Abstract

The aim of this proof-of-concept study is to test feasibility and efficacy of NVP plus Lamivudine (3TC) as novel simplified HIV maintenance dual therapy (DT) strategy. Patients under combined antiretroviral treatment (cART) with fully suppressed HIV plasma viral load (pVL) >24 months-whereof >6 months on an NVP- containing regimen-were switched to oral NVP plus 3TC for 24 weeks. Patients could then decide whether to continue DT or return to the previous cART. HIV pVL was monitored monthly until week 144. The primary outcome was confirmed viral failure (RNA >100 copies/ml). Low-level detection of HIV-RNA in plasma was compared in each patient with pre-study viral load measurements. Twenty patients were included, switched to DT and all completed week 24. One patient decided thereafter to discontinue study participation for personal reasons. After a total of 144 observation weeks, none of the patients failed. The frequency of low- level HIV-RNA detection was not different from the period before randomization. Our findings are surprising but given the nature of a proof-of-concept study, the results do not support the use of this dual regimen. However, as this dual HIV maintenance strategy was feasible and effective, over a period of 144 weeks, we suggest NVP plus 3TC warrants further evaluation as potential maintenance option in patients tolerating nevirapine. A properly sized multicentre non-inferiority trial is ongoing to further evaluate the value of this DT maintenance strategy.

Highlights

  • Today, combination antiretroviral therapy is recommended for all patients with HIV infection [1]

  • Our findings are surprising but given the nature of a proof-of-concept study, the results do not support the use of this dual regimen

  • The combination of several antiretroviral compounds is essential at the start of treatment, as high viral replication can allow rapid development of resistance

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Summary

Introduction

Combination antiretroviral therapy (cART) is recommended for all patients with HIV infection [1]. Lifelong cART demand from the patient a long breath by daily regular intake of medication and is associated with potential long-term adverse events and high cost. The combination of several antiretroviral compounds is essential at the start of treatment, as high viral replication can allow rapid development of resistance. Afterwards, viral replication is completely suppressed and a simplified treatment with two antiretroviral compounds (dual therapy–DT) or even one substance (monotherapy) may hypothetically control viral replication on the long run. The underlying hypothesis of a simplified treatment with two antiretroviral compounds (dual therapy–DT) or even one substance (monotherapy) is, that low viral replication is associated with a reduced risk of viral escape and may control viral replication on the long run. Some MT demonstrated evidence for a decreased antiretroviral activity in the central nervous system [3, 4]

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