Abstract
KI-67 is a marker for cell proliferation which binds a nuclear antigen and is thus a prime antibody in immunohistochemistry. Scoring methodologies derived from KI-67 immunostaining have shown promise as predictors of lethality in a range of cancers [1]. The most common scoring method is the labelling index, a ratio of KI-67 positive cells to the entire population [1]. Manual calculation of a labelling index can be a time-consuming process for pathologists, who count cells in a bright field. Automated scoring algorithms and programs have been written to generate labelling indices, but they are nonspecific with respect to cell type and most often skew results by including stromal cells in the index. This problem is particularly relevant in breast cancer, where tumors are often located in a field of fibroadipose tissue. We have adapted algorithms for immunostain scoring and tested 2 stromal cell filtration algorithms which remove these cells based on their elongated nuclear morphology.
Highlights
KI-67 is a marker for cell proliferation which binds a nuclear antigen and is a prime antibody in immunohistochemistry
Manual calculation of a labelling index can be a timeconsuming process for pathologists, who count cells in a bright field
This problem is relevant in breast cancer, where tumors are often located in a field of fibroadipose tissue
Summary
KI-67 is a marker for cell proliferation which binds a nuclear antigen and is a prime antibody in immunohistochemistry. The most common scoring method is the labelling index, a ratio of KI-67 positive cells to the entire population [1]. Automated scoring algorithms and programs have been written to generate labelling indices, but they are nonspecific with respect to cell type and most often skew results by including stromal cells in the index. This problem is relevant in breast cancer, where tumors are often located in a field of fibroadipose tissue. We have adapted algorithms for immunostain scoring and tested 2 stromal cell filtration algorithms which remove these cells based on their elongated nuclear morphology
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