Updated
Updated · The New York Times · Sep 17
Dana-Farber, 23andMe Find Gene That Raises Nonsmoker Lung Cancer Risk 62-Fold
Updated
Updated · The New York Times · Sep 17

Dana-Farber, 23andMe Find Gene That Raises Nonsmoker Lung Cancer Risk 62-Fold

3 articles · Updated · The New York Times · Sep 17

Summary

  • A Science study identified the inherited EGFR T790M mutation as a major driver of lung cancer in people who never smoked, with carriers facing a 62-fold higher risk.
  • The mutation is rare—about 1 in 15,850 people—but researchers called it among the strongest cancer-risk variants known and unusual because it is tied only to lung cancer.
  • Using 23andMe data, the team traced the variant largely to U.S. residents, especially in Southern Appalachia, with Tennessee and Alabama standing out after a founder event 200 to 225 years ago.
  • For carriers, the finding could support earlier screening, treatment and possibly prevention, while giving researchers a new window into how lung cancer develops in nonsmokers.

Insights

Will discovering this 62-fold cancer risk in non-smokers finally force the medical community to rewrite lung screening rules?
Are hidden environmental triggers like radon secretly activating this rare Appalachian lung cancer gene in people who never smoked?