Prognostic Value of T-Cell Density in the Tumor Center and Outer Margins in Gastric Cancer

被引:6
作者
Soeratram, Tanya T. D. [1 ,2 ]
Biesma, Hedde D. [1 ,2 ]
Egthuijsen, Jacqueline M. P. [1 ,2 ]
Kranenbarg, Elma Meershoek-Klein [3 ]
Hartgrink, Henk H. [3 ]
van de Velde, Cornelis J. H. [3 ]
Mookhoek, Aart [4 ]
van Dijk, Erik [1 ,2 ]
Kim, Yongsoo [1 ,2 ]
Ylstra, Bauke [1 ,2 ]
van Laarhoven, Hanneke W. M. [2 ,5 ]
van Grieken, Nicole C. T. [1 ,2 ]
机构
[1] Vrije Univ Amsterdam, Dept Pathol, Amsterdam UMC, Amsterdam, Netherlands
[2] Canc Ctr Amsterdam Canc Biol & Immunol, Amsterdam, Netherlands
[3] Leiden Univ, Dept Surg, Med Ctr, Leiden, Netherlands
[4] Univ Bern, Dept Pathol, Bern, Switzerland
[5] Univ Amsterdam, Dept Med Oncol, Amsterdam UMC, Amsterdam, Netherlands
关键词
CD8-positive T cells; FOXP3; gastric cancer; invasive margin; prognostic marker; regulatory T cells; tumor-infiltrating lymphocytes; IMMUNE CELLS; SURVIVAL; IMMUNOSCORE; METASTASIS;
D O I
10.1016/j.modpat.2023.100218
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Tumor-infiltrating lymphocytes are associated with the survival of gastric cancer patients. T-cell densities in the tumor and its periphery were previously identified as prognostic T-cell markers for resectable gastric cancer. Immunohistochemistry for 5 T-cell markers, CD3, CD45RO, CD8, FOXP3, and granzyme B was performed on serial sections of N 1/4 251 surgical resection specimens of pa-tients treated with surgery only in the D1/D2 trial. Positive T cells were digitally quantified into tiles of 0.25 mm2 across 3 regions: the tumor center (TC), the inner invasive margin, and the outer invasive margin (OIM). A classification and regression tree model was employed to identify the optimal combination of median T-cell densities per region with cancer-specific survival (CSS) as the outcome. All statistical tests were 2-sided. CD8OIM was identified as the most dominant prognostic factor, followed by FOXP3TC, resulting in a decision tree containing 3 prognostically distinct sub-groups with high (Hi) or low (Lo) density of the markers: CD8OIMHi, CD8OIMLo/FOXP3TCHi, and CD8OIMLo/FOXP3TCLo. In a multivariable Cox regression analysis, which included pathological T and N stages, Lauren histologic types, EBV status, microsatellite instability, and type of surgery, the im-mune subgroups were independent predictors for CSS. CSS was lower for CD8OIMLo/FOXP3TCHi (HR: 5.02; 95% CI: 2.03-12.42) and for CD8OIMLo/FOXP3TCLo (HR: 7.99; 95% CI: 3.22-19.86), compared with CD8OIMHi (P < .0001). The location and density of both CD8 thorn and FOXP3 thorn T cells in resectable gastric cancer are independently associated with survival. The combination of CD8OIM and FOXP3TC T-cell densities is a promising stratification factor that should be validated in independent studies.& COPY; 2023 THE AUTHORS. Published by Elsevier Inc. on behalf of the United States & Canadian Academy of Pathology. This is an open access article under the CC BY license (http://creativecommons.org/ licenses/by/4.0/).
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页数:9
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