

PMID39707042
PMCPMC11775051

What OpenQuestion holds

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Registered trials

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.