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Initial Antiretroviral Therapy in an Integrase Inhibitor Era: Can We Do Better?
被引:6
|作者:
Kelly, Sean G.
[1
]
Masters, Mary Clare
[2
]
Taiwo, Babafemi O.
[2
]
机构:
[1] Vanderbilt Univ, Med Ctr, Div Infect Dis, A2200 MCN,1161 21st Ave South, Nashville, TN 37232 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Infect Dis, 645 North Michigan Ave,Suite 900, Chicago, IL 60611 USA
关键词:
Integrase stand transfer inhibitors;
Dolutegravir;
Bictegravir;
Dual therapy;
Rapid start;
TENOFOVIR DISOPROXIL FUMARATE;
CO-FORMULATED ELVITEGRAVIR;
STRAND TRANSFER INHIBITOR;
TREATMENT-NAIVE PATIENTS;
VIRUS-INFECTED PATIENTS;
ONCE-DAILY DOLUTEGRAVIR;
HIV-1;
INFECTION;
NON-INFERIORITY;
DOUBLE-BLIND;
REVERSE-TRANSCRIPTASE;
D O I:
10.1016/j.idc.2019.05.003
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
With the second-generation integrase inhibitors (dolutegravir and bictegravir) extending the attributes of earlier integrase inhibitors, three-drug regimens containing integrase inhibitors plus two nucleos(t)ide reverse transcriptase inhibitors are now widely recommended for first-line (initial) treatment of human immunodeficiency virus-1 infection. Led by dolutegravir plus lamivudine, two-drug therapy is emerging as a way to reduce antiretroviral therapy cost and adverse effects without compromising treatment options should virologic failure occur. Initial two-drug therapy has limitations, including the relative incompatibility with the coemerging concept of same-day antiretroviral therapy initiation.
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页码:681 / +
页数:13
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