Two-drug regimens for HIV treatment

被引:17
|
作者
Gibas, Kevin M. [1 ]
Kelly, Sean G. [1 ]
Arribas, Jose R. [2 ,3 ,4 ]
Cahn, Pedro [5 ]
Orkin, Chloe [6 ]
Daar, Eric S. [7 ]
Sax, Paul E. [8 ,9 ]
Taiwo, Babafemi O. [10 ]
机构
[1] Vanderbilt Univ, Med Ctr, Div Infect Dis, Nashville, TN USA
[2] La Paz Univ Hosp, Hosp La Paz Inst Hlth Res, Infect Dis Unit, Madrid, Spain
[3] Univ Autonoma Madrid, Sch Med, Madrid, Spain
[4] Ctr Invest Biomed Red Enfermedades Infecciosas, Madrid, Spain
[5] Fdn Huesped, Buenos Aires, DF, Argentina
[6] Queen Mary Univ London, Dept Immunobiol, London, England
[7] Harbor Univ Calif, Lundquist Inst, Tonrence, CA USA
[8] Brigham & Womens Hosp, Div Infect Dis, Boston, MA USA
[9] Harvard Univ, Harvard Med Sch, Boston, MA USA
[10] Northwestern Univ, Feinberg Sch Med, Div Infect Dis, Chicago, IL 60611 USA
来源
LANCET HIV | 2022年 / 9卷 / 12期
基金
美国医疗保健研究与质量局;
关键词
DOLUTEGRAVIR PLUS LAMIVUDINE; HUMAN-IMMUNODEFICIENCY-VIRUS; ANTIRETROVIRAL-NAIVE ADULTS; REVERSE-TRANSCRIPTASE INHIBITORS; TENOFOVIR DISOPROXIL FUMARATE; VIROLOGICALLY STABLE PATIENTS; LONG-ACTING CABOTEGRAVIR; BUDGET IMPACT ANALYSIS; NON-INFERIORITY; OPEN-LABEL;
D O I
10.1016/S2352-3018(22)00249-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Combination therapy with three antiretroviral agents has been integral to successful HIV-1 treatment since 1996. Although the efficacy, adverse effects, and toxicities of contemporary three-drug regimens have improved, even the newest therapies have potential adverse effects. The use of two-drug regimens is one way to reduce lifetime exposure to antiretroviral drugs while maintaining the benefits of viral suppression. Multiple large, randomised trials have shown the virological non-inferiority of certain two-drug regimens versus three-drug comparators, including adverse effect differences that reflect known profiles of the antiretroviral drugs in the respective regimens. Two-drug combinations are now recommended in treatment guidelines and include the first long-acting antiretroviral regimen for the treatment of HIV-1. Recommended two-drug regimens differ in their risks for, and factors associated with, virological failure and emergent resistance. The tolerability, safety, metabolic profiles, and drug interactions of two-drug regimens also vary by the constituent drugs. No current two-drug regimen is recommended for people with chronic hepatitis B virus as none include tenofovir. Two-drug regimens have increased options for individualised care.
引用
收藏
页码:E868 / E883
页数:16
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