Switch from enfuvirtide to raltegravir in virologically suppressed HIV-1 infected patients: effects on level of residual viremia and quality of life.
Switch from enfuvirtide to raltegravir in virologically suppressed HIV-1 infected patients: effects on level of residual viremia and quality of life.
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DOI:
10.1016/j.jcv.2009.09.025
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发表时间:
2009-12
影响因子:
8.8
通讯作者:
Zolopa, Andrew R.
中科院分区:
文献类型:
--
作者:
Grant, Philip M.;Palmer, Sarah;Bendavid, Eran;Talbot, Annie;Slamowitz, Debbie C.;Cain, Pat;Kobayashi, Stacy S.;Balamane, Maya;Zolopa, Andrew R.
Raltegravir is a potential treatment option for virologically suppressed HIV-1 infected patients on enfuvirtide with injection site reactions. To characterize safety and efficacy of an enfuvirtride to raltegravir switch including changes in T cells, quality of life, and residual viremia. In patients with viral load<50 copies/mL and injection site reactions, enfuvirtide was switched to raltegravir without additional changes to the antiretroviral regimen. Virologic failure was defined as a viral load >1000 copies/mL or two consecutive viral load measurements between 50-1000 copies/mL (low-level viremia). Over the 24 week study, we compared changes in T cells, injection site reactions, quality of life, and residual viremia, as measured through the single-copy assay which can detect plasma virus down to a single copy, using paired t-tests. Fourteen patients with a median CD4+ T-cell count of 420 cells/μL were enrolled. After the switch, two patients experienced virologic failure due to confirmed low-level viremia. However, both patients subsequently were resuppressed, one without any changes to his regimen. There was no change in CD4+ T-cell count. Injection site reactions resolved. However, there was little reported change in quality of life. The baseline median level of residual viremia was 6 copies/mL and did not change after the switch to raltegravir. A switch to raltegravir in virologically suppressed patients on enfuvirtide is effective in maintaining immunologic and virologic control at 24 weeks but did not result in a change in residual viremia.
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影响因子:
168.9
作者:
Lennox, Jeffrey L.;Dejesus, Edwin;Sklar, Peter
通讯作者:
Sklar, Peter
影响因子:
158.5
作者:
Riddler, Sharon A.;Haubrich, Richard;Mellors, John W.
通讯作者:
Mellors, John W.
影响因子:
11.8
作者:
Gatell, Jose;Salmon-Ceron, Dominique;Ledesma, Emilio
通讯作者:
Ledesma, Emilio
DOI:
10.1056/nejmoa0803152
发表时间:
2008-10-02
期刊:
The New England journal of medicine
影响因子:
--
作者:
Gulick RM;Lalezari J;Goodrich J;Clumeck N;DeJesus E;Horban A;Nadler J;Clotet B;Karlsson A;Wohlfeiler M;Montana JB;McHale M;Sullivan J;Ridgway C;Felstead S;Dunne MW;van der Ryst E;Mayer H;MOTIVATE Study Teams
通讯作者:
MOTIVATE Study Teams
影响因子:
158.5
作者:
Lalezari, JP;Henry, K;Hersch, J
通讯作者:
Hersch, J