Evidence map›Paper›PMID 39855677›Full record

Observational studyLupus science & medicine2025

Real-world treatment patterns and clinical characteristics in patients with moderate-to-severe systemic lupus erythematosus: an analysis of the SLE Prospective Observational Cohort Study (SPOCS).

Martin Aringer, Laurent Arnaud, Richard A Furie, Eric F Morand, Christine Peschken, Alberta Hoi, Barnabas Desta, Jonatan Hedberg, Tina Grünfeld Eén, Alessandro Sorrentino and 4 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03189875 (Systemic Lupus Erythematosus), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT03189875 completednot on this map

Systemic Lupus Erythematosus (SLE) Prospective Observational Cohort Study (SPOCS): Prospective Observational Cohort of Patients With Moderate-to-severe SLE to Characterize Cross-sectional and Longitudinal Disease Activity, Treatment Patterns and Effectiveness, Outcomes and Comorbidities, Healthcare Resource Utilization, and the Impact of SLE on Quality of Life by Type I Interferon Expression

TypeobservationalSponsorAstraZenecaRan2017 to 2022Enrolled830ConditionsSystemic Lupus ErythematosusArmsStandard of Care
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. 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

14 authors.

Martin AringerInternal Medicine III, TU Dresden, Dresden, Germany.ORCID 0000-0003-4471-8375
Laurent ArnaudDepartment of Rheumatology, Hôpitaux universitaires de Strasbourg, Strasbourg, France.ORCID 0000-0002-8077-8394
Richard A FurieNorthwell Health, New Hyde Park, New York, USA.
Eric F MorandMonash University, Melbourne, Victoria, Australia.ORCID 0000-0002-9507-3338
Christine PeschkenUniversity of Manitoba, Winnipeg, Manitoba, Canada.
Alberta HoiMonash University, Melbourne, Victoria, Australia.ORCID 0000-0002-9416-7383
Barnabas DestaBioPharmaceuticals R&D, AstraZeneca US, Gaithersburg, Maryland, USA.
Jonatan HedbergBioPharmaceuticals Medical, AstraZeneca, Gothenburg, Sweden.
Tina Grünfeld EénBioPharmaceuticals Medical, AstraZeneca, Gothenburg, Sweden.
Alessandro SorrentinoAstraZeneca PLC, Cambridge, UK.
Danuta KielarAstraZeneca PLC, Cambridge, UK.
Raj TummalaBioPharmaceuticals R&D, AstraZeneca US, Gaithersburg, Maryland, USA.
Stephanie ChenBioPharmaceuticals Medical, AstraZeneca US, Gaithersburg, Maryland, USA.
Bo DingBioPharmaceuticals Medical, AstraZeneca, Gothenburg, Sweden Bo.Ding@astrazeneca.com.ORCID 0000-0001-9131-4563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSystemic lupus erythematosus (SLE) is a disease with heterogeneous treatment patterns largely based on organ involvement and disease severity. The SLE Prospective Observational Cohort Study (SPOCS) collected data worldwide over 3 years from patients with moderate-to-severe SLE. We report real-world patterns of medication use in patients enrolled in SPOCS.

methodsData were collected at study entry; patients were followed twice annually according to local practice. Disease activity (SLE Disease Activity Index 2000 (SLEDAI-2K)), average oral glucocorticoid dose and use of other treatments-specifically antimalarials, biologics and immunosuppressants-were measured over time. Subgroup analyses were stratified by baseline interferon gene signature (IFNGS) status and disease activity (SLEDAI-2K) status.

resultsPatient demographics and baseline characteristics were similar among subgroups; the majority of patients were on antimalarials (n=670; 81.1%), followed by glucocorticoids (n=537; 65.0%), immunosuppressants (n=453; 54.8%) and biologics (n=175; 21.2%). In the overall population, median (IQR) SLEDAI-2K scores decreased within 12 months (baseline: 8.0 (6.0-12.0); 12 months: 4.0 (2.0-8.0)) and remained stable thereafter. The mean (SD) daily oral glucocorticoid dose increased by 6 months (baseline: 6.0 (7.09); 6 months: 9.8 (8.67)) and remained stable thereafter. The proportion of patients who were on glucocorticoid doses >5 mg/day ranged from ~20% to 33% throughout the study. In subgroup analyses, patients with high IFNGS and high disease activity state (HDAS) at baseline used more immunosuppressants and glucocorticoids compared with those with low IFNGS and non-HDAS at baseline.

conclusionsThese findings underscore that SLE therapy is still often unable to reach goals as recommended by the European Alliance of Associations for Rheumatology, both with regard to glucocorticoid use and disease activity, suggesting that there is an unmet need for new treatment options for patients with SLE. TRIAL REGISTRATION NUMBER: NCT03189875; 16 June 2017.

Indexed as

AntimalarialsGlucocorticoidsImmunosuppressive AgentsLupus Erythematosus, SystemicAdultBiological ProductsFemaleHumansInterferonsMaleMiddle AgedProspective StudiesSeverity of Illness IndexAntimalarialsBiological ProductsGlucocorticoidsImmunosuppressive AgentsInterferonsAutoimmune DiseasesEpidemiologyGlucocorticoidsLupus Erythematosus, SystemicTherapeutics

Identifiers

PMID39855677
PMCPMC11881029

What OpenQuestion holds

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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.