4.5 Article

Analysis of tumor nuclear features using artificial intelligence to predict response to neoadjuvant chemotherapy in high-risk breast cancer patients

Journal

BREAST CANCER RESEARCH AND TREATMENT
Volume 186, Issue 2, Pages 379-389

Publisher

SPRINGER
DOI: 10.1007/s10549-020-06093-4

Keywords

Breast cancer; Neoadjuvant chemotherapy; Artificial intelligence; Digital pathology

Categories

Funding

  1. tri-council (Government of Canada) New Frontiers in Research Fund
  2. Terry Fox Research Institute
  3. Women's Health Golf Classic Foundation Fund
  4. Natural Sciences and Engineering Research Council of Canada
  5. York Research Chair in Quantitative Imaging and Smart Biomarkers

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The study aimed to predict response to neoadjuvant chemotherapy using artificial intelligence and found that tumor multifocality/multicentricity, nuclear intensity, and GLCM-COR were independently associated with likelihood of achieving a pathological complete response (pCR). The model was able to successfully classify 79% of cases.
Purpose Neoadjuvant chemotherapy (NAC) is used to treat patients with high-risk breast cancer. The tumor response to NAC can be classified as either a pathological partial response (pPR) or pathological complete response (pCR), defined as complete eradication of invasive tumor cells, with a pCR conferring a significantly lower risk of recurrence. Predicting the response to NAC, however, remains a significant clinical challenge. The objective of this study was to determine if analysis of nuclear features on core biopsies using artificial intelligence (AI) can predict response to NAC. Methods Fifty-eight HER2-positive or triple-negative breast cancer patients were included in this study (pCR n = 37, pPR n = 21). Multiple deep convolutional neural networks were developed to automate tumor detection and nuclear segmentation. Nuclear count, area, and circularity, as well as image-based first- and second-order features including mean pixel intensity and correlation of the gray-level co-occurrence matrix (GLCM-COR) were determined. Results In univariate analysis, the pCR group had fewer multifocal/multicentric tumors, higher nuclear intensity, and lower GLCM-COR compared to the pPR group. In multivariate binary logistic regression, tumor multifocality/multicentricity (OR = 0.14, p = 0.012), nuclear intensity (OR = 1.23, p = 0.018), and GLCM-COR (OR = 0.96, p = 0.043) were each independently associated with likelihood of achieving a pCR, and the model was able to successful classify 79% of cases (62% for pPR and 89% for pCR). Conclusion Analysis of tumor nuclear features using digital pathology/AI can significantly improve models to predict pathological response to NAC.

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