Identifying Genetic Mutation Status in Patients with Colorectal Cancer Liver Metastases Using Radiomics-Based Machine-Learning Models

Author:

Wesdorp Nina12,Zeeuw Michiel12ORCID,van der Meulen Delanie12ORCID,van ‘t Erve Iris3ORCID,Bodalal Zuhir4,Roor Joran5,van Waesberghe Jan Hein26,Moos Shira26,van den Bergh Janneke26,Nota Irene26,van Dieren Susan27ORCID,Stoker Jaap28ORCID,Meijer Gerrit3,Swijnenburg Rutger-Jan27,Punt Cornelis910,Huiskens Joost12,Beets-Tan Regina4,Fijneman Remond3ORCID,Marquering Henk2811,Kazemier Geert12,

Affiliation:

1. Department of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands

2. Cancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands

3. Department of Pathology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands

4. Department of Radiology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands

5. Department of Health, SAS Institute B.V., 1272 PC Huizen, The Netherlands

6. Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands

7. Department of Surgery, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands

8. Department of Radiology and Nuclear Medicine, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands

9. Department of Medical Oncology, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands

10. Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, 3584 CG Utrecht, The Netherlands

11. Department of Biomedical Engineering and Physics, Amsterdam UMC, University of Amsterdam, 1081 HV Amsterdam, The Netherlands

Abstract

For patients with colorectal cancer liver metastases (CRLM), the genetic mutation status is important in treatment selection and prognostication for survival outcomes. This study aims to investigate the relationship between radiomics imaging features and the genetic mutation status (KRAS mutation versus no mutation) in a large multicenter dataset of patients with CRLM and validate these findings in an external dataset. Patients with initially unresectable CRLM treated with systemic therapy of the randomized controlled CAIRO5 trial (NCT02162563) were included. All CRLM were semi-automatically segmented in pre-treatment CT scans and radiomics features were calculated from these segmentations. Additionally, data from the Netherlands Cancer Institute (NKI) were used for external validation. A total of 255 patients from the CAIRO5 trial were included. Random Forest, Gradient Boosting, Gradient Boosting + LightGBM, and Ensemble machine-learning classifiers showed AUC scores of 0.77 (95%CI 0.62–0.92), 0.77 (95%CI 0.64–0.90), 0.72 (95%CI 0.57–0.87), and 0.86 (95%CI 0.76–0.95) in the internal test set. Validation of the models on the external dataset with 129 patients resulted in AUC scores of 0.47–0.56. Machine-learning models incorporating CT imaging features could identify the genetic mutation status in patients with CRLM with a good accuracy in the internal test set. However, in the external validation set, the models performed poorly. External validation of machine-learning models is crucial for the assessment of clinical applicability and should be mandatory in all future studies in the field of radiomics.

Funder

Dutch Cancer Society

KWF project

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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