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Dolutegravir brings faster viral suppression in late pregnancy

Among 60 women presenting to routine antenatal clinics in Kampala, Uganda and Cape Town, South Africa with undiagnosed HIV in late pregnancy, viral load suppression was faster in those starting dolutegravir (DTG) – compared to efavirenz (EFV)-based antiretroviral therapy (ART). Dr Saye Khoo, on behalf of the DolPHIN-1 study group, presented data at the 22nd International AIDS Conference (AIDS 2018) held in Amsterdam recently.

Findings from this randomised controlled pilot study by researchers at the Desmond Tutu HIV Foundation, Cape Town, Infectious Diseases Institute-Kampala, University of Liverpool, University of Cape Town and Imperial College London provide a potential means to reduce mother-to-child transmission at birth and during breastfeeding for women starting ART in late pregnancy.

Approximately 1.5m women living with HIV become pregnant each year, 90% of whom live in resource-poor settings and who continue to present late (third trimester) in their pregnancy with untreated HIV. In South Africa around one in five pregnant women living with HIV start ART late. Starting ART in the third trimester is associated with failure to achieve viral suppression (< 50 copies/ml) by delivery, which is critical for prevention of mother-to-child transmission. Starting late is associated with a sevenfold increased risk of mother-to-child transmission, as well as a doubling of infant death in the first year. Recommended first-line ART (EFV-based) takes a median of 84 days to reach viral suppression compared to 28 days for DTG-based ART.

The primary endpoint in this study was the pharmacokinetics (drug absorption, distribution, and excretion) of DTG in women and breastfed infants two weeks after delivery, while secondary endpoints included viral suppression at delivery as well as the safety and tolerability of DTG in pregnant women and their infants.

A scheduled interim analysis after the first 16 (eight on DTG) delivered, presented at CROI 2018, (poster #807) found DTG to be safe and confirmed that DTG exposure in the third trimester did not warrant a dose increase. The analysis also confirmed that mothers who start ART in late pregnancy are a vulnerable group who may have a higher rate of treatment failure. In compliance with national guidelines (starting women on ART on the day diagnosed), standard of care EFV + two nucleoside reverse transcriptase inhibitors (NRTIs) began on referral with randomisation to continue standard of care or switch to DTG + two NRTIs a median of three (IQR:1-8) days later.

In Uganda, the NRTIs comprised tenofovir and lamivudine and in South Africa, tenofovir and emtricitabine. DTG and EFV dosage was 50mg and 600mg daily, respectively. Viral load was monitored at every visit. Intensive maternal pharmacokinetics sampling was done (0.5,1, 2, 3, 4, 6, 8 and 24 hours) after two weeks on DTG and two weeks after delivery, with paired sampling between maternal plasma and cord blood, breast milk and infant plasma. All infants were breastfed. No significant differences before starting ART were seen between the DTG (n = 29) and the EFV (n = 31) arms in maternal age, length of pregnancy (median 31 weeks), weight, obstetric history, viral load (over 90% > 1000 copies/ml) or CD4 cell count (median 394 cells/mm3).

In just over a third of the women (9/28) DTG exposures in the third trimester were low with concentration levels (Ctrough) at or below the minimum effective concentration of 324ng/ml.

Significant infant exposure, possibly continuing through breastfeeding, was due to DTG transfer across the placenta (122%) and in breast milk (3%) together with delayed drug elimination.

At two weeks postpartum viral suppression (< 50 copies/ml) with DTG was significantly higher compared to EFV, 69% (20) and 39% (12), p = 0.02. Median time to viral suppression was approximately halved with DTG compared to EFV.

In the DTG arm, one mother had undetectable DTG concentrations with no viral load response, while another with DTG concentrations < 64 ng/ml had virological rebound. There were no HIV transmissions. The regimens were well tolerated – 95% (57) had normal healthy births with comparable infant outcomes. The median duration of pregnancy at birth was 38 weeks with a median infant weight of three kilogrammes.

Limitations include the small sample size, relatively short follow-up and prior EFV use in all mothers (subsequently randomised to DTG) starting ART, although the safety of DTG and EFV was comparable. This pilot study showed a significantly greater proportion of mothers starting ART late in pregnancy achieved viral suppression with DTG-based, compared to EFV-based, regimens. DolPHIN-2, comprising 250 women, a randomised comparison of starting ART in the third trimester with DTG compared to EFV, will further evaluate these findings.

Background: ART initiation in the 3rd trimester of pregnancy is associated with failure to achieve viral suppression (VS) by delivery and increased transmission of HIV. We randomised 60 treatment naïve pregnant women at 28-36w gestation in Uganda and South Africa 1:1 to receive EFV or DTG+2NRTIs. The primary endpoint was pharmacokinetics (PK) of DTG in women and breastfed infants; secondary endpoints included VS.
Methods: To comply with national guidelines, EFV+2NRTI was initiated on referral, with subjects randomized to DTG switched within 7 days. Viral load (VL) was collected at every visit; intensive maternal PK sampling (0-24h) was performed at 14 days on DTG, and 2 weeks post-partum, with paired sampling between maternal plasma and cord blood, breastmilk and infant plasma. All infants were exclusively breastfed.
Results: There was no significant pre-ART differences between DTG (n=29) and EFV (n=31) arms in maternal age, gestation at treatment initiation (30.8w), weight, obstetric history, VL (log 4 copies) and CD4 count (394 cells/mm3). Third trimester DTG exposures were low with Ctrough at or below target (MEC 324ng/mL) in 9/28 (32%) mothers. DTG transfer across the placenta (122%) and in breast milk (3%) coupled with delayed elimination resulted in significant infant exposures potentially persisting during breast-feeding. Both regimens were well-tolerated. A total of 10 SAEs were reported in 5 mothers and 3 infants, with no significant differences between arms.
Superior VS was observed with DTG (Table 1) at the 2w post-partum visit (P=0.005). However, VL>1000 copies/mL near delivery was still observed with both DTG (3.7%) and EFV (7.4%). No HIV transmissions were observed
Conclusions: HIV RNA suppression < 50 copies/mL was more rapid with DTG (despite low DTG exposures when started in the third trimester) which may translate to improved PMTCT for ART initiation in late pregnancy. The impact of significant infant DTG exposures related to intrauterine transfer, continued breastfeeding and delayed elimination is being evaluated in the DolPHIN-2 study.

C Orrell, K Kintu, JA Coombs, A Amara, L Myer, J Kaboggoza, B Simmons, L Else, C Heiberg, C Waitt, S Walimbwa, EM Hodel, A Hill, S Khoo, M Lamorde, DolPHIN-1 Study Group

[link url=""]Aidsmap material[/link]
[link url=""]AIDS 2018 abstract 13144[/link]

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