Economic evaluation of shortened, bedaquiline-containing treatment regimens for rifampicin-resistant tuberculosis (STREAM stage 2): a within-trial analysis of a randomised controlled trial

Laura Rosu, Jason J. Madan, Ewan Tomeny, Malaisamy Muniyandi, Jasper Nidoi, Mamo Girma, Valentina Vilc, Priyanka Bindroo, Rajdeep Dhandhukiya, Adamu K. Bayissa, Daniel Meressa, Gopalan Narendran, Rajesh Solanki, Anuj K. Bhatnagar, Elena Tudor, Bruce Kirenga, Sarah K. Meredith, Andrew J. Nunn, Gay Bronson, I. D. RusenBertie Squire, Eve Worrall, Saleem Ahmad, Sofia Alexandru, Katharine Bellenger, Tolera G. Bulga, Claire Cook, Valeriu Crudu, Bennet Deborah, Wendy Dodds, Belay A. Gebreegziabher, Ruth L. Goodall, Pritti Gupta, Meera Gurumurthy, Ivor Langley, Joanitah Nalunjogi, Saleem Khan, Saravanan Krishnan, Shravan Kumar, Maia Lesosky, Mariana Macari, Mukesh Makwana, Brendan Murphy, Ramesh P. Murugesan, Vanita Patel, Irina Pirlog, Mary Rauchenberger, Karen Sanders, Ramesh Singh, Sangeetha Subramani

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Abstract

Background

The STREAM stage 2 trial assessed two bedaquiline-containing regimens for rifampicin-resistant tuberculosis: a 9-month all-oral regimen and a 6-month regimen containing an injectable drug for the first 2 months. We did a within-trial economic evaluation of these regimens.

Methods

STREAM stage 2 was an international, phase 3, non-inferiority randomised trial in which participants with rifampicin-resistant tuberculosis were randomly assigned (1:2:2:2) to the 2011 WHO regimen (terminated early), a 9-month injectable-containing regimen (control regimen), a 9-month all-oral regimen with bedaquiline (oral regimen), or a 6-month regimen with bedaquiline and an injectable for the first 2 months (6-month regimen). We prospectively collected direct and indirect costs and health-related quality of life data from trial participants until week 76 of follow-up. Cost-effectiveness of the oral and 6-month regimens versus control was estimated in four countries (oral regimen) and two countries (6-month regimen), using health-related quality of life for cost-utility analysis and trial efficacy for cost-effectiveness analysis. This trial is registered with ISRCTN, ISRCTN18148631.

Findings

300 participants were included in the economic analyses (Ethiopia, 61; India, 142; Moldova, 51; Uganda, 46). In the cost-utility analysis, the oral regimen was not cost-effective in Ethiopia, India, Moldova, and Uganda from either a provider or societal perspective. In Moldova, the oral regimen was dominant from a societal perspective. In the cost-effectiveness analysis, the oral regimen was likely to be cost-effective from a provider perspective at willingness-to-pay thresholds per additional favourable outcome of more than US$4500 in Ethiopia, $1900 in India, $3950 in Moldova, and $7900 in Uganda, and from a societal perspective at thresholds of more than $15 900 in Ethiopia, $3150 in India, and $4350 in Uganda, while in Moldova the oral regimen was dominant. In Ethiopia and India, the 6-month regimen would cost tuberculosis programmes and participants less than the control regimen and was highly likely to be cost-effective in both cost-utility analysis and cost-effectiveness analysis. Reducing the bedaquiline price from $1·81 to $1·00 per tablet made the oral regimen cost-effective in the provider-perspective cost-utility analysis in India and Moldova and dominate over the control regimen in the provider-perspective cost-effectiveness analysis in India.

Interpretation

At current costs, the oral bedaquiline-containing regimen for rifampicin-resistant tuberculosis is unlikely to be cost-effective in many low-income and middle-income countries. The 6-month regimen represents a cost-effective alternative if injectable use for 2 months is acceptable.

Original languageEnglish
Pages (from-to)e265-e277
JournalThe Lancet Global Health
Volume11
Issue number2
Early online date21 Dec 2022
DOIs
Publication statusPublished - 1 Feb 2023

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