A phase I/II study of osimertinib in EGFR exon 20 insertion mutation-positive non-small cell lung cancer

•Osimertinib 80 mg showed limited efficacy for NSCLC with EGFR ex20ins mutations.•The mutation type-specific concentration-dependency of osimertinibwas highlighted.•This study proposes higher dose osimertinib for NSCLC with EGFR ex20ins mutations. Several preclinical data proposed a potential effica...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2021-12, Vol.162, p.140-146
Hauptverfasser: Yasuda, Hiroyuki, Ichihara, Eiki, Sakakibara-Konishi, Jun, Zenke, Yoshitaka, Takeuchi, Shinji, Morise, Masahiro, Hotta, Katsuyuki, Sato, Mineyoshi, Matsumoto, Shingo, Tanimoto, Azusa, Matsuzawa, Reiko, Kiura, Katuyuki, Takashima, Yuta, Yano, Seiji, Koyama, Junji, Fukushima, Takahiro, Hamamoto, Junko, Terai, Hideki, Ikemura, Shinnosuke, Takemura, Ryo, Goto, Koichi, Soejima, Kenzo
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Sprache:eng
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Zusammenfassung:•Osimertinib 80 mg showed limited efficacy for NSCLC with EGFR ex20ins mutations.•The mutation type-specific concentration-dependency of osimertinibwas highlighted.•This study proposes higher dose osimertinib for NSCLC with EGFR ex20ins mutations. Several preclinical data proposed a potential efficacy of osimertinib, a third-generation EGFR tyrosine kinase inhibitor, for EGFR exon 20 insertion (EGFR ex20ins)-positive non-small cell lung cancer (NSCLC). However, reported case series and a retrospective study proposed controversial efficacy. The efficacy of osimertinib in EGFR ex20ins-positive NSCLC have not been well evaluated in prospective clinical trials. In this study, we performed a prospective, single-arm, multi-center, open-label, non-randomized phase I/II study to evaluate efficacy of osimertinib for EGFR ex20ins-positive NSCLC. From August 2018 to January 2020, 14 NSCLC patients with EGFR ex20ins were enrolled, of whom 2 were excluded because they did not meet the inclusion criteria. Efficacy and safety of 80 mg osimertinib were evaluated. In addition, we performed a translational exploratory study to clarify the association of mutation type-specific drug sensitivity, osimertinib pharmacokinetic data, and clinical efficacy. Of the evaluated patients, none experienced objective response, 7 experienced stable disease (58.3%), and 5 experienced disease progression (41.7%). The median progression free survival (PFS) was 3.8 months, and the median overall survival was 15.8 months. Interestingly, the exploratory study demonstrated statistically significant positive correlation between plasma osimertinib concentration/in vitro IC50 ratio and PFS (R = 0.9912, P = 0.0001), highlighting the mutation type-specific concentration-dependent efficacy of osimertinib for EGFR ex20ins-positive NSCLC. Regular dose, 80 mg/day, of osimertinib has limited clinical activity in NSCLC patients with EGFR ex20ins. The translational study proposed the potential efficacy of higher dose osimertinib in a subgroup of EGFR ex20ins-positive NSCLC.
ISSN:0169-5002
1872-8332
DOI:10.1016/j.lungcan.2021.10.006