Blast Cell Image Classification Without CD Marker Panels

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Solution Overview

Problem

Current methods for classifying myeloid and lymphoid blast cells in leukemia are lengthy and require multiple stages of CD marker assessments, which are time-consuming and expensive.

Innovation Solution

A computer-implemented method using a parametric model classifier, such as a residual neural network, to differentiate between lymphoid and myeloid blast cells based on digital images of blood samples, reducing the need for extensive CD marker analysis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If multiple stages of CD marker assessment are used to classify blast cells, then classification accuracy is improved, but diagnosis time and cost increase significantly

Engineering Contradiction:
Improveclassification accuracyVSAvoiddiagnosis time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent segments the classification task into two distinct neural network models: a first model that identifies abnormal promyelocytes and other mononuclear blood cells, and a second model that specifically distinguishes myeloid from lymphoid lineage. This segmentation allows each model to specialize in a specific classification aspect, improving overall accuracy while enabling parallel processing that reduces total diagnosis time compared to sequential CD marker assessments.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent replaces the mechanical and chemical CD marker assessment process with a computational image analysis system using deep neural networks. Instead of physically isolating and chemically analyzing cell surface markers, the system uses digital imaging and automated neural network classification to identify and differentiate blast cells, dramatically reducing both time and cost while maintaining or improving classification accuracy.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Measurement precision

If multiple stages of CD marker assessment are used to classify blast cells, then classification accuracy is improved, but diagnostic cost increases

Engineering Contradiction:
Improveclassification accuracyVSAvoiddiagnostic cost
Core Design Contradiction:
Measurement precisionVSEase of manufacture

Solution Approach 1:

The patent uses digital copying of blood smear images to replace physical handling and multiple rounds of CD marker analysis. By creating and analyzing digital copies of cell images through neural networks, the system eliminates the need for repeated physical sample processing and chemical reagent consumption, significantly reducing diagnostic costs while maintaining classification accuracy.

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent employs a cost-effective digital imaging approach that replaces expensive and time-consuming CD marker panels. The neural network models process standard blood smear images without requiring additional expensive reagents or specialized equipment, making the diagnostic process more affordable and accessible.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

3Productivity

If a deep neural network classifier is used to identify abnormal promyelocytes, then identification speed is improved, but model complexity increases

Engineering Contradiction:
Improveidentification speedVSAvoidmodel complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent divides the complex classification problem into two separate neural network models with specific, focused functions. The first model handles identification of abnormal promyelocytes and mononuclear blood cells, while the second model specializes in lineage classification. This segmentation reduces the complexity of each individual model compared to a single comprehensive model, making them more manageable and interpretable while maintaining high identification speed.

Inventive Principle:
Principle #1Segmentation

Data Source

PatentEP4453894B1Blast cell classification
Publication Date: 2026.04.01 F HOFFMANN LA ROCHE & CO AG
  • EP4453894B1 patent drawingFigure 1
  • EP4453894B1 patent drawingFigure 2A
  • EP4453894B1 patent drawingFigure 2B

AI summary

A computer-implemented method of differentiating between lymphoid blast cells and myeloid blast cells comprises: receiving (S30) a digital image containing one or more blast cells; applying (S34) a parametric model classifier (412) to one or more portions of the digital image each containing a respective blast cell, the parametric model (416) configured to generate an output (S38) indicative of whether each blast cell is a lymphoid blast cell or a myeloid blast cell. Computer- implemented methods of training a parametric model (416) are also provided, as well as a clinical decision support system (400) relying on the computer-implemented method of classifying blast cells.