Mechanisms of early virologic failure in antiretroviral-naive patients starting protease inhibitor-containing regimens:: The APROVIR study

被引:25
作者
Masquelier, B
Peytavin, G
Leport, C
Droz, C
Duran, S
Verdon, R
Besnier, JM
Chêne, G
Raffi, F
Brun-Vézinet, F
机构
[1] CHU Bordeaux, Hop Pellegrin, Virol Lab, F-33076 Bordeaux, France
[2] Univ Bordeaux 2, INSERM, U330, F-33076 Bordeaux, France
[3] Hop Bichat Claude Bernard, Pharmacol Lab, F-75877 Paris, France
[4] Hop Bichat Claude Bernard, Serv Malad Infect & Trop, F-75877 Paris 18, France
[5] Hop Bichat Claude Bernard, Virol Lab, F-75877 Paris 18, France
[6] INSERM, U379, F-13258 Marseille, France
[7] CHU Cote Nacre, Serv Malad Infect, Caen, France
[8] Hop Bretonneau, Serv Malad Infect, Tours, France
[9] Hotel Dieu Nantes, Serv Malad Infect & Trop, Nantes, France
关键词
D O I
10.1086/344358
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The virologic and pharmacologic mechanisms of virologic failure (VF) were studied in 243 antiretroviral-naive patients starting first-line protease inhibitor (PI)-containing therapy (nelfinavir in 66% and indinavir in 19%). Among the 220 patients with follow-up data, VF occurred in 35 (16%) during the first year of follow-up. A higher baseline virus load and poorer adherence to therapy were associated with VF. At the time of VF, key PI-resistance mutations were detected in 11 (48%) of 23 patients who started on nelfinavir but were absent in 6 patients with indinavir treatment failure. PI plasma levels were more often below the range of active concentrations in VF with wild-type viruses (74%) than in VF with PI-resistant viruses (25%; P = .02). The mechanisms of early VF and of selection of PI-resistant viruses differed by type of PI and were dependent on PI plasma levels.
引用
收藏
页码:1503 / 1507
页数:5
相关论文
共 15 条
[1]   Correlation between human immunodeficiency virus genotypic resistance and virologic response in patients receiving nelfinavir monotherapy or nelfinavir with lamivudine and zidovudine [J].
Atkinson, B ;
Isaacson, J ;
Knowles, M ;
Mazabel, E ;
Patick, AK .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (02) :420-427
[2]  
BERNSTEIN B, 2001, 8 C RETR OPP INF CHI, P178
[3]  
Burger DM, 1998, ANTIVIR THER, V3, P215
[4]  
Carrieri P, 2001, J ACQ IMMUN DEF SYND, V28, P232, DOI 10.1097/00042560-200111010-00005
[5]   Mechanisms of virologic failure in previously untreated HIV-infected patients from a trial of induction-maintenance therapy [J].
Descamps, D ;
Flandre, P ;
Calvez, V ;
Peytavin, G ;
Meiffredy, V ;
Collin, G ;
Delaugerre, C ;
Robert-Delmas, S ;
Bazin, B ;
Aboulker, JP ;
Pialoux, G ;
Raffi, F ;
Brun-Vézinet, F .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (02) :205-211
[6]  
DUVAL X, 2000, 38 INF DIS SOC AM M
[7]   Factors associated with clinical and virological failure in patients receiving a triple therapy including a protease inhibitor [J].
Grabar, S ;
Pradier, C ;
Le Corfec, E ;
Lancar, R ;
Allavena, C ;
Bentata, M ;
Berlureau, P ;
Dupont, C ;
Fabbro-Peray, P ;
Poizot-Martin, I ;
Costagliola, D .
AIDS, 2000, 14 (02) :141-149
[8]   Drug susceptibility in HIV infection after viral rebound in patients receiving indinavir-containing regimens [J].
Havlir, DV ;
Hellmann, NS ;
Petropoulos, CJ ;
Whitcomb, JM ;
Collier, AC ;
Hirsch, MS ;
Tebas, P ;
Sommadossi, JP ;
Richman, DD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (02) :229-234
[9]   Antiretroviral drug resistance testing in adult HIV-1 infection -: Recommendations of an International AIDS Society-USA panel [J].
Hirsch, MS ;
Brun-Vézinet, F ;
D'Aquila, RT ;
Hammer, SM ;
Johnson, VA ;
Kuritzkes, DR ;
Loveday, C ;
Mellors, JW ;
Clotet, B ;
Conway, B ;
Demeter, LM ;
Vella, S ;
Jacobsen, DM ;
Richman, DD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (18) :2417-2426
[10]   Determination of nelfinavir, a potent HIV protease inhibitor, and its active metabolite M8 in human plasma by high-performance liquid chromatography with photodiode-array detection [J].
Lamotte, C ;
Peytavin, G ;
Farinotti, R .
JOURNAL OF CHROMATOGRAPHY B, 1999, 735 (02) :159-170