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DOI 10.1016/j.cct.2025.107963

Медицинская библиотека · Contemporary clinical trials · 2025

BREATHER Plus clinical trial design: A randomised non-inferiority trial evaluating the efficacy, safety and acceptability of short cycle (five days on, two days off) dolutegravir/tenofovir-based triple antiretroviral therapy (ART) compared to daily ART in virologically suppressed adolescents living with HIV aged 12 to <20 years in sub-Saharan Africa.

Katongole Fredrick, Arumugam Tiyara, Jennings Angus, Mutata Constantine, Ssebunya Patrick, Wamboi Charity, Green Alexandra, Bwakura-Dangarembizi Mutsa, Kityo Cissy, Siika Abraham, Archary Moherndran, Jafta Lungile, Namukwaya Stella, Seeley Janet, Mugerwa Henry, Walker Simon, Apoto Naomi, Thomason Margaret J, Ford Deborah, Pett Sarah L, Kekitiinwa Adeodata R, BREATHER Plus trial team

СтатьяПротокол клинического исследованияПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Novel strategies to improve ART adherence, retention in care and quality of life among adolescents living with HIV (ALHIV) are needed. Short-Cycle Therapy (SCT) with 4/5 sequential days on ART, 2/3 days off ART per week has shown non-inferior virological outcomes and high acceptability, but most data are in adults and are very limited for dolutegravir (DTG)-based SCT.

METHODS

BREATHER Plus is an ongoing 96-week non-inferiority randomised trial evaluating efficacy, safety and acceptability of SCT (5 sequential days on, 2 days off at the weekend) with DTG/tenofovir (TNV)-based triple ART versus continuous (daily) therapy (CT) in ALHIV. Participants are aged 12 to <20 years in Kenya/South Africa/Uganda/Zimbabwe, virologically suppressed (Viral Load (VL) <50copies/mL) for ≥12 months at enrollment, with no prior treatment failure. Randomisation is 1:1 to SCT versus CT. VL monitoring for clinical management is 6-12 monthly aligning with standard-of-care. The primary outcome is confirmed virological rebound ≥50 copies/mL by 96 weeks. The trial employs the Smooth Away From Expected (SAFE) non-inferiority frontier, where the non-inferiority margin depends on the observed event risk in the CT arm. Secondary outcomes include HIV resistance, toxicities, patient-reported outcomes and cost-effectiveness. Enrolment of 470 participants completed in June 2023.

DISCUSSION: BREATHER Plus is the first randomised trial specifically evaluating DTG/TNV-triple based SCT. Rapid roll-out of DTG and a pragmatic approach to VL monitoring mean results will be generalisable to ALHIV across sub-Saharan Africa. If SCT provides non-inferior virological suppression to CT, it may offer choice for ALHIV on how they take their ART.

Для цитирования: Katongole Fredrick, Arumugam Tiyara, Jennings Angus, Mutata Constantine, Ssebunya Patrick, Wamboi Charity, Green Alexandra, Bwakura-Dangarembizi Mutsa, Kityo Cissy, Siika Abraham, Archary Moherndran, Jafta Lungile, Namukwaya Stella, Seeley Janet, Mugerwa Henry, Walker Simon, Apoto Naomi, Thomason Margaret J, Ford Deborah, Pett Sarah L, Kekitiinwa Adeodata R, BREATHER Plus trial team. BREATHER Plus clinical trial design: A randomised non-inferiority trial evaluating the efficacy, safety and acceptability of short cycle (five days on, two days off) dolutegravir/tenofovir-based triple antiretroviral therapy (ART) compared to daily ART in virologically suppressed adolescents living with HIV aged 12 to <20 years in sub-Saharan Africa.. Contemporary clinical trials. 2025. DOI: 10.1016/j.cct.2025.107963.

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