Real-world data on the efficacy and safety of tezacaftor-ivacaftor in adults living with cystic fibrosis homozygous for F508del and heterozygous for F508del and a residual function mutation

ABSTRACT

Background

To examine safety and efficacy of tezacaftor-ivacaftor (TEZ/IVA) in a real-life setting in adults living with cystic fibrosis.

Methods

A multicentre retrospective observational study, including adults living with cystic fibrosis (pwCF) eligible for TEZ/IVA, with assessments at baseline, 3 months (visit_3mo) and 6 months (visit_6mo) after start of treatment. Outcomes included change in FEV₁, LCI, FeNO, CFQ-R, estimated number of annual acute exacerbations, BMI, dosage of pancreatic enzyme replacement therapy (PERT) and airway microbiology. We also assessed safety.

Results

Forty-eight adult pwCF (mean (±SD) age 33 (±12) years; mean FEV₁ 65 (±19) %P) were included. Three subgroups were identified: pwCF F/F CFTR modulator-naive (n = 28; 58%), pwCF F/F previously treated with lumacaftor-ivacaftor (n = 11; 23%) and pwCF F/RF (n = 9; 19%). Adverse events were described in 3 pwCF (6%) during the 6-month observation period (in one leading to treatment interruption). At visit_3mo, FEV₁ had improved in all subgroups. In the entire group, mean FEV₁ had increased from 66 (±2.9) %P to 72 (±2.9) %P (p < 0.0001). Similarly, LCI improved by approximately one unit at visit_3mo (p = 0.02). At visit_6mo mean annual acute exacerbation rate decreased significantly (p = 0.02). Only in the CFQ-R social functioning domain score, a significant improvement was observed at visit_6mo (p < 0.01).

Conclusions

We showed that TEZ/IVA is safe, well tolerated and effective in terms of improvement of lung function, ventilation inhomogeneity, health-related social functioning, and reduction of estimated annual acute exacerbation rate, in adult pwCF F/F and F/RF. Results in this real-life study reflect those observed in RCTs.

KEYWORDS:

• Cystic fibrosis
• tezacaftor-ivacaftor
• CFTR modulator
• real-world data

Disclosure statement

Competing interests: Stefanie Vincken, Eef Vanderhelst and Christiane Knoop served as (sub-)investigator for Vertex Pharmaceuticals. Eef Vanderhelst and Christiane Knoop also served in advisory boards for Vertex Pharmaceuticals. All other authors: no competing interests to declare.

Additional information

Funding

this research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.