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DOI 10.1016/j.lungcan.2025.108479

Медицинская библиотека · Lung cancer (Amsterdam, Netherlands) · 2025

Efficacy of EGFR tyrosine kinase inhibitors in patients with non-small cell lung cancer with EGFR exon 19 insertions: clinical-genomic, preclinical analysis through LC-SCRUM-Asia (multi-institutional genomic screening registry).

Uehara Yuji, Izumi Hiroki, Kobayashi Ikei S, Matsumoto Shingo, Hosomi Yukio, Okuno Takae, Sugisaka Jun, Takase Naoto, Taima Kageaki, Sasaki Shinichi, Teranishi Shuhei, Miyamoto Shingo, Mori Masahide, Nakashima Chiho, Asano Shuichi, Oi Hajime, Sakai Tetsuya, Shibata Yuji, Udagawa Hibiki, Sugiyama Eri, Nosaki Kaname, Umemura Shigeki, Zenke Yoshitaka, Yoh Kiyotaka, Ikeda Sadakatsu, Costa Daniel B, Kobayashi Susumu S, Goto Koichi

СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

BACKGROUND

EGFR exon 19 insertions (EGFRex19ins) are rare EGFR mutations. Their clinical-genomic characteristics and outcomes with EGFR-tyrosine kinase inhibitors (TKIs) remain uncertain.

METHODS

We evaluated the clinical-genomic characteristics and outcomes of EGFR-TKIs for EGFRex19ins in the multi-institutional prospective lung cancer genomic screening project (LC-SCRUM-Asia). We also studied preclinical Ba/F3 models expressing EGFR-K745_E746insIPVAIK (Ba/F3-IPVAIK) to investigate their sensitivity to 1st-, 2nd-, 3rd-generation, and EGFR exon 20 insertion-active TKIs.

RESULTS

In LC-SCRUM-Asia, 16,204 NSCLC patients were enrolled from March 2015 to December 2023. EGFRex19ins were detected in 13 samples (0.1 % of NSCLC). The median age was 72 years (range, 38-80); most patients were female (77 %), had adenocarcinoma (92 %), and were never-smokers (62 %). Twelve patients (93 %) had EGFR-K745_E746insIPVAIK, while one (7 %) had EGFR-K745_E746insVPVAIK. The most frequent co-mutation was TP53 (62 %); no patients had other driver alterations. Six patients (46 %) tested positive for EGFR exon 19 deletions with PCR-based Cobas EGFR test, likely due to cross-reactivity arising from sequence homology. Twelve patients received EGFR-TKIs; five (42 %) experienced partial response. In the preclinical study, Ba/F3-IPVAIK showed the highest sensitivity to 2nd-generation EGFR-TKIs compared to other EGFR-TKIs. Structural studies supported these consistent results. When broken down by EGFR-TKI generations, response rates for 1st-, 2nd-, and 3rd-generation TKIs were 50 % (1/2), 80 % (4/5), and 0 % (0/5), respectively. The median PFS for 1st-, 2nd-, and 3rd-generation TKIs were 8.7 (95 % CI, 7.4-NR), 14.7 (95 % CI, 8.0-NR), and 4.4 (95 % CI, 3.4-NR) months, respectively.

CONCLUSION

Our preclinical, structural, and clinical findings indicate 2nd-generation EGFR-TKIs are more effective for EGFRex19ins compared to other TKIs.

Для цитирования: Uehara Yuji, Izumi Hiroki, Kobayashi Ikei S, Matsumoto Shingo, Hosomi Yukio, Okuno Takae, Sugisaka Jun, Takase Naoto, Taima Kageaki, Sasaki Shinichi, Teranishi Shuhei, Miyamoto Shingo, Mori Masahide, Nakashima Chiho, Asano Shuichi, Oi Hajime, Sakai Tetsuya, Shibata Yuji, Udagawa Hibiki, Sugiyama Eri, Nosaki Kaname, Umemura Shigeki, Zenke Yoshitaka, Yoh Kiyotaka, Ikeda Sadakatsu, Costa Daniel B, Kobayashi Susumu S, Goto Koichi. Efficacy of EGFR tyrosine kinase inhibitors in patients with non-small cell lung cancer with EGFR exon 19 insertions: clinical-genomic, preclinical analysis through LC-SCRUM-Asia (multi-institutional genomic screening registry).. Lung cancer (Amsterdam, Netherlands). 2025. DOI: 10.1016/j.lungcan.2025.108479.

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