Non-White Patients Miss Out On Life-Saving Cystic Fibrosis Drugs Due to Genetic Test Limitations
Poor Representation of Non-White CF Patients in Drug Trials Has Effectively Prohibited Them From Receiving the Most Effective Treatments, Says Study
There are many new drugs to treat cystic fibrosis, but non-white patients are far less likely to receive the latest precision medicines, accord to a new study. These drugs were approved by the U.S. Food and Drug Administration (FDA) for people with specific mutations, but non-white patients are more likely to carry different CF mutations. Because these other mutations aren’t included in genetic tests to qualify for the drugs, doctors cannot prescribe these new treatments for non-white patients, and insurance carriers won’t cover the cost.
The findings were published Feb. 1, 2021, in Pediatric Pulmonology, by Meghan McGarry, MD, MS, assistant professor of pediatrics at UC San Francisco, and co-author Susanna A. McColley, MD, from Ann & Robert H. Lurie Children’s Hospital of Chicago and professor of pediatrics Northwestern University Feinberg School of Medicine.
“The new drugs are remarkable – they take people from almost needing a lung transplant to leaving the hospital within days,” said McGarry. “The problem is that these drugs are only approved for people with specific mutations, and everyone else gets left out. That is going to increase preexisting disparities.”
“We have known for many years that people with cystic fibrosis who are from racial or ethnic minority groups have more severe disease and earlier mortality than White people with this disease,” said McColley. “This reflects findings across populations that are related to systemic and structural inequities. While there is a rationale for developing treatments to help the greatest number of people, the reduced availability of these remarkably effective therapies increases this disparity. It's more important than ever to improve care and treatment for those left behind.”
CF is a rare but devastating disease caused by genetic mutations in a single gene, called CFTR. This gene codes for a pore, or channel, in cell membranes that allows water and chloride ions to enter and exit cells. Mutations in the CFTR gene can compromise the function of these channel proteins, leading to thickening of mucus and ensuing infections in the lungs and intestines of affected individuals.
Decades ago, most CF sufferers died by the age of five, but thanks to medical advances, including recently approved drugs known as CFTR modulators – which improve the function of the faulty channel proteins that result from CFTR gene mutations – the average life expectancy in CF today is 44 years.
McGarry first encountered the genetic differences between white and non-white CF patients in 2019 while working on a study in Puerto Rico with Esteban Burchard, MD, MPH, a pulmonologist and professor of bioengineering and therapeutic sciences at UCSF. They were investigating why 25 percent of Puerto Rican CF patients consistently test negative on standard CF screenings. After sequencing the genomes of 21 Puerto Rican and 61 Dominican CF patients they found that the most common CF mutations recognized in the United States were quite rare in these populations, findings which suggested that there was a limited understanding in the medical community of the range of possible CFTR mutations.
The new study confirms and expands upon these findings. Using the Cystic Fibrosis Foundation’s patient registry, which catalogs all the CF patients in the United States, McGarry and McColley analyzed how many patients had genetic mutations that confer eligibility for CFTR modulator drugs based on their U.S. Census-defined racial group. They found wide disparities in eligibility for the various groups, with about 94 percent of non-Hispanic white patients eligible for the drugs, but only about 75 percent of Hispanic patients and 70 percent of Black patients meeting current screening guidelines.
These numbers are not surprising considering that the clinical trials for CF modulators included almost exclusively non-Hispanic white participants. For example, in clinical trials for the drugs elexacaftor, tezacaftor and ivacaftor, the number of Black, Hispanic and Asian patients combined made up only around five percent of total trial participants.
“Drug companies sought approval for these drugs based solely on the most common CF mutations overall, because the bulk of CF patients are non-Hispanic white,” said McGarry. “But that’s not how we should be allocating drugs for rare, life-threatening diseases in children.”
McGarry and McColley also analyzed a measurement of lung function used to assess symptoms in CF patients called forced expiratory volume, or FEV1. They found that patients who took CFTR modulators had better FEV1 results regardless of their specific mutation. In a previous study, McGarry demonstrated that even patients without any of the required CF mutations still experienced improved pulmonary benefits from CFTR modulators, demonstrating that these drugs can benefit many more patients than just those with mutations approved by the FDA.
“This is a cautionary tale of how not to do precision medicine,” said McGarry. “Right now, we’re widening disparities and we don’t have a path to correct it.”
McGarry contends that the way in which clinical trials recruit participants is a form of structural racism. Researchers often seek out trial participants locally, which is a problem if the community is majority non-Hispanic white. If researchers do want more diverse participants, they often need to pay for translation, transportation costs, and lost wages. McGarry said that researchers should be including these costs in their grant applications and thinking more broadly about diversity in all aspects of their work.
“If you want to have minorities in your study, your research team should not be all non-Hispanic white,” said McGarry.
Funding: McGarry was supported by grants provided by the National Heart, Lung, and Blood Institute, and the Cystic Fibrosis Foundation Therapeutics Lab. McColley was supported by the Northwestern University Clinical and Translational Sciences Institute and the Cystic Fibrosis Foundation.
Research at Ann & Robert H. Lurie Children’s Hospital of Chicago is conducted through the Stanley Manne Children’s Research Institute. The Manne Research Institute is focused on improving child health, transforming pediatric medicine and ensuring healthier futures through the relentless pursuit of knowledge. Lurie Children’s is ranked as one of the nation’s top children’s hospitals by U.S. News & World Report. It is the pediatric training ground for Northwestern University Feinberg School of Medicine. Last year, the hospital served more than 220,000 children from 48 states and 49 countries.