Literature DB >> 34246541

The Common Thread: A Case of Synchronous Lung Cancers and a Germline CHEK2 Mutation.

Edward T Carey1, Virginia Ferreira2, Elaine Shum2, Fang Zhou2, Joshua K Sabari2.   

Abstract

Patients with one form of cancer are at increased risk for another, and this is true for lung cancer, where synchronous primary lung cancers are an increasing multifaceted challenge.1,2 Here, we present the case of a middle age woman who was found to have bilateral lung masses. Biopsy and subsequent testing revealed unique synchronous lung adenocarcinomas, each with unique genetic signatures. Despite having two unique tumors, she was found to have CHEK2 mutations in both tumors and in germline testing. Because of this extensive testing that showed unique tumors, she was ultimately diagnosed with stage IIIb and IA2 lung cancers, and this changed her treatment options. Consideration of unique primary tumors leads to thorough diagnostics, which changed this patient's diagnosis, prognosis, and treatment. We hope this case raises awareness for multiple primary tumors, as well as CHEK2 as an important oncogene.
Copyright © 2021. Published by Elsevier Inc.

Entities:  

Keywords:  ChEK2 mutations; Germline mutations; KRAS; Lung adenocarcinoma; Multiple primary tumors

Mesh:

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Year:  2021        PMID: 34246541     DOI: 10.1016/j.cllc.2021.05.011

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  1 in total

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

Authors:  Shannon S Zhang; Jessica K Lee; Hanna Tukachinsky; Alexa B Schrock; Misako Nagasaka; Sai-Hong Ignatius Ou
Journal:  JTO Clin Res Rep       Date:  2022-08-06
  1 in total

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