Patients with cystic fibrosis (CF) who take the drug, Ivacaftor, appear to have fewer respiratory infections over time than those not taking the drug, according to new research findings published online in the Annuals of the American Thoracic Society.
The hereditary disorder, Cystic fibrosis, is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Ivacaftor (Kalydeco®) is prescribed to patients whose CF is caused by a “gating” mutation. This group of mutations, which are responsible for about 4 percent of all CF cases, prevents chloride from moving in and out of cells. By restoring the gate’s function, ivacaftor has been shown to improve lung function and quality of life.
In the published study, \”Ivacaftor Is Associated with Reduced Lung Infection by Key Cystic Fibrosis Pathogens: A Cohort Study Using National Registry Data,\” researchers in the United Kingdom (UK) say that ivacaftor may also reduce some of the most common lung infections in patients with CF, including P. aeruginosa. If this is proven, they say, it may mean that some patients taking ivacaftor can take fewer antibiotics long term while still remaining clinically stable.
Common Lung Infections Reduced by Taking Ivacaftor
“People with CF notice improvement in lung function and quality of life soon after they start taking ivacaftor, but they still have to live with a considerable treatment burden from all the other medications they take,” said lead author Freddy Frost, BMBS, a cystic fibrosis physician at Liverpool Heart & Chest Hospital in a July 29 statement detailing the study’s findings. “At present, we simply don’t know whether it’s safe to stop some of those other treatments. The fact we have seen reduced infections in this study suggests there may be some people who can safely discontinue medications targeted towards those infections,” he says.
The researchers, using data gleaned from a CF registry in the U.K, compared CF patients (age six and older) who took ivacaftor with those CF patients who did not take the drug over a three-year period. They found that ivacaftor was associated with a 32 percent reduction in the number of people infected with P. aeruginosa and a 15 percent reduction in Staphylococcus aureus.
These reductions resulted from both increased clearance of the infection in those already infected and in reduced acquisition in those not infected.
According to the authors, people starting ivacaftor combined with other drugs that correct defects in the CF gene from an early age, the possibility of preventing these infections is particularly exciting. “If these drugs are taken before chronic infection starts, the risk of developing infection in the future may be reduced considerably,” says Dr. Frost.
The researchers say Ivacaftor was also associated with reduced Aspergillus spp. infections. The drug did not appear to reduce Burkholderia cepacia complex infections, they say.
Dr. Frost notes that this study adds to the increasing evidence of the long-term benefits of ivacaftor. “However,” he cautioned, “randomized, controlled trials will be needed to know if it is safe to reduce the overall treatment burden of CF by decreasing antibiotic use in patients taking ivacaftor or other drugs that target defects in the CF gene.”