Abstract
Purpose: To design and validate a preprocessing procedure dedicated to T2-weighted MR images of lung cancers so as to improve the ability of radiomic features to distinguish between adenocarcinoma and other histological types.Materials and Methods: A discovery set of 52 patients with advanced lung cancer who underwent T2-weighted MR imaging at 3 Tesla in a single center study from August 2017 to May 2019 was used. Findings were then validated using a validation set of 19 additional patients included from May to October 2019. Tumor type was obtained from the pathology report after trans-thoracic needle biopsy, metastatic lymph node or metastasis samples, or surgical excisions. MR images were preprocessed using N4ITK bias field correction and by normalizing voxel intensities with fat as a reference region. Segmentation and extraction of radiomic features were performed with LIFEx software on the raw images, on the N4ITK-corrected images and on the fully preprocessed images. Two analyses were conducted where radiomic features were extracted: (1) from the whole tumor volume (3D analysis); (2) from all slices encompassing the tumor (2D analysis). Receiver operating characteristic (ROC) analysis was used to identify features that could distinguish between adenocarcinoma and other histological types. Sham experiments were also designed to control the number of false positive findings.Results: There were 31 (12) adenocarcinomas and 21 (7) other histological types in the discovery (validation) set. In 2D, preprocessing increased the number of discriminant radiomic features from 8 without preprocessing to 22 with preprocessing. 2D analysis yielded more features able to identify adenocarcinoma than 3D analysis (12 discriminant radiomic features after preprocessing in 3D). Preprocessing did not increase false positive findings as no discriminant features were identified in any of the sham experiments. The greatest sensitivity of the 2D analysis applied to preprocessed data was confirmed in the validation set.Conclusion: Correction for magnetic field inhomogeneities and normalization of voxel values are essential to reveal the full potential of radiomic features to identify the tumor histological type from MR T2-weighted images, with classification performance similar to those reported in PET/CT and in multiphase CT in lung cancers.
Highlights
Radiomics consists in the extraction of a large number of quantitative features from radiology images to describe the shape, intensity distribution, and texture characteristics of a region of interest [1,2,3]
The other tumors (OTH) group contained a majority of squamous cell carcinoma (76%)
We investigated the potential of MRI radiomics for lung cancer assessment and demonstrated the need for careful preprocessing of MR images to identify radiomic features correlated with the tumor pathology
Summary
Radiomics consists in the extraction of a large number of quantitative features from radiology images to describe the shape, intensity distribution, and texture characteristics of a region of interest [1,2,3]. In oncology, radiomic features might reflect tumor heterogeneity observed at the histological and genetic levels [4]. The macroscopic heterogeneity corresponds to variations of image intensities between neighboring voxels, which are described by radiomic features. Radiomic features are expected to be related to the phenotype, genotype and microenvironment of the tumor, and be of interest to support therapeutic decisions [7]. Radiomics is largely investigated to assist cancer diagnosis, prognosis, and prediction of response to therapy [8, 9]
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