Evidence map›Paper›PMID 29382380›Full record

ArticleArthritis research & therapy2018

Systemic sclerosis associated interstitial lung disease - individualized immunosuppressive therapy and course of lung function: results of the EUSTAR group.

Sabine Adler, Dörte Huscher, Elise Siegert, Yannick Allanore, László Czirják, Francesco DelGaldo, Christopher P Denton, Oliver Distler, Marc Frerix, Marco Matucci-Cerinic and 7 more

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
–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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Guideline
  3. Trial
  4. Trial
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. CD19 + CD21Clinical and experimental medicine · 2022
    Article
  16. Review
  17. Article
  18. Immunosuppression use in early systemic sclerosis may be increasing over time.Journal of scleroderma and related disorders · 2022
    Article
  19. Article
  20. 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

17 authors.

Sabine AdlerDepartment of Rheumatology, Immunology and Allergology, University Hospital and University of Bern, Freiburgstrasse 4, 3010, Bern, Switzerland. sabine.adler@insel.ch.
Dörte HuscherGerman Rheumatism Research Center, A Leibniz Institute, Berlin, Germany.
Elise SiegertDepartment of Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany.
Yannick AllanoreDepartment of Rheumatology A, Descartes University, APHP, Cochin Hospital, Paris, France.
László CzirjákDepartment of Rheumatology and Immunology, University of Pecs, Pecs, Hungary.
Francesco DelGaldoUniversity of Leeds, Leeds, UK.
Christopher P DentonUCL Division of Medicine, Centre for Rheumatology, Royal Free Hospital, London, UK.
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.
Marc FrerixDepartment of Rheumatology and Clinical Immunology, Osteology and Physical Therapy, Justus-Liebig-University Giessen, Kerckhoff Klinik, Bad Nauheim, Germany.
Marco Matucci-CerinicDepartment Experimental and Clinical Medicine, Division of Rheumatology AOUC, University of Florence, Florence, Italy.
Ulf Mueller-LadnerDepartment of Rheumatology and Clinical Immunology, Osteology and Physical Therapy, Justus-Liebig-University Giessen, Kerckhoff Klinik, Bad Nauheim, Germany.
Ingo-Helmut TarnerDepartment of Rheumatology and Clinical Immunology, Osteology and Physical Therapy, Justus-Liebig-University Giessen, Kerckhoff Klinik, Bad Nauheim, Germany.
Gabriele ValentiniDepartment of Rheumatology, Second University of Naples, Naples, Italy.
Ulrich A WalkerDepartment of Rheumatology, University of Basel, Basel, Switzerland.
Peter M VilligerDepartment of Rheumatology, Immunology and Allergology, University Hospital and University of Bern, Freiburgstrasse 4, 3010, Bern, Switzerland.
Gabriela RiemekastenDepartment of Rheumatology, University Medical Center Schleswig-Holstein, Kiel, Germany.
EUSTAR co-workers on behalf of the DeSScipher project research group within the EUSTAR network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterstitial lung disease in systemic sclerosis (SSc-ILD) is a major cause of SSc-related death. Imunosuppressive treatment (IS) is used in patients with SSc for various organ manifestations mainly to ameliorate progression of SSc-ILD. Data on everyday IS prescription patterns and clinical courses of lung function during and after therapy are scarce.

methodsWe analysed patients fulfilling American College of Rheumatology (ACR)/European League against Rheumatism (EULAR) 2013 criteria for SSc-ILD and at least one report of IS. Types of IS, pulmonary function tests (PFT) and PFT courses during IS treatment were evaluated.

resultsEUSTAR contains 3778/11,496 patients with SSc-ILD (33%), with IS in 2681/3,778 (71%). Glucocorticoid (GC) monotherapy was prescribed in 30.6% patients with GC combinations plus cyclophosphamide (CYC) (11.9%), azathioprine (AZA) (9.2%), methotrexate (MTX) (8.7%), or mycophenolate mofetil (MMF) (7.3%). Intensive IS (MMF + GC, CYC or CYC + GC) was started in patients with the worst PFTs and ground glass opacifications on imaging. Patients without IS showed slightly less worsening in forced vital capacity (FVC) when starting with FVC 50-75% or >75%. GC showed negative trends when starting with FVC <50%. Regarding diffusing capacity for carbon monoxide (DLCO), negative DLCO trends were found in patients with MMF.

conclusionsIS is broadly prescribed in SSc-ILD. Clusters of clinical and functional characteristics guide individualised treatment. Data favour distinguished decision-making, pointing to either watchful waiting and close monitoring in the early stages or start of immunosuppressive treatment in moderately impaired lung function. Advantages of specific IS are difficult to depict due to confounding by indication. Data do not support liberal use of GC in SSc-ILD.

Indexed as

AdultAgedCyclophosphamideDrug Therapy, CombinationFemaleHumansImmunosuppressive AgentsLungLung Diseases, InterstitialMaleMethotrexateMiddle AgedMycophenolic AcidPrecision MedicineRespiratory Function TestsScleroderma, SystemicCyclophosphamideImmunosuppressive AgentsMethotrexateMycophenolic AcidFollow upImmunosuppressantsInterstitial lung diseaseLung functionSystemic sclerosis

Identifiers

PMID29382380
PMCPMC5791165

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.