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Review
. 2012 Jan;13(1):65-79.
doi: 10.1517/14656566.2012.642865.

Combination nucleoside/nucleotide reverse transcriptase inhibitors for treatment of HIV infection

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Review

Combination nucleoside/nucleotide reverse transcriptase inhibitors for treatment of HIV infection

Maxwell O Akanbi et al. Expert Opin Pharmacother. 2012 Jan.

Erratum in

  • Erratum.
    [No authors listed] [No authors listed] Expert Opin Pharmacother. 2015 May;16(7):1119. doi: 10.1517/14656566.2015.1039789. Expert Opin Pharmacother. 2015. PMID: 25887247 No abstract available.

Abstract

Introduction: The combination of two nucleoside/nucleotide reverse transcriptase inhibitors (N(t)RTIs) and a third agent from another antiretroviral class is currently recommended for initial antiretroviral therapy. In general, N(t)RTIs remain relevant in subsequent regimens. There are currently six nucleoside reverse transcriptase inhibitors and one nucleotide reverse transcriptase inhibitor drug entities available, and several formulations that include two or more N(t)RTIs in a fixed-dose combination. These entities have heterogeneous pharmacological and clinical properties. Accordingly, toxicity, pill burden, dosing frequency, potential drug-drug interaction, preexisting antiretroviral drug resistance and comorbid conditions should be considered when constructing a regimen. This approach is critical in order to optimize virologic efficacy and clinical outcomes.

Areas covered: This article reviews N(t)RTI combinations used in the treatment of HIV-infected adults. The pharmacological properties of each N(t)RTI, and the clinical trials that have influenced treatment guidelines are discussed.

Expert opinion: It is likely that N(t)RTIs will continue to dominate the global landscape of HIV treatment and prevention, despite emerging interest in N(t)RTI-free combination therapy. Clinical domains where only few alternatives to N(t)RTIs exist include treatment of HIV/HBV coinfection and HIV-2. There is a need for novel N(t)RTIs with enhanced safety and resistance profiles compared with current N(t)RTIs.

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References

    1. Sterne JAC, Hernán MA, Ledergerber B, et al. Long-term effectiveness of potent antiretroviral therapy in preventing AIDS and death: a prospective cohort study. The Lancet. 2005;366:378–384. - PubMed
    1. Gazzard BG on behalf of the BTGWG. British HIV Association guidelines for the treatment of HIV-1-infected adults with antiretroviral therapy 2008. HIV Medicine. 2008;9:563–608. - PubMed
    1. Hammer SM, Eron JJ, Reiss P, et al. Antiretroviral Treatment of Adult HIV Infection. JAMA: The Journal of the American Medical Association. 2008;300:555–570. - PubMed
    1. World Health Organization. Geneva: World Health Organization; 2010. Antiretroviral therapy for HIV infection in adults and adolescents: Recommendations for a public health approach: 2010 revision. - PubMed
    1. Piliero PJ. Pharmacokinetic properties of nucleoside/nucleotide reverse transcriptase inhibitors. J Acquir Immune Defic Syndr. 2004;37(Suppl 1):S2–S12. (This article provides an overview of N(t)RTI pharmacokinetics)

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