Multiscale deep learning framework captures systemic immune features in lymph nodes predictive of triple negative breast cancer outcome in large‐scale studies

Author:

Verghese Gregory123,Li Mengyuan12ORCID,Liu Fangfang4,Lohan Amit5,Kurian Nikhil Cherian5,Meena Swati5,Gazinska Patrycja36,Shah Aekta17,Oozeer Aasiyah8,Chan Terry9ORCID,Opdam Mark9ORCID,Linn Sabine91011,Gillett Cheryl8,Alberts Elena12,Hardiman Thomas12,Jones Samantha12,Thavaraj Selvam1314,Jones J Louise12ORCID,Salgado Roberto1516,Pinder Sarah E2,Rane Swapnil17ORCID,Sethi Amit5ORCID,Grigoriadis Anita123ORCID

Affiliation:

1. Cancer Bioinformatics, School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences and Medicine King's College London London UK

2. School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences and Medicine King's College London London UK

3. Breast Cancer Now Unit, School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine King's College London London UK

4. Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education Key Laboratory of Cancer Prevention and Therapy Tianjin PR China

5. Department of Electrical Engineering Indian Institute of Technology Bombay Mumbai India

6. Biobank Research Group Lukasiewicz Research Network, PORT Polish Center for Technology Development Wroclaw Poland

7. Department of Pathology Tata Memorial Centre, Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

8. King's Health Partners Cancer Biobank, King's College London London UK

9. Division of Molecular Pathology The Netherlands Cancer Institute Amsterdam The Netherlands

10. Department of Medical Oncology The Netherlands Cancer Institute, Antoni van Leeuwenhoek Amsterdam The Netherlands

11. Department of Pathology University Medical Centre Utrecht The Netherlands

12. Centre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London London UK

13. Faculty of Dentistry, Oral & Craniofacial Science King's College London London UK

14. Head and Neck Pathology Guy's & St Thomas' NHS Foundation Trust London UK

15. Department of Pathology GZA‐ZNA Hospitals Antwerp Belgium

16. Division of Research Peter Mac Callum Cancer Centre Melbourne Australia

17. Department of Pathology Tata Memorial Centre‐ACTREC, HBNI Mumbai India

Abstract

AbstractThe suggestion that the systemic immune response in lymph nodes (LNs) conveys prognostic value for triple‐negative breast cancer (TNBC) patients has not previously been investigated in large cohorts. We used a deep learning (DL) framework to quantify morphological features in haematoxylin and eosin‐stained LNs on digitised whole slide images. From 345 breast cancer patients, 5,228 axillary LNs, cancer‐free and involved, were assessed. Generalisable multiscale DL frameworks were developed to capture and quantify germinal centres (GCs) and sinuses. Cox regression proportional hazard models tested the association between smuLymphNet‐captured GC and sinus quantifications and distant metastasis‐free survival (DMFS). smuLymphNet achieved a Dice coefficient of 0.86 and 0.74 for capturing GCs and sinuses, respectively, and was comparable to an interpathologist Dice coefficient of 0.66 (GC) and 0.60 (sinus). smuLymphNet‐captured sinuses were increased in LNs harbouring GCs (p < 0.001). smuLymphNet‐captured GCs retained clinical relevance in LN‐positive TNBC patients whose cancer‐free LNs had on average ≥2 GCs, had longer DMFS (hazard ratio [HR] = 0.28, p = 0.02) and extended GCs' prognostic value to LN‐negative TNBC patients (HR = 0.14, p = 0.002). Enlarged smuLymphNet‐captured sinuses in involved LNs were associated with superior DMFS in LN‐positive TNBC patients in a cohort from Guy's Hospital (multivariate HR = 0.39, p = 0.039) and with distant recurrence‐free survival in 95 LN‐positive TNBC patients of the Dutch‐N4plus trial (HR = 0.44, p = 0.024). Heuristic scoring of subcapsular sinuses in LNs of LN‐positive Tianjin TNBC patients (n = 85) cross‐validated the association of enlarged sinuses with shorter DMFS (involved LNs: HR = 0.33, p = 0.029 and cancer‐free LNs: HR = 0.21 p = 0.01). Morphological LN features reflective of cancer‐associated responses are robustly quantifiable by smuLymphNet. Our findings further strengthen the value of assessment of LN properties beyond the detection of metastatic deposits for prognostication of TNBC patients. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Funder

Breast Cancer Research Foundation

Breast Cancer Research Trust

China Scholarship Council

Cancer Research UK

Publisher

Wiley

Subject

Pathology and Forensic Medicine

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