Womens and Lung Cancer | African and American Womens lung cancer | Why African American lung cancer patients respond differently
lung cancer for Clinical research out of University Hospitals Case Medical Center has observed that African Americans with a common form of lung cancer have a lower frequency of drug-sensitizing genetic mutations, which may impact response to new cancer-fighting drugs. Published online in the Journal of Clinical Oncology, the study by Rom Leidner, MD, and his colleagues report that ethnicity plays a significant role in non-small cell lung cancer (NSCLC) genetics and more personalized therapys appears to be beneficial to cancer patients.
African American patients with NSCLC are significantly less likely than Caucasian counterparts to harbor activating mutations of the epidermal growth factor receptor (EGFR) gene in their cancers, which suggests that common oral EGFR inhibitor drugs, such as Tarceva (erlotinib), are unlikely to yield dramatic remissions. Additionally, cancer biopsy testing revealed that African American patients with NSCLC are significantly more likely to have increased copies of the EGFR gene than Caucasians. Detection of increased copies of the Her2 gene in breast cancer, a gene closely correlation to EGFR, has been the basis for major advances in treatment using drugs which target Her2.
“We are finding that ethnicity may play a significant role in a variety of cancers,” says Dr. Leidner, an oncologist with Ireland Cancer Center of University Hospitals Case Medical Center and Visiting Instructor at Case Western Reserve University School of Medicine. “It was already known that a higher proportion of East Asian NSCLC patients harbor mutations of the EGFR gene than Caucasians, and that these mutations are linked to a higher likelihood of major responses to EGFR inhibitors. Before our study, however, surprisingly little data existed for African American patients with this common type of lung cancer.”
These findings add to a growing body of evidence demonstrating genetic variation in genetic pathways between ethnic groups, and underscores the need for incorporation of these differences into the design of future clinical trials with agents targeting the EGFR pathway.
Epidemiologic studies have suggested that African Americans have a higher risk of NSCLC and have poorer outcomes with therapy. Ethnic background and genetic make-up are linked, and consequently, may impact the likelihood of major responses to oral EGFR inhibiting drugs. For example, in large international lung cancer trials a higher percentage of East Asian NSCLC patients were found to carry drug-sensitizing mutations of the EGFR gene than Caucasians, and as predicted the highest rates of response to EGFR inhibitor drugs were found in the East Asian patients.
The recently published findings have led the scientists to initiate a follow-up study. This multi-center effort will review the overall rates of response, or lack thereof, among African American patients with NSCLC treated at the Case Comprehensive Cancer Center with EGFR inhibitor drugs during the course of their illness.
“In the future, this may lead clinical cancer scientists to be able to take advantage of these findings for a ‘smart-design approach’ to clinical trials in lung cancer, with novel therapys and biomarkers employed among different patient populations or even individuals,” says Stanton Gerson, MD, Director of the University Hospitals Ireland Cancer Center as well as the Case Comprehensive Cancer Center. “Targeted therapys for patients based on a myriad of genetic and ethnic factors are the wave of the future and may lead the way to improved cure rates for our cancer patients”.