Abstract
Radiomic features are potential imaging biomarkers for therapy response assessment in oncology. However, the robustness of features with respect to imaging parameters is not well established. Previously identified potential imaging biomarkers were found to be intrinsically dependent on voxel size and number of gray levels (GLs) in a recent texture phantom investigation. Here, we validate the voxel size and GL in-phantom normalizations in lung tumors. Eighteen patients with non-small cell lung cancer of varying tumor volumes were analyzed. To compare with patient data, phantom scans were acquired on eight different scanners. Twenty four previously identified features were extracted from lung tumors. The Spearman rank (rs) and interclass correlation coefficient (ICC) were used as metrics. Eight out of 10 features showed high (rs > 0.9) and low (rs < 0.5) correlations with number of voxels before and after normalizations, respectively. Likewise, texture features were unstable (ICC < 0.6) and highly stable (ICC > 0.8) before and after GL normalizations, respectively. We conclude that voxel size and GL normalizations derived from a texture phantom study also apply to lung tumors. This study highlights the importance and utility of investigating the robustness of radiomic features with respect to CT imaging parameters in radiomic phantoms.
Highlights
The extraction of quantitative information from medical images (Radiomics) holds great potential for cancer prediction and monitoring of therapy response[1,2,3]
The intensity-entropy and GLRLM-RLNU were independent of number of voxels after normalization, mostly reflecting information about the number of voxels inside the tumor volume before normalization
We showed that the voxel size and gray level normalization of CT radiomic features for lung cancer were in agreement with our previously reported findings using the Credence Cartridge Radiomic (CCR) phantom[8]
Summary
The extraction of quantitative information from medical images (Radiomics) holds great potential for cancer prediction and monitoring of therapy response[1,2,3]. The pixel size variation was 0.39 to 0.82 mm for 33 patients, but the author resampled the volumes to isotropic voxels of length 0.59 mm using cubic spline interpolation[13]. Since both reconstructed slice thickness and pixel size determine image voxel size or number of voxels within the tumor volume (VOI), it is important to investigate feature robustness as a function of number of voxels and voxel size within VOI. The robustness of texture features with different number of GLs significantly improves as a result of GL normalization[8]
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