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Review
. 2024 Jun;11(6):e419-e426.
doi: 10.1016/S2352-3018(24)00061-4. Epub 2024 Apr 30.

Two-drug regimens for the treatment of HIV in Africa

Affiliations
Review

Two-drug regimens for the treatment of HIV in Africa

Ivan Mambule et al. Lancet HIV. 2024 Jun.

Abstract

Two-drug regimens for the treatment of HIV are increasingly available. The oral regimen of dolutegravir plus lamivudine is recommended as a preferred option in multiple national guidelines but is not currently included in WHO HIV treatment guidelines nor widely used in Africa. Long-acting injectable cabotegravir and rilpivirine is being rolled out in the USA, Europe, and Australia but its use in sub-Saharan Africa is currently restricted to clinical trials. Given the increasing life expectancy, rising prevalence of non-communicable diseases, and resulting polypharmacy among people living with HIV, there are potential advantages to the use of two-drug regimens, particularly in African women, adolescents, and older adults. This Viewpoint reviews existing evidence and highlights the risks, benefits, and key knowledge gaps for the use of two-drug regimens in settings using the public health approach in Africa. We suggest that a two-drug regimen of dolutegravir and lamivudine can be safely used as a switch option for virologically suppressed individuals in settings using the public health approach once chronic hepatitis B has been excluded. Individuals with HIV who are switched to two-drug regimens should receive a full course of hepatitis B vaccinations. More efficacy data is needed to support dolutegravir plus lamivudine combination in the test and treat approach, and long-acting cabotegravir and rilpivirine in the public health system in sub-Saharan Africa.

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Conflict of interest statement

Declarationsof interests FVC has received research funding from Janssen, ViiV, and Gilead. Additionally, FVC is a DSMB member of same-day treatment for a TB trial in South Africa. LAO has received research funding from ViiV, Gilead, and Janssen, and consulting fees from ViiV and GSK. ER has received research funding from Janssen. SS has received research funding from Janssen and ViiV. IM, CN, EALO, DSL, NO, and FVC have received salary support through research funding awarded by Janssen. All other authors declare no competing interests.

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