
A greater understanding of patients with human epidermal growth factor receptor 2 (HER2)-mutated non-small cell lung cancer (NSCLC) and the associated tumor biology is critical for developing effective therapies, but information on real-world outcomes has been limited. Results from a study that analyzed real-world characteristics and outcomes among patients with HER2-mutated NSCLC from the US-based, deidentified Flatiron Health and Foundation Medicine’s Clinico-Genomic Database were presented at the 2023 North America Conference on Lung Cancer.
The researchers found that among 11,794 adults with advanced NSCLC between 2015 and 2021, 550 had a HER2 mutation (prevalence, 4.7%). The median age at diagnosis was 69.2 years, and 66.9% had a HER2 mutation type in the tyrosine kinase domain (TKD); 70.7% had a non-TKD mutation. In addition, half of the patients were female, 25.4% were never-smokers, and 65.3% were White.
Results showed that patients with a TKD mutation (n=200; 1.7%) tended to be female (60% vs 44% of non-TKD [n=346; 2.9%]) and never-smokers (44% vs 15% of non-TKD). The researchers also found they had lower tumor mutational burden (TMB; 75% of TKD vs 39% of non-TKD, with TMB <10 mutations/Mb). Results showed the most common HER2 variant was A775_G776insYVMA (n=95).