Chemical structure of cidofovir
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Cidofovir

Cidofovir is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis in patients with AIDS. It suppresses CMV replication by selective inhibition of viral DNA synthesis. more...

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Cidofovir demonstrated a statistically significant effect in delaying the progression of CMV retinitis lesions in newly diagnosed patients, as well as in previously treated patients who had failed other therapies. Maintenance therapy with cidofovir involves an infusion only once every two weeks, making it a convenient treatment option. Because dosing is relatively infrequent, a permanent catheter is not necessary for infusions.

Cidofovir has also been investigated as a treatment for progressive multifocal leukoencephalopathy, but as of 2005 studies are inconclusive.

Cidofovir was developed by Gilead Sciences and is marketed with the brand name Vistide by Gilead in the USA, and by Pfizer elsewhere.


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Clinical clearance of basal cell carcinoma with topical cidofovir - Washington Whispers - Brief Article
From Journal of Drugs in Dermatology, 4/1/03

In this case report, four patients are described with basal cell carcinomas (BCC) treated with 1% topical cidofovir. Cidofovir is a purine nucleotide analog, effective against a wide number of DNA viruses. However, this drug may also have antineoplastic properties, presumably through the induction of apoptosis and inhibition of angiogenesis. Although surgical excision is traditionally the treatment of choice in patients presenting with basal cell carcinomas, this option may not be amenable to all patients for a variety of reasons. Four patients are described who refused surgery for their basal cell carcinomas. Two of the patients had lesions on their faces, one had a large (10 x 14 mm) BCC on the side of his head, and one patient had a BCC on her sternum. 1% cidofovir was applied daily for 10 days, then every other day for another 50 days. All patients experienced local reactions at the site of application: erythema, itching, and erosion. All patients achieved complete clinical regression (up to 24 months) of their BCC after treatment. Three of the patients underwent biopsies which showed histopathologic clearing 3 months after the end of therapy. The patient with the large lesion on the side of his head subsequently underwent complete excision (despite clinical clearance) and the histopathology showed tumor cells with numerous apoptotic bodies and an intense lymphocytic infiltrate. The authors point out that although the number of patients treated was small, this experience shows the potential effectiveness of 1% cidofovir in the non-surgical treatment of BCCs.

Donato Calista. Topical 1% Cidofovir for the Treatment of Basal Cell Carcinoma. European Journal of Dermatology 2002; 12:562-4.

COPYRIGHT 2003 Journal of Drugs in Dermatology
COPYRIGHT 2003 Gale Group

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