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Comparison of Therapeutic Efficacy of Topical PUVA, Oral Etretinate, and Combined PUVA and Etretinate for the Treatment of Psoriasis and Development of PUVA Lentigines and Antinuclear Antibodies
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AbstractSixty‐two and 38 psoriatic patients were treated with topical PUVA and combined etretinate and topical PUVA (Re‐PUVA), respectively. In both groups, 50% of the patients showed initial recovery after 6 weeks and over 90% after 14 weeks. Re‐PUVA was more effective than PUVA alone in obtaining complete clearance (p<0.05). To clear psoriasis in 50% of the patients, PUVA and Re‐PUVA required 63 and 26 weeks, respectively. Furthermore, the integrated clearance rates after 70 weeks were 50% in PUVA and 63% in Re‐PUVA. Each therapy showed a similar remission period; psoriasis recurred in 50% of the patients after 4 months. In addition, 17 patients were treated with oral etretinate, and Re‐PUVA was found to be more effective than etretinate monotherapy. Another aim was to determine whether etretinate would inhibit the development of PUVA side effects. Adding etretinate failed to inhibit the production of PUVA lentigines but clearly suppressed antinuclear antibody (ANA) expression. Six of 56 patients treated with PUVA alone developed ANA during the treatment. In marked contrast (p=0.05), ANA was detected in none of 34 patients treated with Re‐PUVA.
Title: Comparison of Therapeutic Efficacy of Topical PUVA, Oral Etretinate, and Combined PUVA and Etretinate for the Treatment of Psoriasis and Development of PUVA Lentigines and Antinuclear Antibodies
Description:
AbstractSixty‐two and 38 psoriatic patients were treated with topical PUVA and combined etretinate and topical PUVA (Re‐PUVA), respectively.
In both groups, 50% of the patients showed initial recovery after 6 weeks and over 90% after 14 weeks.
Re‐PUVA was more effective than PUVA alone in obtaining complete clearance (p<0.
05).
To clear psoriasis in 50% of the patients, PUVA and Re‐PUVA required 63 and 26 weeks, respectively.
Furthermore, the integrated clearance rates after 70 weeks were 50% in PUVA and 63% in Re‐PUVA.
Each therapy showed a similar remission period; psoriasis recurred in 50% of the patients after 4 months.
In addition, 17 patients were treated with oral etretinate, and Re‐PUVA was found to be more effective than etretinate monotherapy.
Another aim was to determine whether etretinate would inhibit the development of PUVA side effects.
Adding etretinate failed to inhibit the production of PUVA lentigines but clearly suppressed antinuclear antibody (ANA) expression.
Six of 56 patients treated with PUVA alone developed ANA during the treatment.
In marked contrast (p=0.
05), ANA was detected in none of 34 patients treated with Re‐PUVA.
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