Quantitative radiomic analysis in contrast-enhanced mammography for breast lesions characterisation
Author Block: G. Della Pepa1, C. Depretto1, W. Carli1, G. Irmici1, E. D'Ascoli1, C. De Berardinis1, C. Cazzella2, D. Ballerini1, G. P. Scaperrotta1; 1Milan/IT, 2Bergamo/IT
Purpose: This study aimed to investigate the potential of radiomic quantitative texture analysis for characterising breast lesions on contrast-enhanced mammography (CEM) and correlate them with their biological phenotypes.
Methods or Background: Patients who underwent CEM procedures at our institution since 2018 were considered. Among them, all CEM-detected malignant lesions, confirmed via core needle biopsy and surgical intervention, were included in our study.
These lesions were firstly subjected to a semi-automatic segmentation, and then 93 radiomic features were extracted for each of them, using the open-source Python package Py-Radiomics.
The association between each feature and the predetermined endpoints was evaluated through univariate logistic regression analysis. The correlation was performed either with the singular molecular characteristics: the presence of estrogen (ER) and progesterone (PR) receptors, HER2 status, Ki67 level either with the specific immunophenotype: Luminal A, Luminal B, HER2+ and Triple Negative (TN).
Results or Findings: In our preliminary results, 86 patients were selected, with a total of 89 breast lesions analysed. The logistic regression isolated a subset of radiomic features correlating robustly with the biological phenotype. Second-order statistics textural features of Neighbouring Gray Tone Difference Matrix (NGTDM) demonstrated a stronger correlation with the presence of both ER and PR receptors, and multiple combinations of them resulted in a better correlation with Luminal A and Luminal B immunophenotype. The Gray Level Run Length Matrix GLSZM contrast and first-order uniformity both correlate with the TN immunophenotype.
Conclusion: Radiomic quantitative texture analysis of breast lesions on CEM demonstrates promising capability in characterising biological phenotype. Looking forward, it could lead to the construction of a nomogram to be used in clinical practice, potentially helping decision-making processes before biopsy.
Limitations: The study is constrained by a limited sample size and by the lack of a distinct validation cohort.
Funding for this study: No funding was received for this study.
Has your study been approved by an ethics committee? Not applicable
Ethics committee - additional information: No information provided by the submitter.