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The prognostic value of the tumor-stroma ratio is most discriminative in patients with grade III or triple-negative breast cancer.

Kiki M H Vangangelt ,
Andrew R Green ,
Isabelle M F Heemskerk ,
Danielle Cohen ,
Gabi W van Pelt ,
Marcelo Sobral-Leite ,
Marjanka K Schmidt ,
Hein Putter ,
Emad A Rakha ,
Rob A E M Tollenaar ,
Wilma E Mesker

Abstract

The tumor-stroma ratio (TSR) was evaluated as a promising parameter for breast cancer prognostication in clinically relevant subgroups of patients. The TSR was assessed on hematoxylin and eosin-stained tissue slides of 1,794 breast cancer patients from the Nottingham City Hospital. An independent second cohort of 737 patients from the Netherlands Cancer Institute to Antoni van Leeuwenhoek was used for evaluation. In the Nottingham Breast Cancer series, the TSR was an independent prognostic parameter for recurrence-free survival (RFS; HR 1.35, 95% CI 1.10-1.66, p = 0.004). The interaction term was statistically significant for grade and triple-negative status. Multivariate Cox regression analysis showed a more pronounced effect of the TSR for RFS in grade III tumors (HR 1.89, 95% CI 1.43-2.51, p < 0.001) and triple-negative tumors (HR 1.86, 95% CI 1.10-3.14, p = 0.020). Comparable hazard ratios and confidence intervals were observed for grade and triple-negative status in the ONCOPOOL study. The prognostic value of TSR was not modified by age, tumor size, histology, estrogen receptor status, progesterone receptor status, human epidermal growth factor receptor 2 status or lymph node status. In conclusion, patients with a stroma-high tumor had a worse prognosis compared to patients with a stroma-low tumor. The prognostic value of the TSR is most discriminative in grade III tumors and triple-negative tumors. The TSR was not modified by other clinically relevant parameters making it a potential factor to be included for improved risk stratification.

More about this publication

International journal of cancer

Volume 146
Issue nr. 8
Pages 2296-2304
Publication date 15-04-2020

Full text links

Publisher website (DOI) 10.1002/ijc.32857
Europe PubMed Central 31901133
Pubmed 31901133

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