Projecting the impact of triple CFTR modulator therapy on intravenous antibiotic requirements in cystic fibrosis using patient registry data combined with treatment effects from randomised trials
作者:Ruth H. Keogh, Rebecca Cosgriff, Eleni‐Rosalina Andrinopoulou, K. Brownlee, S.B. Carr, Karla Diaz‐Ordaz, Emily Granger, Nicholas P. Jewell, Alex Lewin, Clémence Leyrat, Daniela K Schlüter, Maarten van Smeden, Rhonda D. Szczesniak, Gary Connett · 发表于:Thorax · 年份:2021 · DOI:10.1136/thoraxjnl-2020-216265 · 被引用次数:26 · 研究领域:Cystic Fibrosis Research Advances、Health Systems, Economic Evaluations, Quality of Life、Respiratory viral infections research
Background Cystic fibrosis (CF) is a life-threatening genetic disease, affecting around 10 500 people in the UK. Precision medicines have been developed to treat specific CF-gene mutations. The newest, elexacaftor/tezacaftor/ivacaftor (ELEX/TEZ/IVA), has been found to be highly effective in randomised controlled trials (RCTs) and became available to a large proportion of UK CF patients in 2020. Understanding the potential health economic impacts of ELEX/TEZ/IVA is vital to planning service provision. Methods We combined observational UK CF Registry data with RCT results to project the impact of ELEX/TEZ/IVA on total days of intravenous (IV) antibiotic treatment at a population level. Registry data from 2015 to 2017 were used to develop prediction models for IV days over a 1-year period using several predictors, and to estimate 1-year population total IV days based on standards of care pre-ELEX/TEZ/IVA. We considered two approaches to imposing the impact of ELEX/TEZ/IVA on projected outcomes using effect estimates from RCTs: approach 1 based on effect estimates on FEV 1 % and approach 2 based on effect estimates on exacerbation rate. Results ELEX/TEZ/IVA is expected to result in significant reductions in population-level requirements for IV antibiotics of 16.1% (~17 800 days) using approach 1 and 43.6% (~39 500 days) using approach 2. The two approaches require different assumptions. Increased understanding of the mechanisms through which ELEX/TEZ/IVA acts on these outcomes wo...