The antiviral drug docosanol as a treatment for Kaposi's sarcoma lesions in HIV type 1-Infected patients: A pilot clinical study

Citation
Mj. Scolaro et al., The antiviral drug docosanol as a treatment for Kaposi's sarcoma lesions in HIV type 1-Infected patients: A pilot clinical study, AIDS RES H, 17(1), 2001, pp. 35-43
Citations number
32
Categorie Soggetti
Immunology
Journal title
AIDS RESEARCH AND HUMAN RETROVIRUSES
ISSN journal
08892229 → ACNP
Volume
17
Issue
1
Year of publication
2001
Pages
35 - 43
Database
ISI
SICI code
0889-2229(20010101)17:1<35:TADDAA>2.0.ZU;2-8
Abstract
Docosanol inhibits a broad spectrum of lipid-enveloped viruses ill vitro in cluding HSV-1, HSV-2, VZV, CMV, HHV-6, and HIV-1. These observations led us to conduct a pilot clinical study with docosanol 10% cream as a topical tr eatment for Kaposi's sarcoma (KS) in HIV-1-infected patients. In this open- label study 28 cutaneous KS lesions in 10 HIV-1-infected patients were trea ted topically five times daily for 4 weeks with evaluation of lesion charac teristics of area, edema, and color. All patients elected to enroll in an e xtended treatment protocol and continued to treat for up to 35 weeks. Withi n 28 days, 2 of 10 patients exhibited a partial response based on standardi zed criteria exhibiting 74 to 83% reductions in total target lesion areas. With extended treatment, a partial response was exhibited in two additional patients where total target lesion area was reduced by 52% in one patient and target lesions in another patient that had been large, swollen, and pai nful at study initiation were no longer visible. No patient experienced dis ease progression or signs of visceral disease. The average percent decrease in lesion area for all target lesions was 20% (p < 0.01). A patient's resp onse to therapy appeared to be independent of anti-HIV regimen, HIV viral l oad, or previous KS treatments. These results suggest that docosanol merits further investigation as a potential topical therapy in the treatment of A IDS-associated Kaposi's sarcoma lesions.