Acquired immunodeficiency syndrome-related Kaposi's sarcoma regression after highly active antiretroviral therapy: biologic correlates of clinical outcome.

Abstract

BACKGROUND:

Kaposi's sarcoma (KS) is the most common cancer seen in subjects with acquired immunodeficiency syndrome (AIDS). KS etiology and pathogenesis are still ill defined, and no definite improvement in survival has been obtained with current chemotherapeutic regimens. This open prospective study was aimed at evaluating the clinical response of AIDS-related KS to highly active antiretroviral therapy (HAART), a combination of protease and reverse transcriptase inhibitors, as well as the relationship between clinical response, human immunodeficiency virus type 1 (HIV-1) burden, and antibody titer against human herpesvirus 8 (HHV8) proteins.

PATIENTS AND METHODS:

Fourteen KS patients were studied; 12 were in the poor-risk group. At given intervals, the patients underwent clinical examination, and their CD4(+) cell counts, plasma HIV-1 RNA levels, and antibody titers to lytic-phase ORF65 and latent-phase HHV8 proteins were determined.

RESULTS:

When last seen, the overall clinical response rate was 86% (median follow-up, 22 months); 10 complete and two partial responses were achieved, and two patients showed disease progression. All patients with complete or partial response showed a consistent decrease in HIV-1 RNA levels, with a corresponding increase in CD4(+) cell counts; HIV-1 RNA levels in the two progressors remained persistently high, despite a change in HAART. HHV8 ORF65 antibody titers were generally higher in patients with extensive skin or mucosal/visceral involvement versus patients with limited disease; no differences in latent-phase HHV8 antibody titers were observed in relation to tumor burden.

CONCLUSION:

The findings indicate that antiretroviral therapy with protease inhibitors is effective for AIDS-related KS; the clinical response was correlated with a decrease in plasma HIV-1 RNA levels and an increase in CD4(+) lymphocytes, whereas antibody levels to the lytic-phase HHV8 protein were influenced by the extent of tumor involvement.

• Authors: A M Cattelan, M L Calabrò, P Gasperini, S M Aversa, M Zanchetta, F Meneghetti, A De Rossi, L Chieco-Bianchi
• Journal: Journal of the National Cancer Institute. Monographs (J Natl Cancer Inst Monogr) Issue 28 Pg. 44-9 ( 2001) ISSN: 1052-6773 [Print] United States
• PMID: 11158206 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-HIV Agents
• Antibodies, Viral
• Antiviral Agents
• HIV Protease Inhibitors
• RNA, Viral
• Reverse Transcriptase Inhibitors

Topics

• Acquired Immunodeficiency Syndrome (complications, drug therapy)
• Adult
• Anti-HIV Agents (therapeutic use)
• Antibodies, Viral (blood)
• Antiretroviral Therapy, Highly Active
• Antiviral Agents (therapeutic use)
• CD4 Lymphocyte Count
• Disease Progression
• Drug Evaluation
• Follow-Up Studies
• HIV Protease Inhibitors (therapeutic use)
• HIV-1 (isolation & purification)
• Herpesvirus 8, Human (immunology)
• Humans
• Male
• Middle Aged
• Mucous Membrane (pathology)
• Prospective Studies
• RNA, Viral (blood)
• Remission Induction
• Reverse Transcriptase Inhibitors (therapeutic use)
• Sarcoma, Kaposi (blood, drug therapy, etiology, pathology, virology)
• Skin Neoplasms (blood, drug therapy, etiology, pathology, virology)
• Soft Tissue Neoplasms (blood, drug therapy, etiology, pathology, virology)
• Treatment Outcome
• Viral Load
• Viremia (drug therapy, virology)
• Viscera (pathology)