Evidence map›Paper›PMID 38840219›Full record

ReviewArthritis research & therapy2024

Effectiveness of janus kinase inhibitors in relapsing giant cell arteritis in real-world clinical practice and review of the literature.

Javier Loricera, Toluwalase Tofade, Diana Prieto-Peña, Susana Romero-Yuste, Eugenio de Miguel, Anne Riveros-Frutos, Iván Ferraz-Amaro, Eztizen Labrador, Olga Maiz, Elena Becerra and 9 more

Registry-linked trialAbstract readReviewMulticenter Study
In one paragraph

Review in Arthritis research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03725202 (A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Upadacitinib in Subjects With Giant Cell Arteritis), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

NCT03725202 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Upadacitinib in Subjects With Giant Cell Arteritis: SELECT-GCA

TypeinterventionalSponsorAbbVieRan2019 to 2025Enrolled429ConditionsGiant Cell Arteritis (GCA)ArmsUpadacitinib, Corticosteroid (CS), Placebo
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. 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

19 authors.

Javier Loricera *Department of Rheumatology, IDIVAL, Immunopathology Group, Hospital Universitario Marqués de Valdecilla, Avda. Valdecilla s/n, Santander, ES- 39008, Spain.
Toluwalase Tofade *Neurology Department, Massachusetts General Hospital, Boston, MA, USA.
Diana Prieto-PeñaDepartment of Rheumatology, IDIVAL, Immunopathology Group, Hospital Universitario Marqués de Valdecilla, Avda. Valdecilla s/n, Santander, ES- 39008, Spain.
Susana Romero-YusteDepartment of Rheumatology, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain.
Eugenio de MiguelDepartment of Rheumatology, Hospital Universitario La Paz, Madrid, Spain.
Anne Riveros-FrutosDepartment of Rheumatology, Hospital Universitario Germans Trias i Pujol, Badalona, Spain.
Iván Ferraz-AmaroDepartment of Rheumatology, Complejo Hospitalario Universitario de Canarias, Santa Cruz de Tenerife, Spain.
Eztizen LabradorDepartment of Rheumatology, Hospital San Pedro, Logroño, Spain.
Olga MaizDepartment of Rheumatology, Hospital Universitario de Donosti, San Sebastián, Spain.
Elena BecerraDepartment of Rheumatology, Hospital Universitario de Elda, Alicante, Spain.
Javier NarváezDepartment of Rheumatology, Hospital de Bellvitge, Barcelona, Spain.
Eva Galíndez-AgirregoikoaDepartment of Rheumatology, Hospital Universitario de Basurto, Bilbao, Spain.
Ismael González-FernándezDepartment of Rheumatology, Complejo Asistencial Universitario de León, León, Spain.
Ana Urruticoechea-AranaDepartment of Rheumatology, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
Ángel Ramos-CalvoDepartment of Rheumatology, Complejo Hospitalario de Soria, Soria, Spain.
Fernando López-GutiérrezDepartment of Rheumatology, IDIVAL, Immunopathology Group, Hospital Universitario Marqués de Valdecilla, Avda. Valdecilla s/n, Santander, ES- 39008, Spain.
Santos Castañeda *Department of Rheumatology, Hospital Universitario La Princesa, IIS-Princesa, Madrid, Spain.
Sebastian Unizony *Vasculitis and Glomerulonephritis Center, Rheumatology, Immunology and Allergy Division, Massachusetts General Hospital, Boston, MA, 02114, USA. sunizony@mgh.harvard.edu.ORCID 0000-0002-8935-7473
Ricardo Blanco *Department of Rheumatology, IDIVAL, Immunopathology Group, Hospital Universitario Marqués de Valdecilla, Avda. Valdecilla s/n, Santander, ES- 39008, Spain. rblancovela@gmail.com.ORCID 0000-0003-2344-2285

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA substantial proportion of patients with giant cell arteritis (GCA) relapse despite standard therapy with glucocorticoids, methotrexate and tocilizumab. The Janus kinase/signal transducer and activator of transcription (JAK/STAT) signalling pathway is involved in the pathogenesis of GCA and JAK inhibitors (JAKi) could be a therapeutic alternative. We evaluated the effectiveness of JAKi in relapsing GCA patients in a real-world setting and reviewed available literature.

methodsRetrospective analysis of GCA patients treated with JAKi for relapsing disease at thirteen centers in Spain and one center in United States (01/2017-12/2022). Outcomes assessed included clinical remission, complete remission and safety. Clinical remission was defined as the absence of GCA signs and symptoms regardless of the erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) values. Complete remission was defined as the absence of GCA signs and symptoms along with normal ESR and CRP values. A systematic literature search for other JAKi-treated GCA cases was conducted.

resultsThirty-five patients (86% females, mean age 72.3) with relapsing GCA received JAKi therapy (baricitinib, n = 15; tofacitinib, n = 10; upadacitinib, n = 10). Before JAKi therapy, 22 (63%) patients had received conventional synthetic immunosuppressants (e.g., methotrexate), and 30 (86%) biologics (e.g., tocilizumab). After a median (IQR) follow-up of 11 (6-15.5) months, 20 (57%) patients achieved and maintained clinical remission, 16 (46%) patients achieved and maintained complete remission, and 15 (43%) patients discontinued the initial JAKi due to relapse (n = 11 [31%]) or serious adverse events (n = 4 [11%]). A literature search identified another 36 JAKi-treated GCA cases with clinical improvement reported for the majority of them.

conclusionsThis real-world analysis and literature review suggest that JAKi could be effective in GCA, including in patients failing established glucocorticoid-sparing therapies such as tocilizumab and methotrexate. A phase III randomized controlled trial of upadacitinib is currently ongoing (ClinicalTrials.gov ID NCT03725202).

Indexed as

Giant Cell ArteritisJanus Kinase InhibitorsAgedAged, 80 and overAzetidinesFemaleHeterocyclic Compounds, 3-RingHumansMaleMiddle AgedPiperidinesPurinesPyrazolesPyrimidinesRecurrenceRetrospective StudiesAzetidinesbaricitinibHeterocyclic Compounds, 3-RingJanus Kinase InhibitorsPiperidinesPurinesPyrazolesPyrimidinesSulfonamidestofacitinibupadacitinibBaricitinibGiant cell arteritisJanus kinase inhibitorsLarge vessel vasculitisTofacitinibUpadacitinib

Identifiers

PMID38840219
PMCPMC11151571

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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.