HIV Drug Resistance in Adults Receiving Early vs. Delayed Antiretroviral Therapy: HPTN 052

被引:10
|
作者
Palumbo, Philip J. [1 ]
Fogel, Jessica M. [1 ]
Hudelson, Sarah E. [1 ]
Wilson, Ethan A. [2 ]
Hart, Stephen [3 ]
Hovind, Laura [3 ]
Piwowar-Manning, Estelle [1 ]
Wallis, Carole [4 ,5 ]
Papathanasopoulos, Maria A. [6 ]
Morgado, Mariza G. [7 ]
Saravanan, Shanmugam [8 ]
Tripathy, Srikanth [9 ]
Eron, Joseph J. [10 ]
Gallant, Joel E. [11 ]
McCauley, Marybeth [12 ]
Gamble, Theresa [13 ]
Hosseinipour, Mina C. [14 ,15 ]
Kumarasamy, Nagalingeswaran [16 ]
Hakim, James G. [17 ]
Pilotto, Jose H. [18 ,19 ]
Kumwenda, Johnstone [20 ]
Akelo, Victor [21 ]
Godbole, Sheela V. [22 ]
Santos, Breno R. [23 ]
Grinsztejn, Beatriz [24 ]
Panchia, Ravindre [25 ]
Chariyalertsak, Suwat [26 ]
Makhema, Joseph [27 ]
Badal-Faesen, Sharlaa [28 ]
Chen, Ying Q. [2 ]
Cohen, Myron S. [10 ]
Eshleman, Susan H. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[2] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1124 Columbia St, Seattle, WA 98104 USA
[3] Frontier Sci & Technol Res Fdn Inc, Amherst, NY USA
[4] Lancet Labs, Specialty Mol Div, Johannesburg, South Africa
[5] BARC SA, Johannesburg, South Africa
[6] Univ Witwatersrand, Fac Hlth Sci, HIV Pathogenesis Res Unit, Johannesburg, South Africa
[7] Oswaldo Cruz Inst, Lab AIDS & Mol Immunol, Rio De Janeiro, Brazil
[8] YR Gaitonde Ctr AIDS Res & Educ, Madras, Tamil Nadu, India
[9] Natl Inst Res TB, Madras, Tamil Nadu, India
[10] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[11] Southwest CARE Ctr, Dept Specialty Serv, Santa Fe, NM USA
[12] HPTN Leadership & Operat Ctr, FHI 360, Washington, DC USA
[13] HPTN Leadership & Operat Ctr, FHI 360, Durham, NC USA
[14] Univ N Carolina, Div Infect Dis, Chapel Hill, NC USA
[15] UNC Project Malawi, Inst Global Hlth & Infect Dis, Lilongwe, Malawi
[16] YRGCARE Med Ctr, VHS, CART CRS, Madras, Tamil Nadu, India
[17] Univ Zimbabwe, Dept Med, Harare, Zimbabwe
[18] Hosp Geral Nova Iguacu, Rio De Janeiro, Brazil
[19] Lab AIDS & Imunol Mol IOC Fiocruz, Rio De Janeiro, Brazil
[20] Johns Hopkins Project, Coll Med, Blantyre, Malawi
[21] Kenya Med Res Inst KEMRI, CDC, Kisumu, Kenya
[22] Natl AIDS Res Inst ICMR, Dept Epidemiol & Biostat, Pune, Maharashtra, India
[23] Hosp Nossa Senhora Conceicao, Dept Infect Dis, Porto Alegre, RS, Brazil
[24] Inst Nacl Infectol Evandro Chagas INI Fiocruz, Rio De Janeiro, Brazil
[25] Univ Witwatersrand, Soweto HPTN CRS, Perinatal HIV Res Unit, Soweto, South Africa
[26] Chiang Mai Univ, Res Inst Hlth Sci, Chiang Mai, Thailand
[27] Botswana Harvard AIDS Inst Partnership, Gaborone, Botswana
[28] Univ Witwatersrand, Fac Hlth Sci, Sch Clin Med, Dept Internal Med,Clin HIV Res Unit, Johannesburg, South Africa
基金
美国国家卫生研究院;
关键词
HIV; HPTN; 052; early ART; virologic failure; resistance; VIROLOGICAL FAILURE; CELL COUNTS; INITIATION; MUTATIONS; TRIAL; ART; PREVENTION; NAIVE; ACCUMULATION; INFECTION;
D O I
10.1097/QAI.0000000000001623
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: We evaluated HIV drug resistance in adults who received early vs. delayed antiretroviral therapy (ART) in a multinational trial [HIV Prevention Trials Network (HPTN) 052, enrollment 2005-2010]. In HPTN 052, 1763 index participants were randomized to start ART at a CD4 cell count of 350-550 cells/mm(3) (early ART arm) or <250 cells/mm(3) (delayed ART arm). In May 2011, interim study results showed benefit of early ART, and all participants were offered ART regardless of CD4 cell count; the study ended in 2015. Methods: Virologic failure was defined as 2 consecutive viral loads >1000 copies/mL >24 weeks after ART initiation. Drug resistance testing was performed for pretreatment (baseline) and failure samples from participants with virologic failure. Results: HIV genotyping results were obtained for 211/249 participants (128 early ART arm and 83 delayed ART arm) with virologic failure. Drug resistance was detected in 4.7% of participants at baseline; 35.5% had new resistance at failure. In univariate analysis, the frequency of new resistance at failure was lower among participants in the early ART arm (compared with delayed ART arm, P = 0.06; compared with delayed ART arm with ART initiation before May 2011, P = 0.032). In multivariate analysis, higher baseline viral load (P = 0.0008) and ART regimen (efavirenz/lamivudine/zidovudine compared with other regimens, P = 0.024) were independently associated with higher risk of new resistance at failure. Conclusions: In HPTN 052, the frequency of new drug resistance at virologic failure was lower in adults with early ART initiation. The main factor associated with reduced drug resistance with early ART was lower baseline viral load.
引用
收藏
页码:484 / 491
页数:8
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