HIV-1 genotypic resistance patterns predict response to saquinavir-ritonavir therapy in patients in whom previous protease inhibitor therapy had failed

Background: Tests for resistance to HIV drugs are available for clinical us e; however, their predictive Value has not been fully assessed. Objectives: To determine HIV-1 genotypic predictors of a virologic response to saquinavir-ritonavir therapy in patients in whom at least one previous protease inhibitor-containing regimen had failed and to compare the predict ive value of baseline genotype with that of standard clinical evaluation. Design: Retrospective clinical cohort study. Setting: University-based HIV clinic. Patients: 54 H.IV-1-infected adults treated with saquinavir-ritonavir who h ad experienced virologic failure while receiving a protease inhibitor-conta ining regimen for at least 3 months. Measurements: HIV-1 reverse transcriptase and protease gene sequences, CD4 cell counts, clinical characteristics, detailed antiretroviral treatment hi story, and plasma HIV-1 RNA levels at baseline and at three follow-up time points (median, 4, 12, and 26 weeks). Virologic failure was defined as a pl asma HIV RNA level greater than 1000 copies/mL. Results: In 22 patients (41%), a plasma HIV-1 RNA level less than 500 copie s/mL was achieved by week 12; in 15 patients (28%), this response was maint ained through week 26. Clinical characteristics predicting a poorer respons e included a diagnosis of AIDS, Tower CD4 cell count, and higher plasma HIV RNA level (P < 0.03). Number of previous nucleoside reverse transcriptase inhibitors, previous protease inhibitor therapy, and duration of previous p rotease inhibitor therapy were predictors of poorer response (P < 0.01). Mu ltivariate regression models revealed that protease mutations present at th e initiation of saquinavir-ritonavir therapy were the strongest predictors of virologic response. A model of clinical features explained up to 45% of the variation in virologic outcomes by week 12, whereas the explained varia nce was 71% when genotypic predictors were included. Conclusions: In patients in whom protease inhibitor-containing antiretrovir al therapy fails, HIV-1 genotype is predictive of virologic response to sub sequent therapy. This predictive capacity adds to that of standard clinical evaluation.