Evidence map›Paper›PMID 41207318›Full record

ReviewThe Lancet. Respiratory medicine2026

A paradigm shift in corticosteroid therapy for sarcoidosis: a World Association of Sarcoidosis and Other Granulomatous Disorders Position Paper, endorsed by the Americas Association of Sarcoidosis and Other Granulomatous Disorders.

Athol U Wells, Elyse E Lower, Robert P Baughman, Daniel A Culver, Marc A Judson, Catherine A Bonham, Alicia K Gerke, Jan C Grutters, Chris Knoet, Filippo Martone and 4 more

Abstract readReview
In one paragraph

Review in The Lancet. Respiratory medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Advances in management of sarcoidosis-associated fatigue: A narrative review.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2026
    Article
  7. New Therapies for Sarcoidosis: Molecular and Pathophysiological Basis.International journal of molecular sciences · 2026
    Review
  8. Contemporary management of sarcoidosis.Frontiers in medicine · 2026
    Review
  9. Advanced Pulmonary Sarcoidosis: Treatment and Monitoring.Diagnostics (Basel, Switzerland) · 2025
    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

14 authors.

Athol U WellsDepartment of Respiratory Medicine, Royal Brompton Hospital, London, UK; Margaret Turner-Warwick Centre, Imperial College, London, UK. Electronic address: atholumfrey.wells@nhs.net.
Elyse E LowerDepartment of Medicine, University of Cincinnati, Cincinnati, OH, USA.
Robert P BaughmanDepartment of Medicine, University of Cincinnati, Cincinnati, OH, USA.
Daniel A CulverDepartment of Pulmonary Medicine, Cleveland Clinic, Cleveland, OH, USA.
Marc A JudsonAlbany Medical College, Albany, NY, USA.
Catherine A BonhamSarcoidosis and Interstitial Lung Disease Center of Excellence, University of Virginia, Charlottesville, VA, USA.
Alicia K GerkeIowa River Landing and Medical Center, Iowa City, IA, USA; Department of Internal Medicine, University of Iowa, IA, USA.
Jan C GruttersUniversity Medical Centre and St Antonius Hospital, Utrecht, Netherlands.
Chris KnoetEuropean Lung Foundation, Sheffield, UK.
Filippo MartoneEuropean Lung Foundation, Sheffield, UK.
Katja SchillhornEuropean Lung Foundation, Sheffield, UK.
John H StoneHarvard Medical School, Boston, MA, USA; Department of Clinical Rheumatology, Massachusetts General Hospital, Boston, MA, USA.
Andrea B WilsonFoundation of Sarcoidosis Research, Chicago, IL, USA.
Elliott D CrouserCenter for Clinical and Translational Science, Ohio State University, OH, USA; Ohio State University Wexner Medical Center, Columbus, OH, USA.

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Modeling to Design Treatments for Idiopathic Lung FibrosisR01HL155143 · NHLBI · UNIVERSITY OF VIRGINIA · PI BARKER, THOMAS HARRISON, PEIRCE-COTTLER, SHAYN · 2021 to 2024
$2.2M
NHLBI NIH HHS R01 HL155143NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

For over seven decades, oral corticosteroids have been the cornerstone of sarcoidosis management. Oral corticosteroids suppress sarcoidosis inflammation rapidly, but long-term oral corticosteroids result in toxicity and some patients are unable to taper oral corticosteroids without experiencing disease flare ups. The routine use of oral corticosteroids as first-line therapy, as recommended in sarcoidosis guidelines, could have unintentionally promoted the long-term use of oral corticosteroids. We believe that oral corticosteroids should no longer be considered as first-line therapy in all patients with sarcoidosis requiring treatment. Furthermore, we view long-term use of oral corticosteroids in sarcoidosis as an undesirable outcome. When initial oral corticosteroids are required, we propose that oral corticosteroids be used as bridging therapy, ideally for no longer than 3-4 months. There is an urgent need to address the widespread use of long-term maintenance therapy with oral corticosteroids in patients with sarcoidosis, and we advocate the systematic withdrawal of steroid therapy with replacement, if necessary, by other immunosuppressive agents.

Indexed as

Adrenal Cortex HormonesGlucocorticoidsSarcoidosisAdministration, OralHumansImmunosuppressive AgentsPractice Guidelines as TopicAdrenal Cortex HormonesGlucocorticoidsImmunosuppressive Agents

Identifiers

PMID41207318
PMCPMC13397509

What OpenQuestion holds

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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.