| Literature DB >> 32354946 |
Gen Ohara1, Shinichiro Okauchi1, Yuika Sasatani1, Toshihiro Shiozawa2, Hideyasu Yamada3, Kunihiko Miyazaki4, Hiroaki Satoh5.
Abstract
BACKGROUND: In the majority of non-small cell lung cancer (NSCLC) patients with uncommon EGFR mutations, first generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are ineffective. The second-generation TKI, afatinib, is considered effective in patients with uncommon mutations, however, long-term survivors have been rare. CASE REPORT: We report herein a patient with lung adenocarcinoma harboring double uncommon EGFR L861Q and G719X mutations, who is free of disease 32 months after initiation of afatinib therapy. To our best knowledge, this patient has the longest response among other patients with double uncommon mutations.Entities:
Keywords: Long-term survival; afatinib; lung adenocarcinoma; uncommon EGFR mutations
Mesh:
Substances:
Year: 2020 PMID: 32354946 PMCID: PMC7279823 DOI: 10.21873/invivo.11929
Source DB: PubMed Journal: In Vivo ISSN: 0258-851X Impact factor: 2.155