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A triple-negative breast cancer surrogate subtype classification that correlates with gene expression subtypes
Background This study developed a triple-negative breast cancer (TNBC) surrogate subtype classification that represents TNBC subtypes based on the Vanderbilt subtype classification. Methods Patients who underwent primary curative surgery for TNBC were included. Representative FFPE blocks were used f...
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Published in: | Breast cancer research and treatment 2022-02, Vol.191 (3), p.599-610 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
This study developed a triple-negative breast cancer (TNBC) surrogate subtype classification that represents TNBC subtypes based on the Vanderbilt subtype classification.
Methods
Patients who underwent primary curative surgery for TNBC were included. Representative FFPE blocks were used for gene expression analysis and tissue microarray construction for immunohistochemical (IHC) staining. The Vanderbilt subtypes were re-classified into four groups: basal-like (BL), mesenchymal-like (M), immunomodulatory (IM) and luminal androgen receptor (LAR) subtype. Classification and regression tree (CART) modeling was applied to develop a surrogate subtype classification.
Results
A total of 145 patients were included. The study cohort was allocated to the Vanderbilt 4 subtypes as LAR (
n
= 22, 15.2%), IM (
n
= 32, 22.1%), M (
n
= 38, 26.2%), BL (
n
= 25, 17.2%) and unclassified (
n
= 28, 19.3%). After excluding nine (6.2%) patients due to poor IHC staining quality, CART modeling was performed. TNBC surrogate subtypes were defined as follows: LAR subtype, androgen receptor Allred score 8; IM subtype, LAR-negative with a tumor-infiltrating lymphocyte (TIL) score > 70%; M subtype, LAR-negative with a TIL score |
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ISSN: | 0167-6806 1573-7217 |
DOI: | 10.1007/s10549-021-06437-8 |