Evidence map›Paper›PMID 41525031›Full record

ArticleRheumatology and therapy2026

Rationale, Design and Methods of the Filgotinib Initial Response Study in Rheumatoid Arthritis (FIRST-RA).

Georg Pongratz, Rieke Alten, Torsten Witte, Christine Pausch, Robert Reinhold, David Pittrow, Gerd R Burmester

Abstract read
In one paragraph

Article in Rheumatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

7 authors.

Georg PongratzAbteilung für Rheumatologie und Klinische Immunologie, Krankenhaus Barmherzige Brüder, Regensburg und Fakultät für Medizin, Universität Regensburg, Regensburg, Germany.ORCID http://orcid.org/0000-0002-2185-8458
Rieke AltenSchlosspark Klinik, Akademisches Lehrkrankenhaus der Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-3395-4412
Torsten WitteKlinik für Rheumatologie und Immunologie, Medizinische Hochschule Hannover, Hannover, Germany.ORCID http://orcid.org/0000-0003-4531-0267
Christine PauschInnovationszentrum Real-World Evidence, GWT-TUD GmbH, Dresden, Germany.ORCID http://orcid.org/0000-0002-1866-9015
Robert ReinholdMedizinische Abteilung, Alfasigma GmbH, München, Germany.ORCID http://orcid.org/0009-0006-4202-3800
David PittrowInnovationszentrum Real-World Evidence, GWT-TUD GmbH, Dresden, Germany. david.pittrow@tu-dresden.de.ORCID http://orcid.org/0000-0003-1136-2616
Gerd R BurmesterMedizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0001-7518-1131

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFilgotinib is an oral Janus kinase 1 (JAK1) preferential inhibitor approved for adult patients with moderate-to-severe active rheumatoid arthritis (RA) who have responded inadequately to, or who are intolerant of, one or more disease-modifying antirheumatic drugs (DMARDs). While randomised trials have demonstrated its efficacy and tolerability, real-world data on very early treatment effects-particularly on pain relief, fatigue and function-remain scarce. The FIRST-RA study was initiated to address this evidence gap under routine care conditions.

methodsFIRST-RA is a prospective, multicentre, non-interventional cohort study in Germany and Austria. Approximately 300 adult patients with RA newly starting filgotinib are enrolled and followed for 24 weeks. Patients are stratified into three groups based on prior use of advanced therapies (AT; biologic [b]DMARDs or targeted synthetic [ts]DMARDs): AT-naïve, one prior AT and ≥ 2 prior ATs. Clinical assessments are conducted at baseline and weeks 4, 12 and 24. Patient-reported outcomes (PROs), including the Rheumatoid Arthritis Impact of Disease (RAID) questionnaire, are captured electronically or on paper- daily during week 1 and at regular intervals thereafter. PLANNED OUTCOMES: The primary endpoint is the change in RAID pain score from baseline to week 4 (or earlier). Secondary endpoints include fatigue, disease activity, morning stiffness, treatment satisfaction and tolerability. Additional analyses will investigate very early symptom changes, drug utilisation patterns and treatment persistence, as well as effectiveness within AT exposure subgroups (AT-naïve and AT-experienced), summarised descriptively without formal subgroup testing. An exploratory, descriptive analysis will examine how the 2023 label update for JAK inhibitors may have influenced patient characteristics, prescribing patterns and safety outcomes, using the earlier-enrolled FILOSOPHY real-world cohort as an external reference. FIRST-RA is the first real-world study to capture very early symptomatic responses to filgotinib. By integrating PRO data with clinical outcomes, the study aims to support personalised RA management and clarify the use of filgotinib in today's clinical practice. STUDY REGISTRATION: German Clinical Trials Register, DRKS0003613.

Indexed as

FilgotinibJAK inhibitorsPainPatient-reported outcomesRAID scoreReal-world evidence

Identifiers

PMID41525031
PMCPMC12996454

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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.