Safety and efficacy of pegylated liposomal doxorubicin in HIV-associated Kaposi’s sarcoma
Identifieur interne : 006044 ( Main/Exploration ); précédent : 006043; suivant : 006045Safety and efficacy of pegylated liposomal doxorubicin in HIV-associated Kaposi’s sarcoma
Auteurs : Francesca Cainelli [Botswana] ; Alfredo Vallone [Italie]Source :
- Biologics : Targets & Therapy [ 1177-5475 ] ; 2009.
Abstract
Kaposi’s sarcoma is a vascular tumor linked to the presence of Kaposi’s sarcoma-associated herpesvirus (human herpesvirus-8) and the incidence of which has increased considerably the world over after the onset of the human immunodeficiency virus (HIV) pandemic. Antiretroviral therapy combined with cytotoxic agents has been established as the treatment of choice in the past 10 years. Among chemotherapeutic agents, pegylated liposomal doxorubicin has become the preferred one for patients with HIV-associated Kaposi’s sarcoma in Western countries. The drug in this formulation localizes better to the tumor and has higher efficacy. Skin toxicity, mucositis, and leukopenia/neutropenia are the main side effects. Hepatotoxicity and mild cardiotoxicity are observed less frequently. Pegylated liposomal doxorubicin impacts favorably on quality of life. Although cost effective in Western countries, the drug is less so in developing countries.
Url:
PubMed: 19774206
PubMed Central: 2747337
Affiliations:
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Antiretroviral therapy combined with cytotoxic agents has been established as the treatment of choice in the past 10 years. Among chemotherapeutic agents, pegylated liposomal doxorubicin has become the preferred one for patients with HIV-associated Kaposi’s sarcoma in Western countries. The drug in this formulation localizes better to the tumor and has higher efficacy. Skin toxicity, mucositis, and leukopenia/neutropenia are the main side effects. Hepatotoxicity and mild cardiotoxicity are observed less frequently. Pegylated liposomal doxorubicin impacts favorably on quality of life. Although cost effective in Western countries, the drug is less so in developing countries.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Engels, Ea" uniqKey="Engels E">EA Engels</name></author><author><name sortKey="Biggar, Rj" uniqKey="Biggar R">RJ Biggar</name></author><author><name sortKey="Marshall, Va" uniqKey="Marshall V">VA Marshall</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Chang, Y" uniqKey="Chang Y">Y Chang</name></author><author><name sortKey="Cesarman, E" uniqKey="Cesarman E">E Cesarman</name></author><author><name sortKey="Pessin, Ms" uniqKey="Pessin M">MS Pessin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Moore, Ps" uniqKey="Moore P">PS Moore</name></author><author><name sortKey="Gao, Sj" uniqKey="Gao S">SJ Gao</name></author><author><name sortKey="Dominguez, G" uniqKey="Dominguez G">G 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