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POSTER PRESENTATION Open Access Treatment of HIV-2 infection with ritonavir/ lopinavir: results at 60 months. A single-center study of 9 patients Philippe Genet * , Tahar Touahri, Laurence Courdavault, Frédérique Plassart, Juliette Gerbe From 16 th International Symposium on HIV and Emerging Infectious Diseases Marseille, France. 24-26 March 2010 Background In vitro and in vivo data have suggested that ritonavir/ lopinavir is one of the most potent protease inhibitor against HIV-2 infection. Nevertheless, only few clinical reports have been published. So, it seemed to us impor- tant to report our clinical experience in 9 patients. Methods We searched in our database patients with HIV-2 who have been treated with ritonavir/lopinavir. 9 patients (4 women and 5 men) were identified. Clinical and biologi- cal evolution was analyzed. Results At the time of initiation of lopinavir, median age was 54 (37-66). Median duration of HIV infection was 41,6 months (6-101). Previous median duration of treatment was 29 months (4-51). No patient was naïve of treat- ment. The median previous number of regimens received was 2 (1-2). 5/9 patients were naïve of protease inhibitors. Initial median CD4 cells were 150 (68-478). Viral load (VL) was under the limit of detection in 6 cases. Reasons for switching to lopinavir were toxicity or intolerance (n = 2), absence of efficacy on VL (n = 3) or inadequacy of previous treatment (n = 4). In all cases, lopinavir was given in association of 2 NRTIs. After a median follow-up of 60 months (18-84), no severe side effect was observed. VL under the limits of detection was obtained for all patients except for one patient with a very poor compliance. In this later case, after switching lopinavir to raltegravir, VL remained undetectable. CD4 increased in all cases. The median gain of CD4 from baseline was + 234 (+50 - +472). Discussion Because of the very low frequency of the disease in wes- tern countries, data on the treatment of HIV-2 infection are uncommon. For these reasons, treatment of HIV-2 patients remains difficult. So, reports on therapeutic options are very important. Even with a modest number of patients, we confirmed the excellent long-term effi- ciency of lopinavir for the treatment of HIV-2 patients. Published: 11 May 2010 doi:10.1186/1742-4690-7-S1-P47 Cite this article as: Genet et al.: Treatment of HIV-2 infection with ritonavir/lopinavir: results at 60 months. A single-center study of 9 patients. Retrovirology 2010 7(Suppl 1):P47. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit * Correspondence: [email protected] CH Victor Dupouy, Argenteuil, France Genet et al. Retrovirology 2010, 7(Suppl 1):P47 http://www.retrovirology.com/content/7/S1/P47 © 2010 Genet et al; licensee BioMed Central Ltd.

Treatment of HIV-2 infection with ritonavir/lopinavir: results at 60 months. A single-center study of 9 patients

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POSTER PRESENTATION Open Access

Treatment of HIV-2 infection with ritonavir/lopinavir: results at 60 months. A single-centerstudy of 9 patientsPhilippe Genet*, Tahar Touahri, Laurence Courdavault, Frédérique Plassart, Juliette Gerbe

From 16th International Symposium on HIV and Emerging Infectious DiseasesMarseille, France. 24-26 March 2010

BackgroundIn vitro and in vivo data have suggested that ritonavir/lopinavir is one of the most potent protease inhibitoragainst HIV-2 infection. Nevertheless, only few clinicalreports have been published. So, it seemed to us impor-tant to report our clinical experience in 9 patients.

MethodsWe searched in our database patients with HIV-2 whohave been treated with ritonavir/lopinavir. 9 patients (4women and 5 men) were identified. Clinical and biologi-cal evolution was analyzed.

ResultsAt the time of initiation of lopinavir, median age was 54(37-66). Median duration of HIV infection was 41,6months (6-101). Previous median duration of treatmentwas 29 months (4-51). No patient was naïve of treat-ment. The median previous number of regimensreceived was 2 (1-2). 5/9 patients were naïve of proteaseinhibitors. Initial median CD4 cells were 150 (68-478).Viral load (VL) was under the limit of detection in 6cases. Reasons for switching to lopinavir were toxicity orintolerance (n = 2), absence of efficacy on VL (n = 3) orinadequacy of previous treatment (n = 4). In all cases,lopinavir was given in association of 2 NRTIs.After a median follow-up of 60 months (18-84), no

severe side effect was observed. VL under the limits ofdetection was obtained for all patients except for onepatient with a very poor compliance. In this later case,after switching lopinavir to raltegravir, VL remained

undetectable. CD4 increased in all cases. The mediangain of CD4 from baseline was + 234 (+50 - +472).

DiscussionBecause of the very low frequency of the disease in wes-tern countries, data on the treatment of HIV-2 infectionare uncommon. For these reasons, treatment of HIV-2patients remains difficult. So, reports on therapeuticoptions are very important. Even with a modest numberof patients, we confirmed the excellent long-term effi-ciency of lopinavir for the treatment of HIV-2 patients.

Published: 11 May 2010

doi:10.1186/1742-4690-7-S1-P47Cite this article as: Genet et al.: Treatment of HIV-2 infection withritonavir/lopinavir: results at 60 months. A single-center study of 9patients. Retrovirology 2010 7(Suppl 1):P47.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submit

* Correspondence: [email protected] Victor Dupouy, Argenteuil, France

Genet et al. Retrovirology 2010, 7(Suppl 1):P47http://www.retrovirology.com/content/7/S1/P47

© 2010 Genet et al; licensee BioMed Central Ltd.