Abstract
Introduction
In a previous interim 24-week virological safety analysis of the PROTEST study [1], initiation of Maraviroc (MVC) plus 2 nucleoside reverse-transcriptase inhibitors (NRTIs) in aviremic subjects based on genotypic tropism testing of proviral HIV-1 DNA was associated with low rates of virological failure. Here we present the final 48-week analysis of the study.
Methods
PROTEST was a phase 4, prospective, single-arm clinical trial (ID: NCT01378910) carried on in 24 HIV care centres in Spain. Maraviroc-naïve HIV-1-positive adults with HIV-1 RNA (VL) <50 c/mL on stable ART during the previous 6 months, requiring an ART change due to toxicity, with no antiretroviral resistance to the ART started, and R5 HIV by proviral DNA genotypic tropism testing (defined as a G2P FPR >10% in a singleton), initiated MVC with 2 NRTIs and were followed for 48 weeks. Virological failure was defined as two consecutive VL>50 c/mL. Recent adherence was calculated as: (# pills taken/# pills prescribed during the previous week)*100.
Results
Tropism results were available from 141/175 (80.6%) subjects screened: 87/141 (60%) were R5 and 74/87 (85%) were finally included in the study. Their median age was 48 years, 16% were women, 31% were MSM, 36% had CDC category C at study entry, 62% were HCV+ and 10% were HBV+. Median CD4+ counts were 616 cells/mm3 at screening, and median nadir CD4+ counts were 143 cells/mm3. Previous ART included PIs in 46 (62%) subjects, NNRTIs in 27 (36%) and integrase inhibitors (INIs) in 1 (2%). The main reasons for treatment change were dyslipidemia (42%), gastrointestinal symptoms (22%), and liver toxicity (15%). MVC was given alongside TDF/FTC in 40 (54%) subjects, ABC/3TC in 30 (40%), AZT/3TC in 2 (3%) and ABC/TDF in 2 (3%). Sixty-two (84%) subjects maintained VL<50 c/mL through week 48, whereas 12 (16%) discontinued treatment: two (3%) withdrew informed consent, one (1%) had a R5→X4 shift in HIV tropism between the screening and baseline visits, one (1%) was lost to follow-up, one (1%) developed an ART-related adverse event (rash), two (3%) died due to non-study-related causes (1 myocardial infarction at week 0 and 1 lung cancer at week 36), and five (7%) developed protocol-defined virological failure, although two of them regained VL<50 c/mL with the same MVC regimen (Table 1).
Conclusions
Initiation of MVC plus 2 NRTIs in aviremic subjects based on genotypic tropism testing of proviral HIV-1 DNA is associated with low rates of virological failure up to one year.
Table 1.
| Subject | ART | Week of VF | HIV-1 VL at VF (c/mL) | Plasma tropism at VF (FPR,%) | Recent adherence at VF (%) | Resistance mutations at VF (IAS-USA 2013) | ART after VF | Regained VL <50 c/mL |
|---|---|---|---|---|---|---|---|---|
| 1 | MVC+TDF/FTC | 4 | 300 | X4 (0.1) | 100 | NA | DRV/r+ETV | Yes |
| 2 | MVC+TDF/FTC | 12 | 14,102 | X4 (1.3) | 100 | RT: 41L, 67N, 184V, 215Y PR: 36I, 63P | TDF/FTC+ETV | Yes |
| 3 | MVC+ABC/3TC | 12 | 67 | R5 (86.8) | 100 | RT: 90I, 184I PR: 64V | TDF+DRV/r+EFV | Yes |
| 4 | MVC+TDF/FTC | 12 | 59 | NA | 100 | NA | Continued with MVC+TDF/FTC | Yes |
| 5 | MVC+TDF/FTC | 36 | 90 | R5 (79.7) | 100 | NA | Continued with MVC+TDF/FTC | Yes |
Reference
- 1.Federico Garcìa, Eva Poveda, Maria Ångels Ribas, María Jesús Pérez-Elías, Onofre J. Martínez-Madrid, Jordi Navarro, et al. Genotypic tropism testing of proviral DNA to guide maraviroc initiation in aviremic subjects; 21st Conference on Retroviruses and Opportunistic Infections 2014; Boston, US: 2014. Feb 3–6, (Abstract#: 607) [Google Scholar]