Treatment of severe psoriasis with etretin (RO 10-1670)
- PMID: 2890369
- DOI: 10.1111/j.1365-2133.1987.tb04140.x
Treatment of severe psoriasis with etretin (RO 10-1670)
Abstract
Eighty patients with severe psoriasis were treated in a double-blind fashion with either an initial dose of 10 mg, 25 mg or 50 mg of etretin daily or with placebo. Follow-up examinations were carried out monthly and the efficacy of treatment was evaluated by using the PASI score. Adverse effects of the treatment were recorded monthly; liver enzymes, cholesterol and triglycerides were measured. After 2 months of treatment the maintenance dose was reduced in some of the patients either because of complete remission or adverse effects. After 2 months treatment, groups receiving 25 mg/day and 50 mg/day showed significantly lower PASI scores than the placebo group. The 10 mg/day group showed a response intermediate between the 25 mg and 50 mg groups and the placebo group. Thus, the optimal initial dose seems to be approximately 25 mg/day and the maintenance dose somewhat lower. Six months after the start of treatment there were no significant differences between the four groups; the last follow-up examination took place during the summer and some of the patients probably experienced spontaneous improvement. Although clinical adverse effects were frequent in all groups, severe side effects, namely hair loss and paronychia, occurred frequently only among patients treated with an initial dose of 50 mg of etretin daily. The effect of treatment on liver enzymes, cholesterol and triglycerides was minimal.
Similar articles
-
Photochemotherapy for severe psoriasis without or in combination with acitretin: a randomized, double-blind comparison study.J Am Acad Dermatol. 1991 Oct;25(4):682-4. doi: 10.1016/0190-9622(91)70253-x. J Am Acad Dermatol. 1991. PMID: 1838750 Clinical Trial.
-
Etretin therapy for severe psoriasis. Evaluation of initial clinical responses.Arch Dermatol. 1987 Jan;123(1):55-8. Arch Dermatol. 1987. PMID: 2948451 Clinical Trial.
-
Acitretin improves psoriasis in a dose-dependent fashion.J Am Acad Dermatol. 1988 Apr;18(4 Pt 1):655-62. doi: 10.1016/s0190-9622(88)70086-9. J Am Acad Dermatol. 1988. PMID: 2967310 Clinical Trial.
-
Acitretin. A review of its pharmacology and therapeutic use.Drugs. 1992 Apr;43(4):597-627. doi: 10.2165/00003495-199243040-00010. Drugs. 1992. PMID: 1377120 Review.
-
Risk: benefit ratio in the treatment of psoriasis with systemic retinoids.Br J Dermatol. 1990 Jun;122 Suppl 36:135-50. doi: 10.1111/j.1365-2133.1990.tb02891.x. Br J Dermatol. 1990. PMID: 2142437 Review.
Cited by
-
Acitretin (RO10-1670) and oral contraceptives: interaction study.Arch Dermatol Res. 1988;280(6):388-9. doi: 10.1007/BF00426620. Arch Dermatol Res. 1988. PMID: 2973286 No abstract available.
-
Acitretin : A Review of its Pharmacology and Therapeutic Use.Drugs. 1992 Apr;43(4):597-627. doi: 10.2165/00003495-199243040-00010. Drugs. 1992. PMID: 28421560
-
Frizzled-related proteins 4 (SFRP4) rs1802073G allele predicts the elevated serum lipid levels during acitretin treatment in psoriatic patients from Hunan, China.PeerJ. 2018 Apr 13;6:e4637. doi: 10.7717/peerj.4637. eCollection 2018. PeerJ. 2018. PMID: 29666772 Free PMC article.
-
Fixed Tapering Dosage of Acitretin in Patients with Psoriasis: A Short-Term Analysis of Clinical Efficacy and its Effects on Biochemical Parameters.Indian J Dermatol. 2019 May-Jun;64(3):213-216. doi: 10.4103/ijd.IJD_300_18. Indian J Dermatol. 2019. PMID: 31148860 Free PMC article.
-
Adverse effects of retinoids.Med Toxicol Adverse Drug Exp. 1988 Jul-Aug;3(4):273-88. doi: 10.1007/BF03259940. Med Toxicol Adverse Drug Exp. 1988. PMID: 3054426 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials