Overview of the effectiveness of triple combination therapy in antiretroviral-naive HIV-1 infected adults

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Abstract
To estimate the effectiveness of triple combination therapy in antiretroviral-naive adults. A systematic overview of results from clinical trials involving triple combination therapy with dual nucleoside reverse transcriptase inhibitors (NRTI) and: a protease inhibitor (PI triple); a non-nucleoside reverse transcriptase inhibitor (NNRTI triple); or a third NRTI (triple NUC). Data from 23 clinical trials involving 31 independent treatment groups, 19 unique antiretroviral regimens, and 3257 enrolled patients were included in this study. Median log10 baseline plasma HIV RNA and CD4 cell count over all trials averaged 4.69 (49 329 copies/ml) and 375 × 106 cells/l, respectively. The overall estimated percentage of patients with plasma HIV RNA ≤ 400 copies/ml at 24 weeks was 64% [95% confidence interval (CI), 60 to 67%]. The percentages of patients with plasma HIV RNA ≤ 50 copies/ml at 48 weeks by drug class were: PI triple, 46% (95% CI, 41 to 52%); NNRTI triple, 51% (95% CI, 43 to 59%); triple NUC, 45% (95% CI, 36 to 54%). The CD4 cell count increase over all trials at 24 and 48 weeks averaged +123 × 106 cells/l (95% CI, 111 × 106 to 135 × 106 cells/l) and +160 × 106 cells/l (95% CI, 146 × 106 to 175 × 106 cells/l), respectively and did not differ between drug classes. In multivariable regression analysis, neither baseline plasma HIV RNA level and CD4 cell count nor treatment regimen predicted plasma HIV RNA ≤ 50 copies/ml at week 48. However, pill count was significantly negatively associated with plasma HIV RNA ≤ 50 copies/ml at week 48 (P = 0.0085). The results suggest that three drug regimens containing two NRTI with a PI, a NNRTI, or a third NRTI may provide comparable activity, and practical issues such as daily pill burden should be considered when choosing a treatment regimen.