The long‐term impact and value of curative therapy for HIV: a modelling analysis

Author:

Guzauskas Gregory F.12ORCID,Hallett Timothy B.3

Affiliation:

1. The Comparative Health Outcomes, Policy, and Economics Institute Department of Pharmacy University of Washington Seattle Washington USA

2. HCD Economics Daresbury UK

3. MRC Centre for Global Infectious Disease Analysis Imperial College London London UK

Abstract

AbstractIntroductionCurative therapies (CTx) to achieve durable remission of HIV disease without the need for antiretroviral therapy (ART) are currently being explored. Our objective was to model the long‐term health and cost outcomes of HIV in various countries, the impact of future CTx on those outcomes and the country‐specific value‐based prices (VBPs) of CTx.MethodsWe developed a decision‐analytic model to estimate the future health economic impacts of a hypothetical CTx for HIV in countries with pre‐existing access to ART (CTx+ART), compared to ART alone. We modelled populations in seven low‐and‐middle‐income countries and five high‐income countries, accounting for localized ART and other HIV‐related costs, and calibrating variables for HIV epidemiology and ART uptake to reproduce historical HIV outcomes before projecting future outcomes to year 2100. Health was quantified using disability‐adjusted life‐years (DALYs). Base case, pessimistic and optimistic scenarios were modelled for CTx+ART and ART alone. Based on long‐term outcomes and each country's estimated health opportunity cost, we calculated the country‐specific VBP of CTx.ResultsThe introduction of a hypothetical CTx lowered HIV prevalence and prevented future infections over time, which increased life‐years, reduced the number of individuals on ART, reduced AIDS‐related deaths, and ultimately led to fewer DALYs versus ART‐alone. Our base case estimates for the VBP of CTx ranged from $5400 (Kenya) up to $812,300 (United States). Within each country, the VBP was driven to be greater primarily by lower ART coverage, lower HIV incidence and prevalence, and higher CTx cure probability. The VBP estimates were found to be greater in countries where HIV prevalence was higher, ART coverage was lower and the health opportunity cost was greater.ConclusionsOur results quantify the VBP for future curative CTx that may apply in different countries and under different circumstances. With greater CTx cure probability, durability and scale up, CTx commands a higher VBP, while improvements in ART coverage may mitigate its value. Our framework can be utilized for estimating this cost given a wide range of scenarios related to the attributes of a given CTx as well as various parameters of the HIV epidemic within a given country.

Funder

Bill and Melinda Gates Foundation

Publisher

Wiley

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health

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