2004
DOI: 10.1016/j.jaad.2003.10.422
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Efficacy by clinical evaluation of imiquimod 5% cream in the treatment of superficial basal cell carcinoma: initial results from an ongoing, long-term follow-up study in Europe

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Cited by 14 publications
(12 citation statements)
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“…Imiquimod (1‐(2‐methylpropyl)‐1 H ‐imidzo[4,5‐c]quinolin‐4‐amine), a low molecular weight imidazoquinolinamines, has potent antiviral and antitumour properties and approved from Food and Drug Administration, USA 84 for the topical treatment of external anogenital warts caused by human papillomavirus (HPV) and for the skin cancers such as superficial basal cell carcinoma (BCC) and actinic keratosis in a 5% cream (Aldara) formulation 85 but during treatment permanent postinflammatory hypo‐pigmentation has been reported as a side‐effect 86 . Imiquimod is an immune response modifier and acts on the immune system by stimulating monocytes/macrophages and plasmacytoid dendritic cells in the epidermis and dermis to produce interferon‐α and other immunostimulatory cytokines that stimulate cell‐mediated immunity 87 such as macrophages and the release of oxygen‐reactive intermediates and other toxic molecules, finally leading to apoptosis of tumour cells 88 . Topical imiquimod has been found to be effective for clearing superficial BCC in 85% of cases when used 3–5 times weekly for 6 weeks, 89 and many studies have demonstrated that this regimen provides 88% histological clearance rate 84,90,91 .…”
Section: Potential Depigmenting Agentsmentioning
confidence: 99%
“…Imiquimod (1‐(2‐methylpropyl)‐1 H ‐imidzo[4,5‐c]quinolin‐4‐amine), a low molecular weight imidazoquinolinamines, has potent antiviral and antitumour properties and approved from Food and Drug Administration, USA 84 for the topical treatment of external anogenital warts caused by human papillomavirus (HPV) and for the skin cancers such as superficial basal cell carcinoma (BCC) and actinic keratosis in a 5% cream (Aldara) formulation 85 but during treatment permanent postinflammatory hypo‐pigmentation has been reported as a side‐effect 86 . Imiquimod is an immune response modifier and acts on the immune system by stimulating monocytes/macrophages and plasmacytoid dendritic cells in the epidermis and dermis to produce interferon‐α and other immunostimulatory cytokines that stimulate cell‐mediated immunity 87 such as macrophages and the release of oxygen‐reactive intermediates and other toxic molecules, finally leading to apoptosis of tumour cells 88 . Topical imiquimod has been found to be effective for clearing superficial BCC in 85% of cases when used 3–5 times weekly for 6 weeks, 89 and many studies have demonstrated that this regimen provides 88% histological clearance rate 84,90,91 .…”
Section: Potential Depigmenting Agentsmentioning
confidence: 99%
“…Hypopigmentation was reported as a side effect of treatment with imiquimod for superficial BCCs in a European Phase III study, where 44% of the subjects had mild hypopigmentation reactions and 10% of subjects experienced severe reactions. 6 One case of perma-nent facial hypopigmentation following imiquimod treatment for facial BCC was reported in the United Kingdom. 7 The pathogenesis of chemical leukoderma resulting from imiquimod is uncertain.…”
Section: Discussionmentioning
confidence: 99%
“…Imiquimod also leads to keratinocytes differentiation by activating the NOTCH pathway through the upregulation of JAGGED1 . Multiple phase III clinical trials have shown the utility of imiquimod in the initial and long‐term clearance of superficial BCCs along with favorable cosmetic outcomes . Adverse reactions associated with imiquimod include cutaneous psoriasiform eruptions, and oral ulcerations …”
Section: Interventionsmentioning
confidence: 99%