Initial hydroxychloroquine monotherapy in systemic lupus erythematosus: report of three cases.
Kento IchikawaYohei KirinoYosuke KunishitaDaiga KishimotoKaoru Takase-MinegishiRyusuke YoshimiHideaki NakajimaPublished in: Modern rheumatology case reports (2021)
Glucocorticoids (GCs) use is associated with increased organ damage in systemic lupus erythematosus (SLE), and the treatment goal is to stop their use. Treatment with hydroxychloroquine (HCQ) without daily GCs may benefit patients by minimising the cumulative dose of GCs, but clinical experience with HCQ monotherapy is limited. To accumulate evidence for initial HCQ monotherapy in SLE, we retrospectively analysed three new SLE patients who visited Yokohama City University Hospital in 2015. The patients were all Japanese females with a mean age of 26.0 ± 5.3 years, high anti-dsDNA antibody titres, no major organ damage, and a mean pre-treatment Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score of 9.3 ± 3.1. During the mean observation period of 3.8 ± 0.8 years, none of them received daily GCs or immunosuppressants, but one of the three patients were treated with short-term oral GCs and NSAIDs for a skin rash or arthralgia flairs. SLEDAI-2K was reduced to 3.3 ± 1.2. No other new SLE symptoms emerged, and the Systemic Lupus International Collaborating Clinics Damage Index (SDI) of them were maintained at 0. None of the patients developed HCQ-related retinal toxicity. Current experience with initial HCQ monotherapy suggests that such a therapeutic strategy may be useful in managing disease activity and preserving cumulative GCs in SLE patients without organ involvements.
Keyphrases
- peritoneal dialysis
- end stage renal disease
- systemic lupus erythematosus
- disease activity
- rheumatoid arthritis
- randomized controlled trial
- rheumatoid arthritis patients
- oxidative stress
- combination therapy
- chronic kidney disease
- ejection fraction
- primary care
- newly diagnosed
- clinical trial
- ankylosing spondylitis
- optical coherence tomography
- juvenile idiopathic arthritis
- replacement therapy
- double blind
- patient reported outcomes