2015
DOI: 10.1136/sextrans-2014-051810
|View full text |Cite
|
Sign up to set email alerts
|

Imiquimod 5% cream for five consecutive days a week in an HIV-infected observational cohort up to 32 weeks in the treatment of high-grade squamous intraepithelial lesions: Table 1

Abstract: Topical imiquimod 5% cream is useful in HSIL. A five consecutive days treatment regimen with imiquimod 5% cream for HSIL does not seem to be more effective compared with the customary prescription for 3 days a week. A prolonged course of imiquimod 5% cream is warranted for intra-anal HSIL. Adverse effects are comparable between 3 and 5 days treatment regimen.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
16
0
1

Year Published

2015
2015
2021
2021

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 22 publications
(17 citation statements)
references
References 10 publications
(11 reference statements)
0
16
0
1
Order By: Relevance
“…12,13,[15][16][17][18][19] However, in most studies, patients with condylomas and low-and high-grade dysplasia at both intra-anal and perianal sites have been analyzed together, making it hard to draw firm conclusions on efficacy. 12,13,[15][16][17][18]20,21 Previously reported response rates to imiquimod for the treatment of any degree of anal dysplasia (AIN-1-3) vary within a wide range from 35 to 68%. 12,13,[16][17][18] In contrast, the current study shows a relatively lower CR rate (approximately 4%) which is likely related to the strict inclusion criteria limited to HSIL.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…12,13,[15][16][17][18][19] However, in most studies, patients with condylomas and low-and high-grade dysplasia at both intra-anal and perianal sites have been analyzed together, making it hard to draw firm conclusions on efficacy. 12,13,[15][16][17][18]20,21 Previously reported response rates to imiquimod for the treatment of any degree of anal dysplasia (AIN-1-3) vary within a wide range from 35 to 68%. 12,13,[16][17][18] In contrast, the current study shows a relatively lower CR rate (approximately 4%) which is likely related to the strict inclusion criteria limited to HSIL.…”
Section: Discussionmentioning
confidence: 99%
“…12,13,[15][16][17][18][19] Their results should be cautiously interpreted since the majority of them have analyzed heterogeneous cohorts of patients. 12,13,[15][16][17][18]20,21 Despite a large number of publications on imiquimod efficacy in the treatment of external genital and perianal warts, [22][23][24][25] safety and efficacy data for the treatment of intra-anal condylomas has rarely been evaluated. 14,20,26 Furthermore, data regarding the tolerability profile of topical imiquimod for treating anal HPV-associated pathology are also very limited.…”
Section: Introductionmentioning
confidence: 99%
“…Это связано либо с высокой частотой рецидивирования (аногенитальные бородавки), склонностью к малигнизации (плоскоклеточный рак кожи) или быстро формирующейся резистентностью к противовирусным препаратам (ВПГ). В этих ситуациях имихимод может стать дополнительной альтернативой недостаточно эффективной или совсем неэффективной терапии [8,24,25], что особенно актуально при лечении атипичных форм генитального герпеса у ВИЧ-инфицированных больных, для которых характерны торпидное течение, высокий риск рецидивов и множественная лекарственная устойчивость [25].…”
Section: результатыunclassified
“…Imiquimod is a drug with anticarcinogenic and antiviral activity, and it is recommended for treatment of genital/perianal condylomas. It is not suggested for the treatment of anal HSIL; nevertheless, the results of two research studies about imiquimod in premalignant anal lesions in HIV-positive patients have been published with a cure rate of 45 to 61% [1,2]. The aim of this prospective study was to analyze the efficacy of 3 consecutive days a week for 4 months of self-administered treatment with imiquimod 5% cream for anal HSIL, and to assess safety, and antiviral activity against HPV, in seropositive patients.…”
mentioning
confidence: 99%