Evidence map›Paper›PMID 42573952›Full record

ReviewAdvances in therapy2026

Golimumab for the Treatment of Axial Spondyloarthritis: Integrating Clinical Outcomes with Real-World Patient Benefits.

Atul Deodhar, Tae-Jong Kim, Victoria Navarro-Compán, Sergio Fonseca, José Antunes, Arun Singh, Richard Milek, Jordan Wu, Sofia Ramiro

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in 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.

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

9 authors.

Atul DeodharDivision of Arthritis and Rheumatic Diseases (OP09), Oregon Health and Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0002-2130-1246
Tae-Jong KimDepartment of Rheumatology, Chonnam National University Medical School and Hospital, Gwangju, 503-340, Republic of Korea.ORCID http://orcid.org/0000-0002-2871-1635
Victoria Navarro-CompánDepartment of Rheumatology, La Paz University Hospital, IdiPaz, Madrid, Spain.ORCID http://orcid.org/0000-0002-4527-852X
Sergio FonsecaJohnson & Johnson, Titusville, NJ, 08560, USA.ORCID http://orcid.org/0009-0008-3687-5964
José AntunesJanssen-Cilag Farmaceutica, Porto Salvo, Portugal.ORCID http://orcid.org/0000-0003-3505-6314
Arun SinghJohnson & Johnson, Titusville, NJ, 08560, USA.
Richard MilekJohnson & Johnson, 4837 DS, Breda, The Netherlands.ORCID http://orcid.org/0009-0003-4055-2686
Jordan WuJohnson & Johnson, Toronto, ON, M3C 1L9, Canada. jwu31@its.jnj.com.ORCID http://orcid.org/0009-0000-2192-338X
Sofia RamiroDepartment of Rheumatology, Leiden University Medical Center, Leiden, and Zuyderland Medical Center, Heerlen, The Netherlands.ORCID http://orcid.org/0000-0002-8899-9087

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axial spondyloarthritis is an immune-mediated inflammatory disease that primarily affects the sacroiliac joints, the spine, and the peripheral entheses and joints. The disease is associated with reduced functional ability and quality of life due to pain, fatigue, stiffness, sleep disruption, and inflammation-induced structural damage. The pathogenesis of axial spondyloarthritis involves, among other etiologies, the activation of immune-mediated proinflammatory cytokines, including tumor necrosis factor alpha, which is inhibited by golimumab, an approved treatment for the disease. Golimumab is produced using a recombinant cell line, and the antibody was derived from genetically modified mice immunized with human tumor necrosis factor alpha. This narrative review presents the primary efficacy and safety endpoints from the pivotal randomized controlled trials of golimumab. Additionally, it presents data from the post hoc analyses and real-world studies, which demonstrated benefits including decreased back pain, sleep disruption, fatigue, and disease activity as well as improved quality of life and work productivity and prolonged drug survival. Not only was golimumab associated with improvements in quality of life, general health status, and daily productivity, but a decrease in disease activity was significantly associated with these outcomes. Furthermore, golimumab was found to have a favorable safety profile, and the adverse event pattern observed was consistent with other tumor necrosis factor alpha inhibitors. Collectively, these studies showed that golimumab is an effective and safe treatment for axial spondyloarthritis.

Indexed as

Axial spondyloarthritisDrug survivalEfficacy/effectivenessGolimumabQuality of lifeSafety

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.