Durability of HIV-1 viral suppression over 3.3 years with multi-drug antiretroviral therapy in previously drug-naive individuals

被引:51
作者
Phillips, AN
Miller, V
Sabin, C
Lepri, AC
Klauke, S
Bickel, M
Doerr, HW
Hill, A
Staszewski, S
机构
[1] UCL, Dept Primary Care & Populat Sci, Royal Free & Univ Coll Med Sch, London NW3 2PF, England
[2] UCL, Royal Free Ctr HIV Med, Royal Free & Univ Coll Med Sch, London NW3 2PF, England
[3] Univ Frankfurt, D-6000 Frankfurt, Germany
[4] Roche Prod Ltd, Welwyn Garden City AL7 3AY, Herts, England
[5] Univ Frankfurt, Inst Med Virol, D-6000 Frankfurt, Germany
关键词
HAART; viral suppression; long term follow-up; viral load; viral rebound;
D O I
10.1097/00002030-200112070-00005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Relatively little is known about the long-term durability of viral suppression in individuals initially achieving a viral load of less than 50 copies/ml within 24 weeks of starting antiretroviral therapy, nor the extent to which therapy interruption accounts for the loss of suppression. Methods: We intensely followed all 336 anti retroviral-naive patients attending the Goethe Universitat Clinic who began multi-drug combination regimens and in whom a viral load of less than 50 copies/ml was achieved within 24 weeks, in order to assess the risk of viral load rebound. Inspection of case notes allowed the distinction of viral rebound according to whether there was an associated complete interruption of therapy. Results: A total of 61 patients experienced viral rebound during 543.1 person-years of follow-up, giving a 25.3% risk of rebound by 3.3 years from first achieving viral suppression. However, for 47 of the patients with viral rebound there was an associated documented complete interruption of antiretroviral therapy, mostly as a result of co-morbidities, leaving 14 who appear to represent a failure of the virological efficacy of therapy (viral breakthrough; 5.2% risk by 3.3 years). The risk of viral breakthrough declined with the increased duration of suppression (P = 0.01). Conclusion: The intrinsic virological effectiveness of multi-drug antiretroviral therapy in previously drug-naive individuals appears to be such that viral suppression, once achieved, can be maintained for several years in patients not interrupting therapy. The major challenge is to develop regimens that can be taken consistently and safely for such long periods of time. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:2379 / 2384
页数:6
相关论文
共 33 条
[1]  
Clayton D., 1993, STAT MODELS EPIDEMIO
[2]  
*DEP HHS, 2001, GUID US ANT AG HIV I
[3]   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
[4]   Impact of new antiretroviral combination therapies in HIV infected patients in Switzerland: prospective multicentre study [J].
Egger, M ;
Hirschel, B ;
Francioli, P ;
Sudre, P ;
Wirz, M ;
Flepp, M ;
Rickenbach, M ;
Malinverni, R ;
Vernazza, P ;
Battegay, M ;
Bernasconi, E ;
Burgisser, P ;
Erb, P ;
Fierz, W ;
Grob, P ;
Gruninger, U ;
Jeannerod, L ;
Ledergerber, B ;
Luthy, R ;
Matter, L ;
Opravil, M ;
Paccaud, F ;
Perrin, L ;
Pichler, W ;
Piffaretti, GC ;
Rutschmann, O ;
Zanetti, G .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7117) :1194-1199
[5]   Discontinuation of prophylaxis against Mycobacterium avium complex disease in HIV-infected patients who have a response to antiretroviral therapy. [J].
El-Sadr, WM ;
Burman, WJ ;
Grant, LB ;
Matts, JP ;
Hafner, R ;
Crane, L ;
Zeh, D ;
Gallagher, B ;
Mannheimer, SB ;
Martinez, A ;
Gordin, F .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (15) :1085-1092
[6]   Latent infection of CD4+ T cells provides a mechanism for lifelong persistence of HIV-1, even in patients on effective combination therapy [J].
Finzi, D ;
Blankson, J ;
Siliciano, JD ;
Margolick, JB ;
Chadwick, K ;
Pierson, T ;
Smith, K ;
Lisziewicz, J ;
Lori, F ;
Flexner, C ;
Quinn, TC ;
Chaisson, RE ;
Rosenberg, E ;
Walker, B ;
Gange, S ;
Gallant, J ;
Siliciano, RF .
NATURE MEDICINE, 1999, 5 (05) :512-517
[7]  
FISCHL M, 2001, 8 C RETR OPP INF CHI
[8]   Discontinuation of primary prophylaxis against Pneumocystis carinii pneumonia in HIV-1-infected adults treated with combination antiretroviral therapy [J].
Furrer, H ;
Egger, M ;
Opravil, M ;
Bernasconi, E ;
Hirschel, B ;
Battegay, M ;
Telenti, A ;
Vernazza, PL ;
Rickenbach, M ;
Flepp, M ;
Malinverni, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (17) :1301-1306
[9]   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
[10]  
GRUEB G, 2001, 8 C RETR OPP INF CHI