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Prognostic significance of tumour stroma ratio in inflammatory breast cancer

Tumour stroma ratio (TSR) is emerging as an important prognostic indicator in cancer. We have previously shown TSR to be prognostic in oestrogen receptor positive breast cancer. Its role in inflammatory breast cancer, a rare but aggressive form of breast cancer, has not been identified. Here we aime...

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Detalles Bibliográficos
Autores principales: Downey, Candice L, Thygesen, Helene H, Sharma, Nisha, Shaaban, Abeer M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334919/
https://www.ncbi.nlm.nih.gov/pubmed/25713761
http://dx.doi.org/10.1186/s40064-015-0852-7
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author Downey, Candice L
Thygesen, Helene H
Sharma, Nisha
Shaaban, Abeer M
author_facet Downey, Candice L
Thygesen, Helene H
Sharma, Nisha
Shaaban, Abeer M
author_sort Downey, Candice L
collection PubMed
description Tumour stroma ratio (TSR) is emerging as an important prognostic indicator in cancer. We have previously shown TSR to be prognostic in oestrogen receptor positive breast cancer. Its role in inflammatory breast cancer, a rare but aggressive form of breast cancer, has not been identified. Here we aimed to determine the prognostic significance of TSR in a cohort of patients with inflammatory breast carcinoma. TSR was measured by point counting virtual H&E stained tissue sections in 45 inflammatory breast cancer cases. The whole tumour area was sampled. Optimum cut-offs to distinguish high and low TSR was determined by log-rank test. The relationship of TSR to overall survival and disease-free survival (DFS) was analysed alongside multivariate analysis. The optimal cut-offs between high and low TSR were determined to be 31% for OS and 46% for DFS. There was no significant difference in OS (p = 0.53) nor DFS (p = 0.66) between high and low TSR groups. Multivariate analysis did not demonstrate any new trends, within the limits of a small data sample. A significant correlation was found between pathological response to neoadjuvant chemotherapy and survival (p = 0.008). There is no evidence that TSR has prognostic significance in inflammatory breast cancer. When compared with published data in non-inflammatory breast carcinoma, this supports the view that differences in stromal biology exist between tumour types and highlights the importance of considering this when interpreting the prognostic value of TSR. However, these findings must be interpreted in the light of the small sample size.
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spelling pubmed-43349192015-02-24 Prognostic significance of tumour stroma ratio in inflammatory breast cancer Downey, Candice L Thygesen, Helene H Sharma, Nisha Shaaban, Abeer M Springerplus Research Tumour stroma ratio (TSR) is emerging as an important prognostic indicator in cancer. We have previously shown TSR to be prognostic in oestrogen receptor positive breast cancer. Its role in inflammatory breast cancer, a rare but aggressive form of breast cancer, has not been identified. Here we aimed to determine the prognostic significance of TSR in a cohort of patients with inflammatory breast carcinoma. TSR was measured by point counting virtual H&E stained tissue sections in 45 inflammatory breast cancer cases. The whole tumour area was sampled. Optimum cut-offs to distinguish high and low TSR was determined by log-rank test. The relationship of TSR to overall survival and disease-free survival (DFS) was analysed alongside multivariate analysis. The optimal cut-offs between high and low TSR were determined to be 31% for OS and 46% for DFS. There was no significant difference in OS (p = 0.53) nor DFS (p = 0.66) between high and low TSR groups. Multivariate analysis did not demonstrate any new trends, within the limits of a small data sample. A significant correlation was found between pathological response to neoadjuvant chemotherapy and survival (p = 0.008). There is no evidence that TSR has prognostic significance in inflammatory breast cancer. When compared with published data in non-inflammatory breast carcinoma, this supports the view that differences in stromal biology exist between tumour types and highlights the importance of considering this when interpreting the prognostic value of TSR. However, these findings must be interpreted in the light of the small sample size. Springer International Publishing 2015-02-10 /pmc/articles/PMC4334919/ /pubmed/25713761 http://dx.doi.org/10.1186/s40064-015-0852-7 Text en © Downey et al.; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Downey, Candice L
Thygesen, Helene H
Sharma, Nisha
Shaaban, Abeer M
Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title_full Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title_fullStr Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title_full_unstemmed Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title_short Prognostic significance of tumour stroma ratio in inflammatory breast cancer
title_sort prognostic significance of tumour stroma ratio in inflammatory breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334919/
https://www.ncbi.nlm.nih.gov/pubmed/25713761
http://dx.doi.org/10.1186/s40064-015-0852-7
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