Back to Search Start Over

Comparative Cost-Efficacy Analysis of Darunavir/ritonavir and Other Ritonavir-Boosted Protease Inhibitors for First-Line Treatment of HIV-1 Infection in the United States.

Authors :
Brogan, Anita J.
Mrus, Joseph
Hill, Andrew
Sawyer, Anthony W.
Smets, Erik
Source :
HIV Clinical Trials; May/Jun2010, Vol. 11 Issue 3, p133-144, 12p, 4 Charts, 3 Graphs
Publication Year :
2010

Abstract

Purpose: A comprehensive study comparing the costs and efficacies of darunavir/ritonavir 800/100 mg qd and the other ritonavir-boosted (/r) protease inhibitors (PIs) recommended for treatment-naïve individuals with HIV-1 infection would help health care decision makers identify the value of each boosted PI. Methods: A cost-efficacy model was developed to compare the five recommended boosted PIs, each used with a tenofovir-based nucleotide/nucleoside reverse transcriptase inhibitor backbone. Efficacy was measured by virologic response (ie, HIV-1 ribonucleic acid < 50 copies/mL) at 48 weeks, based on a systematic review and meta-analysis of recent clinical trials. One-year antiretroviral therapy costs and 48-week efficacy values were used to generate the efficiency frontier and cost-efficacy ratios. Results: Darunavir/r was the most efficacious boosted PI, with an incremental cost-efficacy ratio of $27,390 per additional individual with virologic response, compared with fosamprenavir/r. All other regimens were dominated. Darunavir/r combination therapy also had one of the lowest average costs ($26,287) per individual with virologic response, resulting in a maximal number of individuals successfully treated within a fixed budget. The model results were robust in variability and sensitivity analyses. Conclusion: Darunavir/r 800/100 mg qd combination therapy represents a cost-efficacious option for treatment-naïve individuals with HIV-1 infection in the United States. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15284336
Volume :
11
Issue :
3
Database :
Complementary Index
Journal :
HIV Clinical Trials
Publication Type :
Academic Journal
Accession number :
53110444
Full Text :
https://doi.org/10.1310/hct1103-133