A High Percentage of NSCLC With Germline CHEK2 Mutation Harbors Actionable Driver Alterations: Survey of a Cancer Genomic Database and Review of Literature

INTRODUCTION: Germline CHEK2 mutations are rare and have not been associated with increased risk of NSCLC. METHODS: We identified two sequential primary NSCLCs harboring distinct actionable driver alterations (EGFR E746 _S752 delinsV and CD74-ROS1) in a patient with NSCLC with a novel germline CHEK2...

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Detalles Bibliográficos
Autores principales: Zhang, Shannon S., Lee, Jessica K., Tukachinsky, Hanna, Schrock, Alexa B., Nagasaka, Misako, Ou, Sai-Hong Ignatius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429789/
https://www.ncbi.nlm.nih.gov/pubmed/36061833
http://dx.doi.org/10.1016/j.jtocrr.2022.100387

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429789/
https://www.ncbi.nlm.nih.gov/pubmed/36061833
http://dx.doi.org/10.1016/j.jtocrr.2022.100387

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