ArticleDiagnostic pathology2018
Does heterogeneity matter in the estimation of tumour budding and tumour stroma ratio in colon cancer?
Article in Diagnostic pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
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Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it.
- A scoping review of TSR analysis in colorectal cancer: implications for automated solutions.Oncology reviews · 2025Pooled it
- The Glasgow Microenvironment Score: an exemplar of contemporary biomarker evolution in colorectal cancer.The journal of pathology. Clinical research · 2024Review
- The Prognostic Impact of Tumor Border Configuration, Tumor Budding and Tumor Stroma Ratio in Colorectal Carcinoma.Turk patoloji dergisi · 2023Article
- Tumor Stroma Ratio and Its Significance in Locally Advanced Colorectal Cancer.Current oncology (Toronto, Ont.) · 2022Review
- Tumour-stroma ratio outperforms tumour budding as biomarker in colon cancer: a cohort study.International journal of colorectal disease · 2021Article
- Low Tumor-to-Stroma Ratio Reflects Protective Role of Stroma against Prostate Cancer Progression.Journal of personalized medicine · 2021Article
- Prognostic Significance of Lacunarity in Preoperative Biopsy of Colorectal Cancer.Pathology oncology research : POR · 2020Article
- Tumor proportion in colon cancer: results from a semiautomatic image analysis approach.Virchows Archiv : an international journal of pathology · 2020Article
- Grainyhead-Like Genes Family May Act as Novel Biomarkers in Colon Cancer.OncoTargets and therapy · 2020Article
- The prognostic value of tumour stroma ratio and tumour budding in stage II colon cancer. A nationwide population-based study.International journal of colorectal disease · 2018Article
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7 authors.
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Abstract
backgroundTumour budding (TB) and Tumour Stroma Ratio (TSR) may be rewarding in the treatment stratification of patients with stage II colon cancer. However, lack of standardization may exclude these parameters from being used in a clinical setting. The purpose of this methodologic study was to compare stereology with semi-quantitative estimations of TSR, to investigate the intra-tumoural heterogeneity of TB and TSR, and to assess the intra- and inter-observer agreement.
methodsThree paraffin embedded tumour blocks, one of them representing the deepest invasive front, were selected from each of 43 patients treated for stage II colon cancer. TSR was estimated in H&E sections semi-quantitatively using conventional microscopy, and stereologically on scanned slides, using the newCAST stereology platform. TB was scored across 10 high power fields at the invasive front in cytokeratin AE1/AE3 stained sections.
resultsSubjective, semi-quantitative estimates of TSR significantly correlated to the stereological estimates, with the best correlation found for sections with the deepest invasive tumour penetration (σ = 0.621, p < 0.001). Inter-observer agreement was moderate to substantial for both TB (Κappa = 0.46-0.73) and TSR (Κappa = 0.70-0.75). The Intraclass correlation coefficient (ICC) for TSR varied from 0.322 based on stereological hotspot estimation to 0.648 for the semi-quantitative evaluation. For TB, ICC varied from 0.646 based on continuous data to 0.698 based on categorical data (cut-off: 10 buds). Thus, the intra-tumoural heterogeneity for both TB and the semi-quantitative estimation of TSR was low.
conclusionWe recommend using only one tissue section representing the deepest invasive tumour area for estimation of TSR. For TB we recommend using one tissue section; however due to low representation of high-budding tumours, results must be considered with caution.
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