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Standardized Assessment of the Tumor-Stroma Ratio in Colorectal Cancer: Interobserver Validation and Reproducibility of a Potential Prognostic Factor
Author(s) -
Ricella Souza da Silva,
Eduardo Queiroga,
Alexandre Rolim da Paz,
Fabiana F P Neves,
Karin Soares Cunha,
Eliane Pedra Dias
Publication year - 2021
Publication title -
clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.242
H-Index - 10
ISSN - 2632-010X
DOI - 10.1177/2632010x21989686
Subject(s) - stromal cell , concordance , stroma , colorectal cancer , medicine , kappa , reproducibility , tumor grade , pathology , oncology , adenocarcinoma , cancer , stromal tumor , immunohistochemistry , chemistry , linguistics , philosophy , chromatography
The tumor stroma plays a relevant role in the initiation and evolution of solid tumors. Tumor-stroma ratio (TSR) is a histological feature that expresses the proportion of the stromal component that surrounds cancer cells. In different studies, the TSR represents a potential prognostic factor: a rich stroma in tumor tissue can promote invasion and aggressiveness. The aim of this study was to evaluate the reproducibility and determine the interobserver agreement in the TSR score. The stromal estimate was evaluated in patients diagnosed with colorectal adenocarcinoma (CRA), who underwent surgical resection. We also evaluated age, gender, and other anatomopathological features. Tumor-stroma ratio was calculated based on the slide used in routine diagnostic pathology to determine the T-status. Stromal percentages were separated into 2 categories: ⩽50%—low stroma and >50%—high stroma. The interobserver agreement in the TSR scoring was evaluated among 4 pathologists at different stages of professional experience, using 2 different ways to learn the scoring system. In total, 98 patients were included in this study; 54.1% were male, with a mean age of 61.9 years. Localized disease was diagnosed in 60.2% of patients. Stromal-poor CRA was predominant. The concordance between the TSR percentages of the 4 pathologists was substantial (Kappa > 0.6). There was greater agreement among pathologists for stromal-poor tumors. Substantial agreement and high reproducibility were observed in the determination of TSR score. The TSR score is feasible, suggesting that the presented methodology can be used to facilitate the determination of the stromal proportion of potential prognostic factor.

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