| Literature DB >> 30885693 |
Boris Julg1, Lynda Dee2, Jintanat Ananworanich3, Dan H Barouch4, Katharine Bar5, Marina Caskey6, Donn J Colby7, Liza Dawson8, Krista L Dong9, Karine Dubé10, Joseph Eron11, John Frater12, Rajesh T Gandhi13, Romas Geleziunas14, Philip Goulder15, George J Hanna16, Richard Jefferys17, Rowena Johnston18, Daniel Kuritzkes19, Jonathan Z Li19, Udom Likhitwonnawut20, Jan van Lunzen21, Javier Martinez-Picado22, Veronica Miller23, Luis J Montaner24, Douglas F Nixon25, David Palm26, Giuseppe Pantaleo27, Holly Peay28, Deborah Persaud29, Jessica Salzwedel20, Karl Salzwedel8, Timothy Schacker30, Virginia Sheikh31, Ole S Søgaard32, Serena Spudich33, Kathryn Stephenson4, Jeremy Sugarman34, Jeff Taylor35, Pablo Tebas36, Caroline T Tiemessen37, Randall Tressler8, Carol D Weiss31, Lu Zheng38, Merlin L Robb3, Nelson L Michael3, John W Mellors39, Steven G Deeks40, Bruce D Walker41.
Abstract
Analytical antiretroviral treatment interruption (ATI) is an important feature of HIV research, seeking to achieve sustained viral suppression in the absence of antiretroviral therapy (ART) when the goal is to measure effects of novel therapeutic interventions on time to viral load rebound or altered viral setpoint. Trials with ATIs also intend to determine host, virological, and immunological markers that are predictive of sustained viral control off ART. Although ATI is increasingly incorporated into proof-of-concept trials, no consensus has been reached on strategies to maximise its utility and minimise its risks. In addition, differences in ATI trial designs hinder the ability to compare efficacy and safety of interventions across trials. Therefore, we held a meeting of stakeholders from many interest groups, including scientists, clinicians, ethicists, social scientists, regulators, people living with HIV, and advocacy groups, to discuss the main challenges concerning ATI studies and to formulate recommendations with an emphasis on strategies for risk mitigation and monitoring, ART resumption criteria, and ethical considerations. In this Review, we present the major points of discussion and consensus views achieved with the goal of informing the conduct of ATIs to maximise the knowledge gained and minimise the risk to participants in clinical HIV research.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30885693 PMCID: PMC6688772 DOI: 10.1016/S2352-3018(19)30052-9
Source DB: PubMed Journal: Lancet HIV ISSN: 2352-3018 Impact factor: 12.767