Evidence map›Paper›PMID 40065521›Full record

ArticleACR open rheumatology2025

Comparative Efficacy of Immunosuppressive Therapies in the Treatment of Diffuse Cutaneous Systemic Sclerosis.

Barbara White, Daniel E Furst, Tracy M Frech, Masataka Kuwana, Laura Hummers, Wendy Stevens, Suzanne Kafaja, Eun Bong Lee, Oliver Distler, Dinesh Khanna and 3 more

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Review
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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

13 authors.

Barbara WhiteCorbus Pharmaceuticals Holdings Inc, Norwood, Massachusetts, USA (current address: SFJ Pharmaceuticals, Inc, Pleasanton, California, USA).
Daniel E FurstUniversity of California, Los Angeles.
Tracy M FrechVanderbilt University, Nashville, Tennessee.ORCID https://orcid.org/0000-0002-5472-3840
Masataka KuwanaNippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8352-6136
Laura HummersJohns Hopkins University, Baltimore, Maryland.ORCID https://orcid.org/0000-0002-4864-4011
Wendy StevensUniversity of Melbourne, Melbourne, Victoria, Australia.
Suzanne KafajaUniversity of California, Los Angeles.
Eun Bong LeeSeoul National University, Seoul, South Korea.ORCID https://orcid.org/0000-0003-0703-1208
Oliver DistlerUniversity Hospital Zürich, Zürich, Switzerland.ORCID https://orcid.org/0000-0002-0546-8310
Dinesh KhannaUniversity of Michigan, Ann Arbor.ORCID https://orcid.org/0000-0003-1412-4453
Christopher P DentonUniversity College London, London, United Kingdom.ORCID https://orcid.org/0000-0003-3975-8938
Robert SpieraHospital for Special Surgery, New York, New York.ORCID https://orcid.org/0000-0003-2911-6800
RESOLVE‐1 investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe RESOLVE-1 trial of lenabasum in diffuse cutaneous systemic sclerosis (dcSSc) allowed background immunosuppressive therapy (IST) at the discretion of individual investigators, and no significant differences were observed between treatment arms. This provides a powerful opportunity to compare the relative efficacy of different ISTs in a well-defined large cohort of patients with dcSSc.

methodsPrespecified IST categories, efficacy end points, baseline disease characteristics likely to influence efficacy outcomes, the definition of interstitial lung disease, definitions of IST use, and categories of IST use by which efficacy outcomes were evaluated were. Descriptive statistics are used to present results.

resultsFor skin, change in modified Rodnan skin score (mRSS) was numerically greatest with mycophenolate mofetil (MMF) treatment in patients with the earliest disease, reaching -10.8 points in the MMF group versus -4.8 points in the no IST group in patients with a disease duration ≤2 years. Other ISTs had improvements intermediate between that seen in the MMF and no IST groups. Forced vital capacity (mL) was stable over 52 weeks in patients in the MMF group compared to an around 160-mL decline over 52 weeks in no IST group. Differences in outcome were observed between antinuclear antibody subgroups, with greater difference in favor of MMF for skin and lungs being observed in anti-topoisomerase 1 autoantibody-positive patients. In contrast, anti-RNA polymerase III autoantibody-positive patients in both the no IST and MMF groups improved rapidly, with a decrease in mRSS.

conclusionTaken together, our findings robustly support routine use of MMF in dcSSc and show benefit especially in early-stage disease. Those patients with high-risk antibodies for lung fibrosis might be especially suitable for MMF treatment.

Identifiers

PMID40065521
PMCPMC11893482

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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.