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Updated: Nov 14, 2025

Skin Biopsy for Diagnosing Discoid Lupus Erythematosus
Published on: June 10, 2025
Interventions for cutaneous disease in systemic lupus erythematosus
Cora W Hannon1, Collette McCourt2, Hermenio C Lima3
1Dermatologist, Masters of Public Health Program, Harvard School of Public Health, Boston, Massachusetts, USA.
Hydroxychloroquine, chloroquine, and methotrexate show promise for treating cutaneous lupus erythematosus (CLE). However, evidence quality is low to moderate, necessitating further research with head-to-head trials for specific CLE subtypes.
Area of Science:
- Dermatology
- Rheumatology
- Autoimmune Diseases
Background:
- Cutaneous lupus erythematosus (CLE) is a common manifestation of systemic lupus erythematosus (SLE), impacting patient morbidity.
- Various interventions exist for SLE, but their efficacy, risks, and benefits for cutaneous disease vary.
Purpose of the Study:
- To systematically assess the effects of interventions for cutaneous disease in systemic lupus erythematosus (SLE).
Main Methods:
- Conducted a comprehensive literature search across multiple databases up to June 2019, with an update in September 2020.
- Included 61 randomized controlled trials (RCTs) involving 11,232 participants, focusing on interventions for cutaneous SLE.
- Primary outcomes included complete and partial clinical response; secondary outcomes were flares and adverse events, with evidence quality assessed using GRADE.
Main Results:
- Hydroxychloroquine demonstrated probable superiority over placebo in reducing clinical flares at 6 months (moderate-quality evidence).
- Methotrexate may be superior to placebo for complete clinical response (absence of malar/discoid rash) at 6 months (low-quality evidence).
- Limited data and low-to-moderate quality evidence were noted for most comparisons, with significant risk of bias in reporting and performance/detection.
Conclusions:
- Current evidence supports hydroxychloroquine, chloroquine, and methotrexate for CLE treatment, though findings require cautious interpretation due to limited study numbers and evidence quality.
- There is a need for head-to-head intervention trials comparing treatments for specific CLE subtypes.
- Thirteen additional trials are awaiting classification and may influence future conclusions.
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