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Long-term continuous versus intermittent cyclosporin: therapy for psoriasis
Mamitaro Ohtsuki1, Hidemi Nakagawa, Junichi Sugai
1Jichi Medical School, Tochigi, Japan.
The Journal of Dermatology
|April 23, 2003
Summary
Long-term cyclosporin A (CyA) therapy for psoriasis shows similar efficacy with continuous and intermittent regimens. Intermittent therapy may be safer due to potential cancer risks with continuous CyA, though further research is needed.
Area of Science:
- Dermatology
- Immunosuppressive Therapy
Background:
- Psoriasis is a chronic inflammatory skin condition requiring long-term management.
- Cyclosporin A (CyA) is an effective immunosuppressant for moderate to severe psoriasis.
- Optimal long-term dosing strategies for CyA in psoriasis remain under investigation.
Purpose of the Study:
- To compare the long-term efficacy and safety of continuous versus intermittent cyclosporin A (CyA) regimens for psoriasis.
- To evaluate adverse events and disease control over an extended follow-up period.
Main Methods:
- A multicenter randomized controlled study followed 31 psoriasis patients for at least 48 months.
- Patients received either continuous CyA therapy or intermittent CyA with topical corticosteroids.
- Psoriasis Area and Severity Index (PASI) scores and adverse events were monitored.
Main Results:
- Both continuous and intermittent CyA regimens significantly reduced PASI scores by over 70% from baseline.
- Long-term PASI scores were maintained between 5-12 points for both groups, with no significant difference in response rates.
- Continuous therapy showed slightly better overall psoriasis control, but intermittent therapy had fewer reported malignancies and renal impairment in elderly patients.
Conclusions:
- Cyclosporin A demonstrates long-term efficacy and tolerability for psoriasis under both continuous and intermittent regimens.
- Intermittent therapy may be preferable due to potential malignancy risks associated with continuous CyA, despite slightly lower efficacy.
- Further research is needed to optimize intermittent CyA protocols for safety and efficacy comparable to continuous therapy.