Thoracic Cancer (Nov 2022)

Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring EGFR L858R and L747V mutations

  • Mio Kanbe,
  • Noriaki Sunaga,
  • Kenichiro Hara,
  • Hiiru Sawada,
  • Ikuo Wakamatsu,
  • Kentaro Hara,
  • Sohei Muto,
  • Yuri Sawada,
  • Hiroaki Masubuchi,
  • Mari Sato,
  • Yosuke Miura,
  • Hiroaki Tsurumaki,
  • Masakiyo Yatomi,
  • Reiko Sakurai,
  • Yasuhiko Koga,
  • Yoichi Ohtaki,
  • Toshiteru Nagashima,
  • Naoko Okano,
  • Nobuteru Kubo,
  • Toshitaka Maeno,
  • Takeshi Hisada

DOI
https://doi.org/10.1111/1759-7714.14678
Journal volume & issue
Vol. 13, no. 22
pp. 3225 – 3228

Abstract

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Abstract Epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitors are standard therapeutic agents for non‐small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to be fully established. Here, we report a long‐term (≥20 years from initial diagnosis) NSCLC survivor carrying EGFR L858R and L747V mutations. The patient received gefitinib monotherapy, systemic chemotherapy/chemoimmunotherapy, and local consolidative therapies for oligometastatic lesions, and responded to afatinib rechallenge with a progression‐free survival of 12 months. The current case suggests that afatinib is effective in NSCLC patients with EGFR L858R and L747V mutations and that a therapeutic approach combining appropriately timed systemic therapies with local consolidative therapies for oligometastatic lesions improves long‐term survival.

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