Predicting Patterns of Distant Metastasis in Breast Cancer Patients following Local Regional Therapy Using Machine Learning

Author:

Shiner Audrey123ORCID,Kiss Alex4,Saednia Khadijeh15,Jerzak Katarzyna J.6,Gandhi Sonal6,Lu Fang-I7,Emmenegger Urban6ORCID,Fleshner Lauren123ORCID,Lagree Andrew2ORCID,Alera Marie Angeli2,Bielecki Mateusz12,Law Ethan2,Law Brianna2,Kam Dylan2,Klein Jonathan8,Pinard Christopher J.2,Shenfield Alex9ORCID,Sadeghi-Naini Ali15,Tran William T.12310ORCID

Affiliation:

1. Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada

2. Biological Sciences Platform, Sunnybrook Research Institute, Toronto, ON M4N 3M5, Canada

3. Institute of Medical Sciences, University of Toronto, Toronto, ON M5S 1A8, Canada

4. Institute of Clinical Evaluative Sciences, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada

5. Department of Electrical Engineering and Computer Science, Lassonde School of Engineering, York University, Toronto, ON M3J 1P3, Canada

6. Division of Medical Oncology, Department of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada

7. Department of Anatomic Pathology, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada

8. Department of Radiation Oncology, Albert Einstein College of Medicine, New York, NY 10461, USA

9. Department of Engineering and Mathematics, Sheffield Hallam University, Sheffield S1 1WB, UK

10. Department of Radiation Oncology, University of Toronto, Toronto, ON M5S 1A8, Canada

Abstract

Up to 30% of breast cancer (BC) patients will develop distant metastases (DM), for which there is no cure. Here, statistical and machine learning (ML) models were developed to estimate the risk of site-specific DM following local-regional therapy. This retrospective study cohort included 175 patients diagnosed with invasive BC who later developed DM. Clinicopathological information was collected for analysis. Outcome variables were the first site of metastasis (brain, bone or visceral) and the time interval (months) to developing DM. Multivariate statistical analysis and ML-based multivariable gradient boosting machines identified factors associated with these outcomes. Machine learning models predicted the site of DM, demonstrating an area under the curve of 0.74, 0.75, and 0.73 for brain, bone and visceral sites, respectively. Overall, most patients (57%) developed bone metastases, with increased odds associated with estrogen receptor (ER) positivity. Human epidermal growth factor receptor-2 (HER2) positivity and non-anthracycline chemotherapy regimens were associated with a decreased risk of bone DM, while brain metastasis was associated with ER-negativity. Furthermore, non-anthracycline chemotherapy alone was a significant predictor of visceral metastasis. Here, clinicopathologic and treatment variables used in ML prediction models predict the first site of metastasis in BC. Further validation may guide focused patient-specific surveillance practices.

Funder

Tri-Council (CIHR) Government of Canada’s New Frontiers in Research Fund

AMS Healthcare

TFRI

Natural Sciences and Engineering Research Council

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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