# Radiomic Analysis in Contrast-Enhanced Spectral Mammography for Predicting Breast Cancer Histological Outcome

**Authors:** Daniele La Forgia, Annarita Fanizzi, Francesco Campobasso, Roberto Bellotti, Vittorio Didonna, Vito Lorusso, Marco Moschetta, Raffaella Massafra, Pasquale Tamborra, Sabina Tangaro, Michele Telegrafo, Maria Irene Pastena, Alfredo Zito

PMC · DOI: 10.3390/diagnostics10090708 · Diagnostics · 2020-09-17

## TL;DR

This study explores how radiomic features from Contrast-Enhanced Spectral Mammography can predict breast cancer histological outcomes and molecular subtypes.

## Contribution

The study introduces a novel application of radiomic analysis in CESM to predict specific breast cancer subtypes and histological markers.

## Key findings

- Radiomic features from CESM images were significantly correlated with ER, PR, Ki67, and HER2 markers.
- High accuracy was achieved in differentiating molecular subtypes like HER2+/HER2− and ER+/ER−.
- Results suggest CESM-based radiomics could be a valuable tool for predicting tumor characteristics.

## Abstract

Contrast-Enhanced Spectral Mammography (CESM) is a recently introduced mammographic method with characteristics particularly suitable for breast cancer radiomic analysis. This work aims to evaluate radiomic features for predicting histological outcome and two cancer molecular subtypes, namely Human Epidermal growth factor Receptor 2 (HER2)-positive and triple-negative. From 52 patients, 68 lesions were identified and confirmed on histological examination. Radiomic analysis was performed on regions of interest (ROIs) selected from both low-energy (LE) and ReCombined (RC) CESM images. Fourteen statistical features were extracted from each ROI. Expression of estrogen receptor (ER) was significantly correlated with variation coefficient and variation range calculated on both LE and RC images; progesterone receptor (PR) with skewness index calculated on LE images; and Ki67 with variation coefficient, variation range, entropy and relative smoothness indices calculated on RC images. HER2 was significantly associated with relative smoothness calculated on LE images, and grading tumor with variation coefficient, entropy and relative smoothness calculated on RC images. Encouraging results for differentiation between ER+/ER−, PR+/PR−, HER2+/HER2−, Ki67+/Ki67−, High-Grade/Low-Grade and TN/NTN were obtained. Specifically, the highest performances were obtained for discriminating HER2+/HER2− (90.87%), ER+/ER− (83.79%) and Ki67+/Ki67− (84.80%). Our results suggest an interesting role for radiomics in CESM to predict histological outcomes and particular tumors’ molecular subtype.

## Linked entities

- **Genes:** EREG (epiregulin) [NCBI Gene 2069], PGR (progesterone receptor) [NCBI Gene 5241], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** lymph vessel (MESH:C536223), TN (MESH:C562719), Breast Cancer (MESH:D001943), Tumor (MESH:D009369), allergic diathesis (MESH:D004198), -invasive carcinoma (MESH:D009361), breast lesions (MESH:D061325), lymph nodes metastasis (MESH:D008207), CESM (MESH:C564835), Ductal carcinoma in situ (MESH:D002285), allergic skin reaction (MESH:D004342), lymph node (MESH:D000072717), Invasive ductal carcinoma (MESH:D044584), Infiltrating lobular carcinoma (MESH:D018275), breast disease (MESH:D001941)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC7555402/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC7555402/full.md

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Source: https://tomesphere.com/paper/PMC7555402