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Mutational Profile from Targeted NGS Predicts Survival in LDCT Screening-Detected Lung Cancers.


ABSTRACT: BACKGROUND:The issue of overdiagnosis in low-dose computed tomography (LDCT) screening trials could be addressed by the development of complementary biomarkers able to improve detection of aggressive disease. The mutation profile of LDCT screening-detected lung tumors is currently unknown. METHODS:Targeted next-generation sequencing was performed on 94 LDCT screening-detected lung tumors. Associations with clinicopathologic features, survival, and the risk profile of a plasma microRNA signature classifier were analyzed. RESULTS:The mutational spectrum and frequency observed in screening series was similar to that reported in public data sets, although a larger number of tumors without mutations in driver genes was detected. The 5-year overall survival (OS) rates of patients with and without mutations in the tumors were 66% and 100%, respectively (p = 0.015). By combining the mutational status with the microRNA signature classifier risk profile, patients were stratified into three groups with 5-year OS rates ranging from 42% to 97% (p < 0.0001) and the prognostic value was significant after controlling for stage (p = 0.02). CONCLUSION:Tumor mutational status along with a microRNA-based liquid biopsy can provide additional information in planning clinical follow-up in lung cancer LDCT screening programs.

SUBMITTER: Verri C 

PROVIDER: S-EPMC6832691 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Mutational Profile from Targeted NGS Predicts Survival in LDCT Screening-Detected Lung Cancers.

Verri Carla C   Borzi Cristina C   Holscher Todd T   Dugo Matteo M   Devecchi Andrea A   Drake Katherine K   Sestini Stefano S   Suatoni Paola P   Romeo Elisa E   Sozzi Gabriella G   Pastorino Ugo U   Boeri Mattia M  

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 20170314 6


<h4>Background</h4>The issue of overdiagnosis in low-dose computed tomography (LDCT) screening trials could be addressed by the development of complementary biomarkers able to improve detection of aggressive disease. The mutation profile of LDCT screening-detected lung tumors is currently unknown.<h4>Methods</h4>Targeted next-generation sequencing was performed on 94 LDCT screening-detected lung tumors. Associations with clinicopathologic features, survival, and the risk profile of a plasma micr  ...[more]

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