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1.
Antimicrob Agents Chemother ; 42(4): 789-94, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9559784

RESUMO

Genital human papillomavirus infection is one of the most common sexually transmitted diseases. Imiquimod is a new agent, an immune-response modifier, that has been demonstrated to have potent in vivo antiviral and antitumor effects in animal models. The present prospective, multicenter, double-blind, randomized, vehicle-controlled trial evaluated the efficacy and safety of daily patient-applied imiquimod for up to 16 weeks for the treatment of external genital warts. Wart recurrence was investigated during a 12-week treatment-free follow-up period. In the intent-to-treat analysis, baseline warts cleared from 49 of 94 (52%) patients treated with 5% imiquimod cream, 13 of 90 (14%) patients treated with 1% imiquimod cream, and 3 of 95 (4%) vehicle-treated patients; the differences between the groups treated with vehicle and imiquimod were significant (P < 0.0001). For subjects who completed the follow-up period, recurrence rates after a complete response were 19% (9 of 48 patients) in the 5% imiquimod cream group, 17% (2 of 12) in the 1% imiquimod cream group, and 0% (0 of 3) in the vehicle-treated group. There were no systemic reactions, although local skin reactions (generally of mild or moderate severity) were common, particularly in the 5% imiquimod cream group. Local reactions caused two patients to discontinue treatment. The most frequently reported local skin reactions were erythema, excoriation or flaking, and erosion. Patient-applied 5% imiquimod cream is effective for the treatment of external genital warts and has a favorable safety profile.


Assuntos
Aminoquinolinas/uso terapêutico , Condiloma Acuminado/tratamento farmacológico , Indutores de Interferon/uso terapêutico , Papillomaviridae , Administração Tópica , Adolescente , Adulto , Aminoquinolinas/administração & dosagem , Aminoquinolinas/efeitos adversos , Condiloma Acuminado/patologia , Método Duplo-Cego , Feminino , Humanos , Imiquimode , Indutores de Interferon/administração & dosagem , Indutores de Interferon/efeitos adversos , Masculino , Recidiva
2.
Arch Dermatol ; 134(1): 25-30, 1998 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9449906

RESUMO

OBJECTIVE: To compare the safety and effectiveness of 5% and 1% imiquimod cream with vehicle cream in the treatment of external anogenital warts. DESIGN: Randomized, double-blind, placebo-controlled comparison that evaluated patients for total clearance of their warts. Patients who experienced total clearance were evaluated for recurrence in a 12-week follow-up. SETTING: Eleven ambulatory offices, including both private physician offices and referral medical centers. PATIENTS: Three hundred eleven healthy men and women aged 18 years or older with 2 to 50 external anogenital warts were recruited from the practices of investigators, referring physicians, and advertisements. Eighty-two additional patients were screened but did not qualify. Four patients discontinued use of the medication because of adverse effects. INTERVENTIONS: Five percent imiquimod (Aldara) cream, 1% imiquimod cream, or vehicle cream was applied to all external warts overnight 3 times each week for 16 weeks, or until all treated warts disappeared, whichever occurred first. MAIN OUTCOME MEASUREMENTS: The number of patients experiencing the elimination of all baseline warts and the recurrence rate of these warts. In addition, the reduction in baseline wart area the duration of therapy required to eliminate warts, and the frequency and severity of adverse reactions were principal measurements. RESULTS: In the intent-to-treat analysis, 54 (50%) of 109 patients who received 5% imiquimod cream, 21 (21%) of 102 of those who received 1% imiquimod cream, and 11 (11%) of 100 patients treated with vehicle cream experienced eradication of all treated baseline warts. The difference between the effectiveness of 5% imiquimod cream and the vehicle cream was statistically significant (P < .001). Of those patients whose warts cleared during therapy, 13% of patients who received 5% imiquimod experienced a recurrence of at least 1 wart. Recurrences occurred in none of the patients who used 1% imiquimod cream and in 10% of patients who used the vehicle cream. Local erythema was the most common adverse reaction, but the majority of patients in each group experienced no or only mild local inflammatory reactions. There were no differences in incidences of flulike symptoms among treatment groups. CONCLUSIONS: Five percent imiquimod cream is an effective and safe self-administered therapy for external anogenital warts when applied 3 times a week overnight for up to 16 weeks. The recurrence rate is low.


Assuntos
Adjuvantes Imunológicos/uso terapêutico , Aminoquinolinas/uso terapêutico , Doenças do Ânus/terapia , Condiloma Acuminado/terapia , Doenças dos Genitais Femininos/terapia , Doenças dos Genitais Masculinos/terapia , Indutores de Interferon/uso terapêutico , Adjuvantes Imunológicos/administração & dosagem , Adjuvantes Imunológicos/efeitos adversos , Administração Cutânea , Adulto , Aminoquinolinas/administração & dosagem , Aminoquinolinas/efeitos adversos , Dermatite/etiologia , Método Duplo-Cego , Esquema de Medicação , Eritema/etiologia , Feminino , Seguimentos , Humanos , Imiquimode , Incidência , Indutores de Interferon/administração & dosagem , Indutores de Interferon/efeitos adversos , Masculino , Pomadas , Veículos Farmacêuticos , Placebos , Recidiva , Indução de Remissão , Segurança , Autoadministração , Resultado do Tratamento
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