scholarly journals 178: Long-term impact of ivacaftor on health outcomes and mortality in people with cystic fibrosis in the U.S. CF Foundation Patient Registry (CFFPR)

2021 ◽  
Vol 20 ◽  
pp. S88
Author(s):  
C. Merlo ◽  
M. DerSarkissian ◽  
C. Nguyen ◽  
Y. Gu ◽  
A. Muthukumar ◽  
...  
Author(s):  
Eric Van Ganse ◽  
Alexandra Dima ◽  
Laurent Laforest ◽  
Flore Jacoud ◽  
Sandrine Herbage ◽  
...  

2019 ◽  
Vol 13 ◽  
pp. 175346661882018 ◽  
Author(s):  
Jaime L. Rubin ◽  
Lasair O’Callaghan ◽  
Christopher Pelligra ◽  
Michael W. Konstan ◽  
Alexandra Ward ◽  
...  

Background: Lumacaftor/ivacaftor combination therapy is efficacious and generally safe for patients with cystic fibrosis (CF) homozygous for the F508del-CF transmembrane conductance regulator (CFTR) mutation. However, long-term survival benefits of lumacaftor/ivacaftor (LUM/IVA) cannot yet be quantified. Simulation models can provide predictions about long-term health outcomes. In this study, we aimed to project long-term health outcomes of LUM/IVA plus standard care (SC) in patients with CF homozygous for F508del-CFTR. Methods: This modeling study was an individual patient simulation in US patients aged ⩾6 years with CF, homozygous for F508del-CFTR. The primary outcome was projected survival among (a) a cohort of patients who ever initiated LUM/IVA, accounting for treatment discontinuations, and (b) a cohort of patients who remain on continuous LUM/IVA. Patient characteristics and model parameters were derived from clinical trials: VX14-809-109, VX13-809-011B, TRAFFIC/TRANSPORT, and PROGRESS; published literature; and the US CF Foundation Patient Registry. Results: Lumacaftor/ivacaftor + SC is expected to increase median survival by 6.1 years versus SC alone, accounting for treatment discontinuations. The incremental median predicted survival versus SC assuming initiation of LUM/IVA at ages 6, 12, 18, and 25 years was 17.7, 12.6, 8.0, and 3.8 years, respectively. Assuming lifetime treatment with LUM/IVA, incremental median survival was predicted to be 7.8 years longer in the LUM/IVA + SC cohort. Initiating LUM/IVA at ages 6, 12, 18, and 25 years and assuming lifetime treatment resulted in incremental median predicted survival of 23.4, 18.2, 11.0, and 4.8 years, respectively. Conclusions: Lumacaftor/ivacaftor is projected to increase survival for patients with CF. Initiation at an early age and treatment persistence result in further increments in projected survival.


2020 ◽  
Vol 19 ◽  
pp. S27
Author(s):  
T. Dwyer ◽  
R. Dentice ◽  
J. Marouvo ◽  
P. Bye ◽  
J. Alison

2008 ◽  
Vol 93 (4) ◽  
pp. 357-358 ◽  
Author(s):  
F Festini ◽  
G Taccetti ◽  
V Galici ◽  
S Campana ◽  
G Mergni ◽  
...  

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