Abstract

BackgroundPrecise prognostic and predictive variables allowing improved post-operative treatment stratification are missing in patients treated for stage II colon cancer (CC). Investigation of tumor infiltrating lymphocytes (TILs) may be rewarding, but the lack of a standardized analytic technique is a major concern. Manual stereological counting is considered the gold standard, but digital pathology with image analysis is preferred due to time efficiency. The purpose of this study was to compare manual stereological estimates of TILs with automatic counts obtained by image analysis, and at the same time investigate the heterogeneity of TILs.MethodsFrom 43 patients treated for stage II CC in 2002 three paraffin embedded, tumor containing tissue blocks were selected one of them representing the deepest invasive tumor front. Serial sections from each of the 129 blocks were immunohistochemically stained for CD3 and CD8, and the slides were scanned.Stereological estimates of the numerical density and area fraction of TILs were obtained using the computer-assisted newCAST stereology system. For the image analysis approach an app-based algorithm was developed using Visiopharm Integrator System software. For both methods the tumor areas of interest (invasive front and central area) were manually delineated by the observer.ResultsBased on all sections, the Spearman’s correlation coefficients for density estimates varied from 0.9457 to 0.9638 (p < 0.0001), whereas the coefficients for area fraction estimates ranged from 0.9400 to 0.9603 (P < 0.0001). Regarding heterogeneity, intra-class correlation coefficients (ICC) for CD3+ TILs varied from 0.615 to 0.746 in the central area, and from 0.686 to 0.746 in the invasive area. ICC for CD8+ TILs varied from 0.724 to 0.775 in the central area, and from 0.746 to 0.765 in the invasive area.ConclusionsExact objective and time efficient estimates of numerical densities and area fractions of CD3+ and CD8+ TILs in stage II colon cancer can be obtained by image analysis and are highly correlated to the corresponding estimates obtained by the gold standard based on stereology. Since the intra-tumoral heterogeneity was low, this method may be recommended for quantifying TILs in only one histological section representing the deepest invasive tumor front.

Highlights

  • Precise prognostic and predictive variables allowing improved post-operative treatment stratification are missing in patients treated for stage II colon cancer (CC)

  • Heterogeneity Overall we found a tendency of higher densities of both CD3+ and CD8+ tumor infiltrating lymphocytes (TILs) in the invasive area compared to the central area

  • In this study we quantified CD3+ and CD8+ TILs using stereology and image analysis in adenocarcinomas of the colon, and we investigated the intra-tumoral heterogeneity of TILs

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Summary

Introduction

Precise prognostic and predictive variables allowing improved post-operative treatment stratification are missing in patients treated for stage II colon cancer (CC). For a more precise classification of the tumors as well as a better estimation of prognosis, new biomarkers are needed in addition to the current histological grading and the Tumor-Node-Metastasis (TNM) staging system. In this context, tumor infiltrating lymphocytes (TILs) have been analyzed in various settings, and several studies have shown promising results [3]. Numerous inflammatory cells are known to infiltrate malignant tumors, and are considered to be a manifestation of an immunological host reaction against cancer cells, reflecting a tumor-related immune response The majority of these cells are T-lymphocytes, and in particular cytotoxic T cells

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