Quantification of intratumoral heterogeneity using habitat-based MRI radiomics to identify HER2-positive, -low and

Haoquan Chen1, Yulu Liu1,2, Jiaqi Zhao3

  • 1Department of Radiology, Peking University People's Hospital, No. 11, Xizhimen South St, Beijing, 100044, China.

PubMed
Abstract

Insights

Intratumoral heterogeneity (ITH) signatures effectively differentiate HER2-positive, HER2-low, and HER2-zero breast cancers using MRI radiomics. This approach aids in identifying patients who can benefit from HER2-targeted therapies.

Area of Science:

  • Oncology
  • Radiology
  • Biomedical Imaging

Background:

  • HER2-targeted therapy is effective for HER2-low breast cancer.
  • Intratumoral heterogeneity (ITH) complicates the identification of HER2-low tumors.
  • Quantifying ITH is crucial for accurate tumor classification.

Purpose of the Study:

  • To develop and validate ITH signatures for differentiating HER2 expression levels in breast cancer.
  • To assess the performance of radiomics and ITH signatures in classifying HER2-positive, HER2-low, and HER2-zero breast cancers.
  • To explore the utility of habitat-based MRI radiomics in capturing ITH.

Main Methods:

  • Retrospective study of 614 breast cancer patients.
  • Extraction of whole-tumor and habitat radiomics features from MRI.
  • Development of radiomics and ITH signatures.
  • Multivariable logistic regression and AUC analysis to evaluate model performance.

Main Results:

  • ITH signatures demonstrated high performance in differentiating HER2-positive/negative tumors (AUCs up to 0.83) and HER2-low/zero tumors (AUCs up to 0.94).
  • A combined model integrating clinicopathologic, radiomics, and ITH signatures improved classification accuracy.
  • Clinicopathologic characteristics were not significant predictors of HER2-low tumors.

Conclusions:

  • Habitat-based MRI radiomics can effectively quantify ITH.
  • Developed ITH signatures show significant promise for accurate breast cancer subtyping.
  • This method can improve patient selection for HER2-targeted therapies.

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