Frame-Based Validation for Pathology Model Reliability

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Solution Overview

Problem

Current methods for evaluating cellular, molecular, and architectural features in histology samples are highly variable and lack standardization, making it difficult to determine the reliability of manual interpretations and validate algorithmic approaches for histological assessment.

Innovation Solution

A frame-based validation technique that involves accessing pathology images, generating distinct frames, receiving reference annotations from multiple users, processing these frames with a trained model to generate predictions, and validating the model's performance by determining the degree of association between annotations and predictions, using consensus scores and spatial proximity measures.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If manual scoring by pathologists is used to evaluate histological features, then human expertise and judgment are applied, but high variability and lack of standardization occur between and within pathologists

Engineering Contradiction:
Improvescoring consistencyVSAvoidreproducibility
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The pathology image is divided into multiple frames, and each frame is independently annotated by different pathologists. This segmentation allows for systematic collection of multiple annotations on the same region, enabling statistical analysis of variability and establishing consensus ground truth through aggregated annotations across multiple observers.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The system implements a feedback loop where model predictions are compared against consensus ground truth derived from multiple pathologist annotations. This feedback mechanism enables iterative model improvement and provides quantitative validation of algorithmic performance against standardized human expert consensus.

Inventive Principle:
Principle #23Feedback

2Reliability

If algorithmic approaches are used for histological assessment, then standardization and reproducibility improve, but validation against reliable ground truth becomes difficult due to pathologist variability

Engineering Contradiction:
ImprovereproducibilityVSAvoidground truth accuracy
Core Design Contradiction:
ReliabilityVSMeasurement precision

Solution Approach 1:

Multiple pathologist annotations on the same frame are merged to create a consensus ground truth. By combining multiple expert judgments through aggregation (e.g., majority voting or statistical consolidation), the system produces a more reliable and standardized reference that reduces individual observer variability and provides a robust benchmark for validating algorithmic approaches.

Inventive Principle:
Principle #5Merging (Combining)

3Measurement precision

If quantitative measures are implemented to reduce variability, then standardization improves, but the complexity of validation processes increases

Engineering Contradiction:
Improvescoring standardizationVSAvoidvalidation complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The system enables self-service validation where the framework automatically manages the complex processes of collecting multiple annotations, aggregating them into consensus ground truth, comparing model predictions against this ground truth, and generating validation metrics. This automated self-service approach handles the computational complexity while providing clear, standardized validation results without requiring manual orchestration of the validation process.

Inventive Principle:
Principle #25Self-service

Data Source

PatentUS11915823B1Systems and methods for frame-based validation
Publication Date: 2024.02.27 PATHAI INC
  • US11915823B1 patent drawing
  • US11915823B1 patent drawing
  • US11915823B1 patent drawing

AI summary

In some aspects, the described systems and methods provide for validating performance of a model trained on a plurality of annotated pathology images. A pathology image is accessed. Frames are generated using the pathology image. Each frame in the set includes a distinct portion of the pathology image. Reference annotations are received from one or more users. The reference annotations describe at least one of a plurality of tissue or cellular characteristic categories for one or more frames in the set. Each frame in the set is processed using the trained model to generate model predictions. The model predictions describe at least one of the tissue or cellular characteristic categories for the processed frame. Performance of the trained model is validated based on determining a degree of association between the reference annotations and the model predictions for each frame and/or across all frames in the set of frames.