| Literature DB >> 32179095 |
Bihong T Chen1, Taihao Jin2, Ningrong Ye2, Isa Mambetsariev3, Ebenezer Daniel2, Tao Wang4, Chi Wah Wong5, Russell C Rockne6, Rivka Colen7, Andrei I Holodny8, Sagus Sampath9, Ravi Salgia3.
Abstract
Lung cancer metastases comprise most of all brain metastases in adults and most brain metastases are diagnosed by magnetic resonance (MR) scans. The purpose of this study was to conduct an MR imaging-based radiomic analysis of brain metastatic lesions from patients with primary lung cancer to classify mutational status of the metastatic disease. We retrospectively identified lung cancer patients with brain metastases treated at our institution between 2009 and 2017 who underwent genotype testing of their primary lung cancer. Brain MR Images were used for segmentation of enhancing tumors and peritumoral edema, and for radiomic feature extraction. The most relevant radiomic features were identified and used with clinical data to train random forest classifiers to classify the mutation status. Of 110 patients in the study cohort (mean age 57.51 ± 12.32 years; M: F = 37:73), 75 had an EGFR mutation, 21 had an ALK translocation, and 15 had a KRAS mutation. One patient had both ALK translocation and EGFR mutation. Majority of radiomic features most relevant for mutation classification were textural. Model building using both radiomic features and clinical data yielded more accurate classifications than using either alone. For classification of EGFR, ALK, and KRAS mutation status, the model built with both radiomic features and clinical data resulted in area-under-the-curve (AUC) values based on cross-validation of 0.912, 0.915, and 0.985, respectively. Our study demonstrated that MR imaging-based radiomic analysis of brain metastases in patients with primary lung cancer may be used to classify mutation status. This approach may be useful for devising treatment strategies and informing prognosis.Entities:
Keywords: Brain metastases; Lung cancer; Mutation; Predictive modeling; Radiomics
Mesh:
Substances:
Year: 2020 PMID: 32179095 PMCID: PMC7237274 DOI: 10.1016/j.mri.2020.03.002
Source DB: PubMed Journal: Magn Reson Imaging ISSN: 0730-725X Impact factor: 2.546