Drug-resistance or viral load testing required before switch to dolutegravir in Togo

By | December 16, 2019

Dolutegravir-based antiretroviral treatment (ART) in combination with an NRTI backbone will not be effective in Togo, due to high levels of resistance to the NRTI class of drugs, according to a study presented by Professor Mounerou Salou of the Laboratoire Biolim in Togo at the recent 20th International Conference on AIDS and STIs in Africa (ICASA) in Kigali, Rwanda.

Since July 2019, the World Health Organization has recommended dolutegravir-based regimens for as the preferred first-line and second-line treatment for all people living with HIV, including pregnant women and those of childbearing potential. The study examined what potential resistance patterns could exist if all people living with HIV were switched to dolutegravir, as per the WHO recommendations.

As genotypic drug resistance testing is not available in Togo, the study assessed whether a switch to dolutegravir-based treatment in combination with an NRTI backbone of zidovudine (AZT) and lamivudine, or abacavir and lamivudine, would be effective for individuals with virological failure on their current regimen. At present, the standard regimen in Togo is tenofovir disoproxil fumarate (TDF), lamivudine and efavirenz.

Glossary

drug resistance

A drug-resistant HIV strain is one which is less susceptible to the effects of one or more anti-HIV drugs because of an accumulation of HIV mutations in its genotype. Resistance can be the result of a poor adherence to treatment or of transmission of an already resistant virus.

second-line treatment

The second preferred therapy for a particular condition, used after first-line treatment fails or if a person cannot tolerate first-line drugs.

integrase inhibitors (INI, INSTI)

A class of antiretroviral drugs. Integrase strand transfer inhibitors (INSTIs) block integrase (see ‘integrase’). Blocking integrase prevents HIV from replicating.

integrase

HIV enzyme that the virus uses to insert its genetic material into a cell that it has infected.

Between January and September 2018, 1708 people living with HIV on ART received viral load testing, of whom 19% (n=324) had virological failure with viral load of more than 1000 copies/ml. Two hundred of those with virological failure had their plasma samples sequenced to analyse drug resistance mutations.

By drug class, 77% of patients were resistant to both NRTIs and NNRTIs, 2% to NRTIs only, 10% to NNRTIs only and 13% to protease inhibitors. Regarding integrase inhibitors, 12% had minor mutations not inducing resistance to dolutegravir.

These results have implications for potential resistance to NRTIs  in the dolutegravir-based regimen. Genotyping results showed 76% (n=137) of participants had strains with high (n=130) or intermediate (n=7) resistance to lamivudine.  Although patients had not received zidovudine or abacavir during their first-line treatment, 32% (n=58) patients accumulated NRTI mutations that predicted high (n=33) or intermediate (n=25) resistance to zidovudine, 55% (n=99) and 23% (n=41) had high and intermediate resistance to abacavir.

If all patients were switched to a dolutegravir-based lined ART such as TDF and lamivudine and dolutegravir, 51% would be on dolutegravir monotherapy because of drug resistance to lamivudine and TDF.

As genotypic drug resistance testing is not available in Togo, viral load testing is critical to monitor if there is any indication of virological failure due to drug resistance, before switching to a dolutegravir-based regimen which requires these NRTIs.

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“Our data highlight the importance of viral load testing before switch to dolutegravir and for monitoring of patients on suboptimal dolutegravir based regimens, otherwise large-scale switch to dolutegravir could prevent the achievement of the third 90 of UNAIDS objectives and lead to emergence of resistance to integrase inhibitors in Togo,” said Salou.

References

Salou M et al. Dolutegravir Based Regimen in Second Line Treatment in Togo without Resistance Genotyping Tests, Is this Promising? 20th International Conference on AIDS and STIs in Africa (ICASA), Kigali, Rwanda, abstract TUAA0301, 2019.

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