Clinically Interpretable Radiomics-Based Prediction of Histopathologic Response to Neoadjuvant Chemotherapy in High-Grade Serous Ovarian Carcinoma.
Authors
Rundo, Leonardo
Beer, Lucian
Escudero Sanchez, Lorena
Crispin-Ortuzar, Mireia
Reinius, Marika
McCague, Cathal
Sahin, Hilal
Bura, Vlad
Pintican, Roxana
Zerunian, Marta
Ursprung, Stephan
Allajbeu, Iris
Addley, Helen
Martin-Gonzalez, Paula
Buddenkotte, Thomas
Singh, Naveena
Sahdev, Anju
Funingana, Ionut-Gabriel
Jimenez-Linan, Mercedes
Brenton, James D
Woitek, Ramona
Publication Date
2022Journal Title
Front Oncol
ISSN
2234-943X
Publisher
Frontiers Media SA
Language
en
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Rundo, L., Beer, L., Escudero Sanchez, L., Crispin-Ortuzar, M., Reinius, M., McCague, C., Sahin, H., et al. (2022). Clinically Interpretable Radiomics-Based Prediction of Histopathologic Response to Neoadjuvant Chemotherapy in High-Grade Serous Ovarian Carcinoma.. Front Oncol https://doi.org/10.3389/fonc.2022.868265
Abstract
BACKGROUND: Pathological response to neoadjuvant treatment for patients with high-grade serous ovarian carcinoma (HGSOC) is assessed using the chemotherapy response score (CRS) for omental tumor deposits. The main limitation of CRS is that it requires surgical sampling after initial neoadjuvant chemotherapy (NACT) treatment. Earlier and non-invasive response predictors could improve patient stratification. We developed computed tomography (CT) radiomic measures to predict neoadjuvant response before NACT using CRS as a gold standard. METHODS: Omental CT-based radiomics models, yielding a simplified fully interpretable radiomic signature, were developed using Elastic Net logistic regression and compared to predictions based on omental tumor volume alone. Models were developed on a single institution cohort of neoadjuvant-treated HGSOC (n = 61; 41% complete response to NCT) and tested on an external test cohort (n = 48; 21% complete response). RESULTS: The performance of the comprehensive radiomics models and the fully interpretable radiomics model was significantly higher than volume-based predictions of response in both the discovery and external test sets when assessed using G-mean (geometric mean of sensitivity and specificity) and NPV, indicating high generalizability and reliability in identifying non-responders when using radiomics. The performance of a fully interpretable model was similar to that of comprehensive radiomics models. CONCLUSIONS: CT-based radiomics allows for predicting response to NACT in a timely manner and without the need for abdominal surgery. Adding pre-NACT radiomics to volumetry improved model performance for predictions of response to NACT in HGSOC and was robust to external testing. A radiomic signature based on five robust predictive features provides improved clinical interpretability and may thus facilitate clinical acceptance and application.
Keywords
chemotherapy response score, computed tomography, neoadjuvant chemotherapy, ovarian cancer, radiomics
Sponsorship
Engineering and Physical Sciences Research Council (EP/P020259/1)
Cancer Research UK (C96/A25177)
National Institute for Health Research (IS-BRC-1215-20014)
Wellcome Trust (215733/Z/19/Z)
Identifiers
External DOI: https://doi.org/10.3389/fonc.2022.868265
This record's URL: https://www.repository.cam.ac.uk/handle/1810/338626
Rights
Licence:
http://creativecommons.org/licenses/by/4.0/
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