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. 2025 May 13;25(1):159.
doi: 10.1186/s12880-025-01698-x.

Study on heterogeneity of vascularity and cellularity via multiparametric MRI habitat imaging in breast cancer

Affiliations

Study on heterogeneity of vascularity and cellularity via multiparametric MRI habitat imaging in breast cancer

Xiaolei Zhang et al. BMC Med Imaging. .

Abstract

Background: This study aimed to visually analyze the heterogeneity of vascularity and cellularity across different sub-regions of breast cancer using habitat imaging (HI) to predict human epidermal growth factor receptor 2 (HER2) expression and evaluate the effectiveness of neoadjuvant therapy (NAT) in breast cancer patients.

Methods: A retrospective analysis was conducted on 76 patients diagnosed with breast cancer. Diffusion-weighted imaging (DWI) and dynamic contrast-enhanced MRI (DCE-MRI) sequences were utilized to acquire MR images. Apparent diffusion coefficient (ADC), Ktrans, Kep, and Ve values were measured for each sub-region, and the percentage of each sub-region relative to the total lesion was calculated. Statistical analyses, including t-tests, rank-sum tests, chi-square tests, and Spearman correlation, were performed.

Results: Three distinct sub-regions within breast cancer lesions were identified through HI, characterized physiologically as: low vascularity-high cellularity (LV-HC), low vascularity-low cellularity (LV-LC), and high vascularity-low cellularity (HV-LC). Significant differences were observed in the proportions of these tumor sub-regions between HER2-positive and HER2-negative breast cancers. Additionally, HER2-low and HER2-zero breast cancers demonstrated statistical differences in the second sub-region (LV-LC). Furthermore, the proportion of the first sub-region (LV-HC) was negatively correlated with the efficacy of NAT in breast cancer patients.

Conclusions: Habitat imaging can identify distinct sub-regions within breast cancer lesions, providing a noninvasive imaging biomarker for predicting HER2 expression levels and assessing the efficacy of NAT in breast cancer patients.

Keywords: Breast cancer; HER2 expression; Habitat imaging; Multiparametric MRI; Tumor heterogeneity.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: Institutional Review Board approval was obtained. This study was approved by the Ethics Committee of the Second Affiliated Hospital of Shantou University Medical College (2020-34), which waived the requirement for written informed consent owing to the use of de-identified retrospective data. The authors confirm that all experiments involving humans and/or the use of human tissue samples were performed in accordance with the Declaration of Helsinki. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Flowchart of the study population
Fig. 2
Fig. 2
Image analysis and segmentation. a A 3D-slicer sketch map of the breast cancer focus VOI. b a multi-parameter MRI image registration map
Fig. 3
Fig. 3
Flowchart of FCM based lesions VOIs clustering
Fig. 4
Fig. 4
Three cases of breast cancer lesions. a Invasive ductal breast carcinoma (IHC 2+ with an amplified FISH assay). b Invasive ductal breast carcinoma (IHC 2+ with a non-amplified FISH assay). c Invasive ductal breast carcinoma (IHC 0)
Fig. 5
Fig. 5
An example of three divided spatial habitat sub-regions. a VOI of breast cancer lesions was sketched and aligned with quantitative parameter maps of ADC, ktrans, Ve and Kep. b FCM clustering algorithm was used to identify different habitat sub-regions of breast lesions

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References

    1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global Cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–49. - PubMed
    1. McDonald ES, Clark AS, Tchou J, Zhang P, Freedman GM. Clinical diagnosis and management of breast Cancer. J Nucl Med. 2016;57(Suppl 1):S9–16. - PubMed
    1. Pashayan N, Antoniou AC, Ivanus U, Esserman LJ, Easton DF, French D, Sroczynski G, Hall P, Cuzick J, Evans DG, et al. Personalized early detection and prevention of breast cancer: ENVISION consensus statement. Nat Rev Clin Oncol. 2020;17(11):687–705. - PMC - PubMed
    1. Bettaieb A, Paul C, Plenchette S, Shan J, Chouchane L, Ghiringhelli F. Precision medicine in breast cancer: reality or Utopia? J Transl Med. 2017;15(1):139. - PMC - PubMed
    1. Marusyk A, Polyak K. Tumor heterogeneity: causes and consequences. Biochim Biophys Acta. 2010;1805(1):105–17. - PMC - PubMed