Large-scale clinico-genomic profile of non-small cell lung cancer with KRAS G12C: Results from LC-SCRUM-Asia study

•The frequency of KRAS G12C was 4.0% in Asian patients with NSCLC.•KRAS G12C tumor had higher tumor mutation burden and higher PD-L1 expression.•KRAS G12C-positive NSCLC showed potential sensitivity to ICIs. KRAS G12C is an oncogenic driver mutation, accounting for approximately 14% of Caucasian pat...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2023-02, Vol.176, p.103-111
Hauptverfasser: Tamiya, Yutaro, Matsumoto, Shingo, Zenke, Yoshitaka, Yoh, Kiyotaka, Ikeda, Takaya, Shibata, Yuji, Kato, Terufumi, Nishino, Kazumi, Nakamura, Atsushi, Furuya, Naoki, Miyamoto, Shingo, Kuyama, Shoichi, Nomura, Shogo, Ikeno, Takashi, Udagawa, Hibiki, Sugiyama, Eri, Nosaki, Kaname, Izumi, Hiroki, Sakai, Tetsuya, Hashimoto, Naozumi, Goto, Koichi
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Sprache:eng
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Zusammenfassung:•The frequency of KRAS G12C was 4.0% in Asian patients with NSCLC.•KRAS G12C tumor had higher tumor mutation burden and higher PD-L1 expression.•KRAS G12C-positive NSCLC showed potential sensitivity to ICIs. KRAS G12C is an oncogenic driver mutation, accounting for approximately 14% of Caucasian patients with non-small cell lung cancer (NSCLC). Recently, several KRAS G12C-targeted drugs have been developed; however, the clinico-genomic characteristics of NSCLC patients with KRAS G12C remain unclear. Based on the large-scale prospective lung cancer genomic screening project (LC-SCRUM-Asia) database, the clinico-genomic characteristics and therapeutic outcomes of NSCLC patients with KRAS G12C were evaluated. From March 2015 to March 2021, 10,023 NSCLC patients were enrolled in LC-SCRUM-Asia. KRAS mutations were detected in 1258 patients (14 %), including G12C in 376 (4.0 %), G12D in 289 (3.1 %) and G12V in 251 (2.7 %). The proportions of males and smokers were higher in patients with KRAS G12C than in those with KRAS non-G12C mutations (males: 73 % vs 63 %, p 
ISSN:0169-5002
1872-8332
DOI:10.1016/j.lungcan.2022.12.019