Abstract

Radiomics–the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly by differences in scan acquisition and reconstruction settings. Previous studies reported on the sensitivity of radiomic features (RFs) to test-retest variability, inter-observer segmentation variability, and intra-scanner variability. A framework involving robust radiomics analysis and the application of a post-reconstruction feature harmonization method using ComBat was recently proposed to address these challenges. In this study, we investigated the reproducibility of RFs across different scanners and scanning parameters using this framework. We analysed thirteen scans of a ten-layer phantom that were acquired differently. Each layer was subdivided into sixteen regions of interest (ROIs), and the scans were compared in a pairwise manner, resulting in seventy-eight different scenarios. Ninety-one RFs were extracted from each ROI. As hypothesized, we demonstrate that the reproducibility of a given RF is not a constant but is dependent on the heterogeneity found in the data under analysis. The number (%) of reproducible RFs varied across the pairwise scenarios investigated, having a wide range between 8 (8.8%) and 78 (85.7%) RFs. Furthermore, in contrast to what has been previously reported, and as hypothesized in the robust radiomics analysis framework, our results demonstrate that ComBat cannot be applied to all RFs but rather on a percentage of those–the “ComBatable” RFs–which differed depending on the data being harmonized. The number (%) of reproducible RFs following ComBat harmonization varied across the pairwise scenarios investigated, ranging from 14 (15.4%) to 80 (87.9%) RFs, and was found to depend on the heterogeneity in the data. We conclude that the standardization of image acquisition protocols remains the cornerstone for improving the reproducibility of RFs, and the generalizability of the signatures developed. Our proposed approach helps identify the reproducible RFs across different datasets.

Highlights

  • With the advancement and involvement of artificial intelligence in performing high-level tasks, its application has been extensively researched in the field of medical imaging analysis [1]

  • The Credence Cartridge Radiomics (CCR) phantom is composed of 10 different layers that correspond to different texture patterns spanning a range of −900 to +700 Hounsfield units (HU)

  • Combining Batches (ComBat) cannot be successfully applied on all radiomic features (RFs), and its successful application on a given RF is dependent on the heterogeneity of the dataset

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Summary

Introduction

With the advancement and involvement of artificial intelligence in performing high-level tasks, its application has been extensively researched in the field of medical imaging analysis [1]. The above-mentioned studies focused on the reproducibility of RFs in limited settings, such as test-retest, inter-observer variability, and intra-scanner variability. As these studies reported significant differences in groups of RFs, it is only intuitive that adding more variation to image acquisition and reconstruction will further dampen the reproducibility of RFs. As these studies reported significant differences in groups of RFs, it is only intuitive that adding more variation to image acquisition and reconstruction will further dampen the reproducibility of RFs These findings indicate that ignoring data heterogeneity will influence the performance and generalizability of the models developed, especially in studies where training and validation sets are independent. RFs that cannot be reproduced cannot be compared or selected as biomarkers

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