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Multiplexed Fluorescent Immunohistochemical Staining, Imaging, and Analysis in Histological Samples of Lymphoma
Published on: January 9, 2019
Quantitative study of KI-67 antibody staining in non-Hodgkin's lymphomas using image analysis
Insights
Image analysis of KI-67 staining reliably quantifies proliferation in malignant lymphomas (ML). KI-67 area percentage correlates with cell counts, offering a faster alternative for grading these cancers.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Malignant lymphomas (ML) require accurate assessment of proliferative activity for grading and treatment.
- Quantifying proliferation is crucial for differentiating ML subtypes and predicting outcomes.
- Traditional manual cell counting can be time-consuming and subjective.
Purpose of the Study:
- To evaluate the reliability of image analysis for quantifying KI-67 proliferation in ML.
- To compare KI-67 area percentage with manual cell counting methods.
- To assess the utility of KI-67 area percentage in ML classification.
Main Methods:
- Analysis of KI-67 stained sections from 32 B-cell malignant lymphomas.
- Comparison of total KI-67 stained area percentage with the number of KI-67 positive cells.
- Statistical analysis using Pearson correlation and comparison of mean values between grades.
Main Results:
- A high correlation (r = .93) was observed between KI-67 area percentage and positive cell counts.
- Significant differences in KI-67 area percentage were found between low- and high-grade ML (Kiel classification).
- Follicular ML showed a wide range of KI-67 values, with follicular areas comparable to high-grade ML.
Conclusions:
- KI-67 area percentage determined by image analysis is a reliable alternative to manual cell counting for assessing ML proliferation.
- Image analysis provides quicker measurements over larger lymphomatous areas, increasing cell count accuracy.
- This method supports more efficient and accurate grading of malignant lymphomas.
Abstract:
In sections from 32 B malignant lymphomas (ML), the total KI-67 stained area was compared to the number of KI-67 positive cells in order to demonstrate the reliability of using image analysis to quantify the proliferative activity. The total KI-67 area percentage correlated highly with the number of KI-67 positive cellular profiles (r = .93). Significant differences were found between low- and high-grade ML according to the Kiel classification (mean values +/- SD, respectively, of 7.7 +/- 3.81% and 16.6 +/- 6.23%), and between low-, or intermediate- and high-grade ML only, according to the International Working Formulation. Within the Working Formulation, the statistical analysis grouped the diffuse large cell subtype of intermediate grade with the immunoblastic high-grade subtype. A wide range of KI-67 area percentage values was noted, particularly in follicular ML; for these follicular ML, considering follicular areas only, values were comparable to high-grade ML (14.8 +/- 6.60%). In conclusion, the KI-67 area percentage is a reliable alternative method to manual cell counting, and image analysis allows quicker measurements appropriate to large and strictly lymphomatous areas, using a greater number of cells than in manual cell counting.
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