Prognostic significance of tumour stroma ratio in inflammatory breast cancer

被引:20
|
作者
Downey, Candice L. [1 ]
Thygesen, Helene H. [2 ]
Sharma, Nisha [1 ]
Shaaban, Abeer M. [3 ,4 ]
机构
[1] St James Univ Hosp, Leeds LS9 7TF, W Yorkshire, England
[2] Univ Leeds, St Jamess Univ Hosp, Leeds Inst Canc & Pathol, Leeds LS9 7TF, W Yorkshire, England
[3] Queen Elizabeth Hosp, Dept Cellular Pathol, Birmingham B15 2TW, W Midlands, England
[4] Univ Birmingham, Birmingham B15 2TW, W Midlands, England
来源
SPRINGERPLUS | 2015年 / 4卷
关键词
Breast cancer; Inflammatory; Stroma; Tumour-stroma ratio; Prognosis; INDEPENDENT PREDICTOR; SURVIVAL; CARCINOMA;
D O I
10.1186/s40064-015-0852-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:4
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