# Ivacaftor Therapy in CF Patients: Single Center Experience

**Authors:** Pritish Mondal, Amber Loyson, Jorge Lascano, Satyanarayan Hegde

PMC · DOI: 10.1155/2014/947923 · Advances in Medicine · 2014-10-22

## TL;DR

This paper shares a single center's experience with Ivacaftor therapy in cystic fibrosis patients, showing significant improvements in lung function and health.

## Contribution

The study demonstrates that Ivacaftor can significantly improve lung function in patients with established lung disease, unlike previous findings.

## Key findings

- Patients with established lung disease showed a 35% improvement in mean FEV1 after Ivacaftor therapy.
- Ivacaftor led to subjective and objective health improvements in both pediatric and adult cystic fibrosis patients.
- The study highlights the potential of Ivacaftor in patients with diminished lung function, contrasting with prior studies.

## Abstract

Ivacaftor is the first novel cystic fibrosis pharmaceutical that acts at the molecular level to potentiate cystic fibrosis transmembrane conductance regulator (CFTR) function and was first approved for clinical use in 2012. We are sharing our single center experience of five patients: four from pediatric age group and one adult patient. All patients had both subjective and objective improvements in their health. Despite established lung disease, our patients had significant improvement in both their FEV1 (forced expiratory volume in 1 second) and FEF25–75 and BMI (body mass index). Larger studies demonstrated only 6.7% improvement in mean FEV1 after starting Ivacaftor therapy but their patient population had normal lung function to begin with. In contrast our case series demonstrates that, in patients with established lung disease and diminished lung function, Ivacaftor can be expected to result in much higher recovery in lung function. Mean FEV1 improved by 35% in our case series. Ivacaftor is extremely expensive, costing $300,000 per patient per year requiring lifelong therapy, hence requiring prior authorizations from most third-party payers in the USA. The knowledge shared from our experience will be useful for other clinicians to petition healthcare policymakers on behalf of their patients.

## Linked entities

- **Proteins:** CFTR (CF transmembrane conductance regulator)
- **Chemicals:** Ivacaftor (PubChem CID 16220172)
- **Diseases:** cystic fibrosis (MONDO:0009061)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** MRSA (MESH:D013203), respiratory (MESH:D012131), obese (MESH:D009765), diffuse (MESH:D008228), lung damage (MESH:D008171), diabetes (MESH:D003920), flow obstruction (MESH:D054318), bacterial infection (MESH:D001424), autosomal recessive disease (MESH:D030342), CF (MESH:D003550), bronchiectasis (MESH:D001987)
- **Chemicals:** Ivacaftor (MESH:C545203), chloride (MESH:D002712), vitamin D (MESH:D014807), Methicillin (MESH:D008712)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** del F508, 2789 + 5G > A, G551D

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4590953/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC4590953/full.md

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Source: https://tomesphere.com/paper/PMC4590953