Abstract

Tertiary lymphoid structures (TLS) are ectopic aggregates of lymphoid cells in inflamed, infected, or tumoral tissues that are easily recognized on an H&E histology slide as discrete entities, distinct from lymphocytes. TLS are associated with improved cancer prognosis but there is no standardised method available to quantify their presence. Previous studies have used immunohistochemistry to determine the presence of specific cells as a marker of the TLS. This has now been proven to be an underestimate of the true number of TLS. Thus, we propose a methodology for the automated identification and quantification of TLS, based on H&E slides. We subsequently determined the mathematical criteria defining a TLS. TLS regions were identified through a deep convolutional neural network and segmentation of lymphocytes was performed through an ellipsoidal model. This methodology had a 92.87% specificity at 95% sensitivity, 88.79% specificity at 98% sensitivity and 84.32% specificity at 99% sensitivity level based on 144 TLS annotated H&E slides implying that the automated approach was able to reproduce the histopathologists’ assessment with great accuracy. We showed that the minimum number of lymphocytes within TLS is 45 and the minimum TLS area is 6,245μm2. Furthermore, we have shown that the density of the lymphocytes is more than 3 times those outside of the TLS. The mean density and standard deviation of lymphocytes within a TLS area are 0.0128/μm2 and 0.0026/μm2 respectively compared to 0.004/μm2 and 0.001/μm2 in non-TLS regions. The proposed methodology shows great potential for automated identification and quantification of the TLS density on digital H&E slides.

Highlights

  • Understanding the host immune response to cancer is a critical area of investigation

  • We aim to translate the visual recognition of Tertiary lymphoid structures (TLS) by histopathologists into a universally reproducible set of mathematical values for the standardisation of TLS recognition: area occupied by TLS, the minimum number of lymphocytes present and their density

  • Through the first dataset, we internally validated the efficiency for TLS identification of the proposed methodology by performing an ablation analysis and leave-one-out crossvalidation and through the second dataset we externally validated the generalizability of the proposed model in a different population

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Summary

Introduction

Understanding the host immune response to cancer is a critical area of investigation. This has resulted in the recent introduction of various immunotherapeutic drugs (targeting checkpoint inhibition) in the treatment of lung, renal and skin cancers. The host immune response is partly mediated by the Tertiary Lymphoid Structures (TLS) [1]. Tertiary lymphoid structures (TLS) identification and density assessment

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