Evidence map›Paper›PMID 38346712›Full record

Observational studyRheumatology (Oxford, England)2025

Disease activity-guided dose optimization including discontinuation of TNF inhibitors in rheumatoid arthritis is effective for up to 10 years: an observational follow-up of the DRESS study.

Céleste J T van der Togt, Nathan den Broeder, Marleen S Boonstra, Aatke van der Maas, Alfons A den Broeder, Noortje van Herwaarden

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
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

6 authors at 2 institutions in 1 country.

Céleste J T van der TogtDepartment of Rheumatology, Radboud Institute for Health Sciences, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0003-2207-9138
Nathan den BroederDepartment of Rheumatology, Radboud Institute for Health Sciences, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0001-7126-2209
Marleen S BoonstraDepartment of Rheumatology, Sint Maartenskliniek, Ubbergen, The Netherlands.
Aatke van der MaasDepartment of Rheumatology, Sint Maartenskliniek, Ubbergen, The Netherlands.
Alfons A den BroederDepartment of Rheumatology, Sint Maartenskliniek, Ubbergen, The Netherlands.
Noortje van HerwaardenDepartment of Rheumatology, Sint Maartenskliniek, Ubbergen, The Netherlands.
Radboud University Nijmegen · NLSint Maartenskliniek · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of this study was to investigate the safety and effectiveness of disease activity-guided dose optimization of TNF inhibitors in RA over 10 years.

methodsThe study involved an observational long-term extension of a randomized study of participants who completed the 3-year extension of the DRESS-study. After the randomized phase (months 0-18), disease activity-guided dose optimization was allowed for all. The main outcomes were mean time-weighted DAS28-CRP; biologic and targeted synthetic DMARD (b/tsDMARD) use per year, as proportion of daily defined dose; proportion of patients reaching discontinuation; durability and effectiveness of subsequent dose reduction attempts; and radiographic progression between years 3 and 10 using the Sharp-van der Heijde score.

resultsA total of 170 patients were included, of whom 127 completed the 10-year follow-up. The mean disease activity remained low (DAS28-CRP 2.13, 95% CI 2.10-2.16), while the b/tsDMARD dose reduced from 97% at baseline (95% CI 96-99%, n = 170) to 56% at year 10 (95% CI 49-63%, n = 127). Of 161 participants with an optimization attempt, 119 (74%) reached discontinuation with a median duration of 7 months (interquartile range 3-33 months), and 25 participants never had to restart their b/tsDMARD (21%, 95% CI 14-29%). The mean dose reduction after dose optimization was 48% (n = 159) for the first optimization attempt, and 33% for a subsequent attempt (n = 86). Of the 86 participants, 41 (48%) had radiographic progression exceeding the smallest detectable change (5.7 units), and progression was associated with disease activity, not b/tsDMARD use.

conclusionLong-term disease activity-guided dose optimization of TNF inhibitors in RA, including discontinuation and multiple tapering attempts, remains safe and effective.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidTumor Necrosis Factor InhibitorsAdultAgedDisease ProgressionDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansMaleMiddle AgedRandomized Controlled Trials as TopicSeverity of Illness IndexTreatment OutcomeAntirheumatic AgentsTumor Necrosis Factor Inhibitorsadalimumabbiologicsdose reductionetanerceptrheumatoid arthritistaperingTNF inhibitors

Identifiers

PMID38346712
PMCPMC11781578
OpenAlexW4391771775

What OpenQuestion holds

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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.