Associations between Radiomics and Genomics in Non-Small Cell Lung Cancer Utilizing Computed Tomography and Next-Generation Sequencing: An Exploratory Study

Author:

Ottaiano Alessandro1ORCID,Grassi Francesca2,Sirica Roberto3ORCID,Genito Emanuela2ORCID,Ciani Giovanni2,Patanè Vittorio2ORCID,Monti Riccardo2,Belfiore Maria Paola2ORCID,Urraro Fabrizio2,Santorsola Mariachiara1,Ponsiglione Alfonso Maria4ORCID,Montella Marco5ORCID,Cappabianca Salvatore2,Reginelli Alfonso2ORCID,Sansone Mario4,Savarese Giovanni3,Grassi Roberta2

Affiliation:

1. Istituto Nazionale Tumori di Napoli, IRCCS “G. Pascale”, 80131 Naples, Italy

2. Department of Precision Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, 80138 Naples, Italy

3. AMES—Centro Polidiagnostico Strumentale, SRL, 80013 Naples, Italy

4. Department of Electrical Engineering and Information Technology, University of Naples “Federico II”, 80125 Naples, Italy

5. Pathology Unit, Department of Mental and Physical Health and Preventive Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, 80138 Naples, Italy

Abstract

Background: Radiomics, an evolving paradigm in medical imaging, involves the quantitative analysis of tumor features and demonstrates promise in predicting treatment responses and outcomes. This study aims to investigate the predictive capacity of radiomics for genetic alterations in non-small cell lung cancer (NSCLC). Methods: This exploratory, observational study integrated radiomic perspectives using computed tomography (CT) and genomic perspectives through next-generation sequencing (NGS) applied to liquid biopsies. Associations between radiomic features and genetic mutations were established using the Area Under the Receiver Operating Characteristic curve (AUC-ROC). Machine learning techniques, including Support Vector Machine (SVM) classification, aim to predict genetic mutations based on radiomic features. The prognostic impact of selected gene variants was assessed using Kaplan–Meier curves and Log-rank tests. Results: Sixty-six patients underwent screening, with fifty-seven being comprehensively characterized radiomically and genomically. Predominantly males (68.4%), adenocarcinoma was the prevalent histological type (73.7%). Disease staging is distributed across I/II (38.6%), III (31.6%), and IV (29.8%). Significant correlations were identified with mutations of ROS1 p.Thr145Pro (shape_Sphericity), ROS1 p.Arg167Gln (glszm_ZoneEntropy, firstorder_TotalEnergy), ROS1 p.Asp2213Asn (glszm_GrayLevelVariance, firstorder_RootMeanSquared), and ALK p.Asp1529Glu (glcm_Imc1). Patients with the ROS1 p.Thr145Pro variant demonstrated markedly shorter median survival compared to the wild-type group (9.7 months vs. not reached, p = 0.0143; HR: 5.35; 95% CI: 1.39–20.48). Conclusions: The exploration of the intersection between radiomics and cancer genetics in NSCLC is not only feasible but also holds the potential to improve genetic predictions and enhance prognostic accuracy.

Funder

Univeristà degli Studi della Campania "L. Vanvitelli"

Publisher

MDPI AG

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