Resistance analyses in highly experienced patients failing raltegravir, etravirine and darunavir/ritonavir regimen

被引:15
作者
Charpentier, Charlotte [1 ]
Roquebert, Benedicte [1 ]
Colin, Celine [2 ]
Taburet, Anne-Marie [3 ]
Fagard, Catherine [2 ,4 ]
Katlama, Christine
Molina, Jean-Michel [5 ]
Jacomet, Christine [6 ]
Brun-Vezinet, Francoise [1 ]
Chene, Genevieve [2 ]
Yazdanpanah, Yazdan [7 ]
Descamps, Diane [1 ]
机构
[1] Univ Paris Diderot, Hop Bichat Claude Bernard, AP HP, Lab Virol,EA 4409, F-75018 Paris, France
[2] INSERM, U897, Bordeaux, France
[3] Hop Bicetre, AP HP, Pharmacol Lab, Le Kremlin Bicetre, France
[4] UPMC, Hop La Pitie Salpetriere, AP HP, INSERM,Serv Malad Infect,U943, Paris, France
[5] Univ Paris Diderot, Hop St Louis, AP HP, Serv Malad Infect, F-75018 Paris, France
[6] Hop Clermont Ferrand, Clermont Ferrand, France
[7] Hop Tourcoing, Serv Malad Infect & Trop, Tourcoing, France
关键词
darunavir; etravirine; HIV-1; raltegravir; resistance; VIROLOGICAL FAILURE; DOUBLE-BLIND; HIV-1-INFECTED PATIENTS; TMC125; ETRAVIRINE; EFFICACY; SAFETY; DARUNAVIR; THERAPY;
D O I
10.1097/QAD.0b013e32833ed2a7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: ANRS 139 TRIO trial was a phase II noncomparative trial that evaluated in highly experienced patients, a combination of raltegravir, etravirine and darunavir boosted with ritonavir. We analyzed emergence of resistant viruses at the time of virological failure and investigated the impact of baseline integrase polymorphisms on virological failure occurrence. Methods: Bulk sequencing of protease, reverse transcriptase and integrase genes was performed for 103 patients at baseline and 14 patients at the time of virological failure. Additionally, integrase clonal analyses were performed at baseline and at virological failure in patients with successful integrase gene amplification. Impact of baseline integrase polymorphisms on virological failure occurrence was analyzed using Fisher exact and Wilcoxon tests. Results: In the 14 failing patients median viral load at virological failure was 90 copies/ml (interquartile range = 60-783). Emergence of darunavir and etravirine resistance mutations was observed at virological failure in only one and three patients, respectively. Raltegravir resistance mutations were found neither at baseline nor at the time of virologic failure. Integrase clonal analyses showed neither the presence nor the selection of minority variants carrying raltegravir resistance mutations at baseline or at virological failure. No impact of baseline integrase polymorphisms was observed on virological failure either at week 24 or at week 48. Conclusion: Virological failure occurred in a small proportion of patients with low viral load. No raltegravir resistance mutations were observed using bulk sequencing or clonal analyses, and darunavir and etravirine resistance-associated mutations were detected in only one and three patients, respectively at virological failure. No impact of baseline integrase polymorphism was observed on virological failure occurrence. (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:2651 / 2656
页数:6
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