Factors Influencing the Emergence of Resistance to Indinavir: Role of Virologic, Immunologic, and Pharmacologic Variables
Author(s) -
George L. Drusano,
John A. Bilello,
Daniel S. Stein,
Michael L. Nessly,
Anne R. Meibohm,
Emilio A. Emini,
Paul Deutsch,
Jon H. Condra,
J Chodakewitz,
Daniel Holder
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/515631
Subject(s) - indinavir , zidovudine , lamivudine , combination therapy , regimen , medicine , protease inhibitor (pharmacology) , drug resistance , viral load , immunology , chemotherapy , lentivirus , virology , pharmacotherapy , oncology , human immunodeficiency virus (hiv) , sida , virus , viral disease , biology , antiretroviral therapy , microbiology and biotechnology , hepatitis b virus
A major problem with the use of human immunodeficiency virus type 1 (HIV-1) protease inhibitors as monotherapy has been an unacceptably high rate of emergence of resistance. To examine possible influences on the time to emergence of resistance, 24-week data were examined from five studies in which indinavir had been administered as monotherapy or as a component of combination therapy. Monotherapy data indicated a correlation between the level of HIV-1 RNA achieved and the risk of emergence of resistance: the lower the level, the lower the risk. When combination and monotherapy regimens were compared, the group receiving indinavir + lamivudine + zidovudine had a significantly lower risk of resistance, even after adjusting for the minimum HIV-1 RNA level achieved. The findings indicate that if at all possible, HIV-1-infected patients should receive combination chemotherapy to minimize the emergence of resistance to the protease inhibitor portion of the regimen. The goal of therapy should be to decrease the HIV-1 RNA load to a less-than-detectable level.
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