TY - JOUR A1 - Leger, Stefan A1 - Zwanenburg, Alex A1 - Leger, Karoline A1 - Lohaus, Fabian A1 - Linge, Annett A1 - Schreiber, Andreas A1 - Kalinauskaite, Goda A1 - Tinhofer, Inge A1 - Guberina, Nika A1 - Guberina, Maja A1 - Balermpas, Panagiotis A1 - Müller-von der Grün, Jens A1 - Ganswindt, Ute A1 - Belka, Claus A1 - Peeken, Jan Caspar A1 - Combs, Stephanie E. A1 - Boeke, Simon A1 - Zips, Daniel A1 - Richter, Christian A1 - Krause, Mechthild A1 - Baumann, Michael A1 - Troost, Esther Gera Cornelia A1 - Löck, Steffen T1 - Comprehensive analysis of tumour sub-volumes for radiomic risk modelling in locally advanced HNSCC T2 - Cancers N2 - Simple Summary: Radiomic risk models are usually based on imaging features, which are extracted from the entire gross tumour volume (GTV entire ). This approach does not explicitly consider the complex biological structure of the tumours. Therefore, in this retrospective study, we investigated the prognostic value of radiomic analyses based on different tumour sub-volumes using computed tomography imaging of patients with locally advanced head and neck squamous cell carcinoma who were treated with primary radio-chemotherapy. The GTV entire was cropped by different margins to define the rim and corresponding core sub-volumes of the tumour. Furthermore, the best performing tumour rim sub-volume was extended into surrounding tissue with different margins. As a result, the models based on the 5 mm tumour rim and on the 3 mm extended rim sub-volume showed an improved performance compared to models based on the corresponding tumour core. This indicates that the consideration of tumour sub-volumes may help to improve radiomic risk models. Abstract: Imaging features for radiomic analyses are commonly calculated from the entire gross tumour volume (GTVentire). However, tumours are biologically complex and the consideration of different tumour regions in radiomic models may lead to an improved outcome prediction. Therefore, we investigated the prognostic value of radiomic analyses based on different tumour sub-volumes using computed tomography imaging of patients with locally advanced head and neck squamous cell carcinoma. The GTVentire was cropped by different margins to define the rim and the corresponding core sub-volumes of the tumour. Subsequently, the best performing tumour rim sub-volume was extended into surrounding tissue with different margins. Radiomic risk models were developed and validated using a retrospective cohort consisting of 291 patients in one of the six Partner Sites of the German Cancer Consortium Radiation Oncology Group treated between 2005 and 2013. The validation concordance index (C-index) averaged over all applied learning algorithms and feature selection methods using the GTVentire achieved a moderate prognostic performance for loco-regional tumour control (C-index: 0.61 ± 0.04 (mean ± std)). The models based on the 5 mm tumour rim and on the 3 mm extended rim sub-volume showed higher median performances (C-index: 0.65 ± 0.02 and 0.64 ± 0.05, respectively), while models based on the corresponding tumour core volumes performed less (C-index: 0.59 ± 0.01). The difference in C-index between the 5 mm tumour rim and the corresponding core volume showed a statistical trend (p = 0.10). After additional prospective validation, the consideration of tumour sub-volumes may be a promising way to improve prognostic radiomic risk models. KW - radiomic KW - image-based risk modelling KW - machine learning KW - personalised therapy KW - radiation oncology Y1 - 2020 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/56537 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-565371 SN - 2072-6694 VL - 12 IS - 10, 3047 PB - MDPI CY - Basel ER -