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The prognostic value of the tumour-stroma ratio in primary operable invasive cancer of the breast: a validation study.

Toni Roeke ,
Marcelo Sobral-Leite ,
Tim J A Dekker ,
Jelle Wesseling ,
Vincent T H B M Smit ,
Rob A E M Tollenaar ,
Marjanka K Schmidt ,
Wilma E Mesker

Abstract

METHODS

A retrospective cohort study was performed on women diagnosed and treated for primarily operable invasive breast cancer in the period from 1 January 1990 till 31 December 1999. Tumour-stroma ratio was estimated by microscopic evaluation of haematoxylin and eosin tumour slides. Two independent observers (k = 0.68) performed tumour-stroma ratio evaluation in a significant part of the cohort. The prognostic potential with respect to overall, recurrence-free and distant metastasis-free survival was evaluated.

CONCLUSION

Tumour-stroma ratio is an independent risk factor for worse overall, distant metastasis-free and recurrence-free survival in primarily operable breast cancer. However, detailed prospective studies with respect to tumour-stroma ratio are necessary to gain more insight in its prognostic potential in clinical practice.

RESULTS

A total of n = 737 women were evaluated. Median follow-up time was 11.5 years. High stromal content was an independent prognosticator for worse overall (hazard ratio 1.56, p = 0.002, 95% confidence interval 1.18-2.05), distant metastasis-free (hazard ratio 1.52, p = 0.008, 95% confidence interval 1.12-2.06) and recurrence-free survival (hazard ratio 1.35, p = 0.046, 95% confidence interval 1.01-1.81). In subgroups of hormone receptor-positive and lymph node-negative cases, high stromal content was also an independent prognosticator for worse outcome.

PURPOSE

The primary aim of the current study is to validate the prognostic relevance of the relative amount of tumour-associated stroma, the tumour-stroma ratio, in a large cohort of primary operable breast cancer patients.

More about this publication

Breast cancer research and treatment

Volume 166
Issue nr. 2
Pages 435-445
Publication date 01-11-2017

Full text links

Publisher website (DOI) 10.1007/s10549-017-4445-8
Europe PubMed Central 28795248
Pubmed 28795248

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