Dolutegravir superior to standard-of-care in young children: results from the ODYSSEY trial
1 August 2021. Related: Conference reports, Paediatric care, Paediatric Workshop 13 virtual 2021.
Polly Clayden, HIV i-Base
Dolutegravir (DTG)-based ART was superior to standard-of-care in children weighing 3 to 14 kg, starting first- or second-line treatment.
These 96 week results from the younger cohort of the ODYSSEY trial were presented at the 13th International Workshop on HIV Paediatrics 2021. [1]
ODYSSEY, a multi-country randomised trial, showed superior efficacy for DTG plus two NRTIs vs standard-of-care in 707 children and adolescents weighing 14 kg or more (median age 12 years), starting first- or second-line ART. These results were presented earlier this year at CROI 2021. [2]
Late breaking results, shown at the workshop, were for an additional cohort of 85 younger children weighing less than 14 kg, who completed 96 weeks follow-up on 28 June 2021.
The children were randomised: 42 to DTG and 43 to standard-of-care (Uganda 43, Zimbabwe 22, South Africa 20).
Their median age was 1.4 years (IQR 0.6 to 2.0); 23 were 3 to <6 kg, 40 were 6 to <10 kg and 22 were 10 to <14 kg. Seventy two children started first-line and 13 started second-line ART; 74% in the standard-of-care arm received boosted lopinavir.
Median follow-up was 120 (IQR 97 to 132) weeks; 5 (6%) children were lost to follow-up.
The investigators performed three analyses to estimate the difference in the probability of clinical/virological failure by 96 weeks between DTG-based ART and standard-of-care in children weighing <14 kg:
- Stand-alone analysis, using data only from children <14 kg.
- Pooled analysis, assuming the treatment difference is identical in children <14 kg and >14 kg, and combining the two data sets (they allocated a weight of approximately 90% to data from children >14 kg).
- Bayesian analysis, using information from the 707 children as a prior distribution and clinical opinion todetermine how much weight is given to the that (based on interviews with paediatricians they assigned a weight of 78% to data from the older children).
There were 11 children in the DTG arm with virological or clinical failure by 96 weeks (26%) vs 21 (49%) in standard-of-care; 8 (19%) vs 16 (37%) failures were virological. Of 6 deaths, 2 (5%) were in the DTG and 4 (9%) in the standard-of-care arms.
The investigators found that there was less probability of failing in the DTG vs standard-of-care arm, p=0.05.
For the difference in proportion with virological or clinical failure by 96 weeks <14 kg, the Bayesian analysis gave an 11% difference in favour of DTG: -0.106 (95% CI -0.192 to -0.020). The other analyses also favoured DTG vs standard-of-care: stand-alone -0.196 (95% CI -0.379 to -0.005) and pooled -0.094 (95% CI -0.146 to -0.038). Test of heterogeneity of treatment effect between >14kg and <14kg: p=0.24.
At 96 weeks, 76% of children in the DTG arm had viral load <50 copies/mL compared with 50% in standard-of-care, p=0.02. The corresponding proportions with cut-off <400 copies/mL were 91% vs. 71%, p=0.03.
At 48 weeks, these proportions were 44% and 49% for <50 copies/mL, p=0.69. And 74% vs 69% for <400 copies/mL, p=0.69.
There were a total of 34 serious adverse events: 15 (11 children) in the DTG arm vs 19 (11 children) in standard of care, p=0.92. This included the 2 vs 4 deaths. And 36 (19 children) had grade 3 and above adverse events in DTG vs 34 (21 children) in standard-of-care, p=0.79. There were 2 ART-modifying events in the standard-of-care arm: 1 raised liver enzymes and 1 vomiting.
At 96 weeks there was a significant difference in mean change in total cholesterol (mg/dL) from baseline in children <14 kg also favoring DTG: -26 (95% CI -42 to -9), p=0.003.
Presenting author, Pauline Amuge from Uganda, noted that these results support WHO guidelines and roll-out of DTG-based regimens for younger children starting first- or second-line ART and she added: “procurement of dispersible DTG for children <20 kg should be expedited”.
comment
These results provide good evidence for rapid global rollout of DTG for children aged four weeks and above using the new dispersible 10 mg tablets. [3]
Following this ODYSSEY late breaker, WHO released a statement. [4] This applauded the results and emphasised the grim reality that children living with HIV still continue to be left behind by the global HIV response.
In 2020, only 54% of the 1.7 million children living with HIV received ART compared to 74% of adults. Among WHO focus countries, only 40% of children (or 74% of children receiving ART) achieved viral suppression.
WHO has recommended DTG-based ART for all infants and children since 2018 and provided dosing recommendations for those over four weeks old and weighing more than 3 kg in July 2020.
New WHO 2021 consolidated guidelines on HIV [5] and the newly released policy brief on transitioning to the 2021 optimal formulary for antiretroviral drugs for children [6] give further guidance on how to transition to DTG-containing regimens as well as how to best dose it when co-treatment for TB is needed.
Two generic formulations of DTG 10 mg dispersible tablets have been tentatively approved by the US FDA. [3] The cost for children in low- and middle-income countries where these are available is $4.50 for a 90-tablet bottle.
References
- Amuge P et al Dolutegravir-based ART is superior to standard of care in young children living with HIV. 13th International Workshop on HIV Paediatrics 2021(virtual workshop).16–17 July 2021. Late breaker oral abstract 124.
- Clayden P. Dolutegravir superior to standard of care in children and adolescents: results from the ODYSSEY trial. 1 June 2021.
https://i-base.info/htb/40697 - Clayden P. New formulation of dolutegravir will make modern ART available for babies and young children at less than $120 a year. 9 December 2020.
https://i-base.info/htb/39465 - WHO statement. New findings from the ODYSSEY trial confirm superiority of dolutegravir-based ART in young children. 16 July 2021.
https://www.who.int/news/item/16-07-2021-new-findings-from-the-odyssey-trial-confirm-superiority-of-dolutegravir-based-art-in-young-children. - WHO. Consolidated guidelines on HIV prevention, testing, treatment, service delivery and monitoring: recommendations for a public health approach. 16 July 2021.
https://www.who.int/publications/i/item/9789240031593 - WHO. Transitioning to the 2021 optimal formulary for antiretroviral drugs for children: implementation considerations.16 July 2021.
https://www.who.int/publications/i/item/9789240031371
This report was first posted on 17 July 2021.