Paediatric antiretroviral therapy challenges with emerging integrase resistance

Author:

Bamford Alasdair123,Hamzah Lisa4,Turkova Anna13

Affiliation:

1. Great Ormond Street Hospital for Children NHS Foundation Trust

2. UCL Great Ormond Street Institute of Child Health

3. MRC Clinical Trials Unit at UCL

4. St George's University Hospital NHS Trust, London, UK

Abstract

Purpose of review Universal antiretroviral (ART) coverage and virological suppression are fundamental to ending AIDS in children by 2030. Availability of new paediatric dolutegravir (DTG)-based ART formulations is a major breakthrough and will undoubtedly help achieve this goal, but treatment challenges still remain. Recent findings Paediatric formulations remain limited compared to those for adults, especially for young children, those unable to tolerate DTG or with DTG-based first-line ART failure. Tenofovir alafenamide is virologically superior to standard-of-care backbone drugs in second-line, but paediatric formulations are not widely available. The roles of resistance testing and recycling of backbone drugs following first-line ART failure remain to be determined. Results of trials of novel treatment strategies including dual therapy and long-acting agents are awaited. Although numbers are currently small, safe and effective ART options are urgently required for children developing DTG resistance. Summary The antiretroviral treatment gap between adults and children persists. The potential benefits from rollout of new paediatric DTG-based fixed-dose combination ART for first-line treatment are considerable. However, children remain disadvantaged when DTG-based first-line ART fails or cannot be used. Research efforts to address this inequity require prioritisation in order to ensure health outcomes are optimised for all ages in all settings.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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