Driver oncogenes in Sub-Saharan African patients with non-small cell lung cancer.

Lung Cancer (Auckl)

Department of Pulmonology, Centre Hospitalier Universitaire Saint Pierre; Faculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium.

Published: November 2016

AI Article Synopsis

  • Non-small cell lung cancer can have specific driver oncogenes like EGFR and ALK that could be targeted for therapy, with their prevalence varying by race, smoking habits, and gender.
  • Most research on these oncogenes has focused on Caucasian and Asian populations, with little to no existing data on Sub-Saharan African patients where smoking is less prevalent.
  • In a small case study of six Sub-Saharan African patients with advanced lung adenocarcinoma, a significant number had EGFR mutations (3/6) or ALK rearrangement (1/6), suggesting that the lower smoking rates in this group may be linked to a higher prevalence of these driver mutations.

Article Abstract

Non-small cell lung cancer can exhibit driver oncogenes, including epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK), that are possible targets for therapy. The prevalence of these rearranged driver oncogenes is influenced by race, smoking habits, and gender. Most data come from Caucasian and Asian populations. To our knowledge, there is no literature available about the prevalence of driver oncogenes in Sub-Saharan Africa, where the tobacco epidemic is still in the early stage. In this small case series, 6 patients of Sub-Saharan African ethnicity with stage IV lung adenocarcinoma are described. EGFR mutation was present in 3/6 patients and ALK rearrangement in 1/6 patients. This incidence seems high but interestingly, all patients were non-smokers or light smokers. In this series, the high prevalence of driver oncogene was probably related to low smoking habits and these initial data in Sub-Saharan Africans suggest high prevalence of driver mutations for this reason.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310716PMC
http://dx.doi.org/10.2147/LCTT.S116762DOI Listing

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