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.
引用
收藏
页码:681 / +
页数:13
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