ABSTRACT
BACKGROUND: Parameters of body composition have prognostic potential in patients with oncologic diseases. The aim of the present study was to analyse the prognostic potential of radiomics-based parameters of the skeletal musculature and adipose tissues in patients with advanced hepatocellular carcinoma (HCC). METHODS: Radiomics features were extracted from a cohort of 297 HCC patients as post hoc sub-study of the SORAMIC randomized controlled trial. Patients were treated with selective internal radiation therapy (SIRT) in combination with sorafenib or with sorafenib alone yielding two groups: (1) sorafenib monotherapy (n = 147) and (2) sorafenib and SIRT (n = 150). The main outcome was 1-year survival. Segmentation of muscle tissue and adipose tissue was used to retrieve 881 features. Correlation analysis and feature cleansing yielded 292 features for each patient group and each tissue type. We combined 9 feature selection methods with 10 feature set compositions to build 90 feature sets. We used 11 classifiers to build 990 models. We subdivided the patient groups into a train and validation cohort and a test cohort, that is, one third of the patient groups. RESULTS: We used the train and validation set to identify the best feature selection and classification model and applied it to the test set for each patient group. Classification yields for patients who underwent sorafenib monotherapy an accuracy of 75.51% and area under the curve (AUC) of 0.7576 (95% confidence interval [CI]: 0.6376-0.8776). For patients who underwent treatment with SIRT and sorafenib, results are accuracy = 78.00% and AUC = 0.8032 (95% CI: 0.6930-0.9134). CONCLUSIONS: Parameters of radiomics-based analysis of the skeletal musculature and adipose tissue predict 1-year survival in patients with advanced HCC. The prognostic value of radiomics-based parameters was higher in patients who were treated with SIRT and sorafenib.
ABSTRACT
BACKGROUND: For prediction of many types of clinical outcome, the skeletal muscle mass can be used as an independent biomarker. Manual segmentation of the skeletal muscles is time-consuming, therefore we present a deeplearning-based approach for the identification of muscle mass at the L3 level in clinical routine computed tomographic (CT) data. PATIENTS AND METHODS: We conducted a retrospective study of 130 patient datasets. Individual CT slice analysis at the L3 level was fed into a U-Net architecture. As a result, we obtained segmentations of the musculus rectus abdominis, abdominal wall muscles, musculus psoas major, musculus quadratus lumborum and musculus erector spinae in the CT-slice at the L3 level. RESULTS: The Dice score was 0.95±0.02, 0.86±0.12, 0.93±0.05, 0.92±0.05, 0.86±0.08 for the erector spine, rectus, abdominal wall, psoas and quadratus lumborum muscles, respectively. For the overall skeletal muscle mass, the test data achieved a Dice score of 0.95±0.03. CONCLUSION: Our network achieved Dice scores larger than 0.86 for each of the five different muscle types and 0.95 for the overall skeletal muscle mass. The subdivision of muscle types can serve as a basis for obtaining future biomarkers. Our network is publicly available so that it might be beneficial for others to improve the clinical workflow within examination of routine CT scans.