Lupus & antiphospholipid syndrome

Disease progression in patients with systemic lupus erythematosus: an analysis of the SLE Prospective Observational Cohort Study (SPOCS)

Rheumatology (Oxford)Published Prospective observational cohort study

Authors' conclusion

In the SPOCS cohort, disease activity was stable or reduced over time, but treatment target attainment was low and organ damage increased. At month 36, there were no clear differences by baseline IFNGS.

Study context

Population
Adults with moderate to severe SLE activity receiving standard of care750 with IFN gene signature (IFNGS) status
Participants
826 adults
Exposure
IFNGS-high vs IFNGS-low at baseline
  • IFNGS-highn = 531
  • IFNGS-lown = 219reference
Outcome
Disease progression (SLEDAI-2K, PGA, SELENA-SLEDAI flares, SLICC/ACR DI, DORIS remission/LLDAS) by baseline IFNGS
Follow-up
≤36 months
Methodological detailsbiannual assessments for ≤36 months
  • Biannual assessments for ≤36 months

Main finding

As reported in the abstract

Disease progression over 36 months · month 36

SLEDAI-2K decreased from baseline to month 36, regardless of baseline IFNGS

9.8 ± 4.6-5.7 ± 7.7

≥1 flare by month 36

44.7%

183/409

Definition of Remission in SLE (DORIS) remission attained at any timepoint

<15%

Lupus Low Disease Activity State (LLDAS) attained at any timepoint

<20%

Observational data: associations, not effects.

Further findings

Baseline characteristics: age (years) and GC use · events/value = GC use

Age, mean ± SD (years) IFNGS-high 42.9 ± 13.6 · IFNGS-low 50.8 ± 12.9

Baseline characteristics: age (years) and GC use — Time since SLE diagnosis, mean ± SD (years)
11.1 ± 9.2
Baseline characteristics: age (years) and GC use — IFNGS-high at enrolment
70.8% (531/750)

Original publication

Disease progression in patients with systemic lupus erythematosus: an analysis of the SLE Prospective Observational Cohort Study (SPOCS). Rheumatology (Oxford). Published 11 November 2025. doi:10.1093/rheumatology/keaf599

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