Virtual Staging Score for Biopsy-Free Cancer Detection

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Solution Overview

Problem

Current methods for detecting cancer, such as prostate cancer, face challenges including high false positive rates in PSA tests, difficulties in obtaining uniform tissue samples during biopsies, and reliance on invasive procedures that can cause complications, as well as inconclusive results due to sampling location issues, which are also applicable to other types of cancer like breast and lung cancer.

Innovation Solution

A biopsy-free method using a virtual staging score calculated from medical image data, including anatomical and functional imaging modalities like MRI and PET, combined with patient demographic and blood test data, to predict cancer staging scores non-invasively, eliminating the need for biopsies and potentially reducing unnecessary surgeries and complications.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If a biopsy is performed to detect cancer, then cancer detection can be performed, but the procedure is invasive and can cause bleeding, hemorrhage, and unnecessary complications

Engineering Contradiction:
Improvecancer detectionVSAvoidbleeding, hemorrhage, complications
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent creates a virtual copy of the biopsy process by using MRI imaging to generate a virtual Gleason score that replicates the diagnostic information normally obtained from tissue sampling. This virtual score model predicts cancer aggressiveness and staging without requiring actual tissue removal, thereby eliminating the harmful invasive effects while maintaining diagnostic reliability.

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent replaces the mechanical biopsy procedure with an imaging-based diagnostic system. Instead of physically removing tissue through a needle or scope, the system uses MRI scans to non-invasively capture cancer characteristics and compute a virtual Gleason score, substituting mechanical tissue sampling with electromagnetic imaging and computational analysis.

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

2Productivity

If a PSA blood test is used for initial detection, then cancer screening can be performed, but the test has a very high false positive rate leading to unnecessary biopsies

Engineering Contradiction:
Improvecancer screening efficiencyVSAvoidfalse positive rate
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent implements a feedback mechanism where the virtual Gleason score is calculated based on MRI imaging results and patient characteristics, providing a more accurate assessment that feeds back into the diagnostic decision-making process. This feedback loop allows clinicians to distinguish between true positives and false positives more effectively, reducing unnecessary biopsies while maintaining screening productivity.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The patent changes the diagnostic parameter from PSA blood test results to MRI-based virtual Gleason scores. This parameter transformation enables more precise cancer characterization by using imaging data that directly visualizes tumor morphology and characteristics, thereby improving reliability and reducing false positives while maintaining efficient screening capabilities.

Inventive Principle:
Principle #35Parameter changes

3Measurement precision

If a biopsy is performed to obtain tissue samples, then cancer diagnosis can be made, but it is challenging to acquire samples from all areas of the prostate, especially the peripheral zone

Engineering Contradiction:
Improvetissue sampling accuracyVSAvoidbiopsy performance difficulty
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent creates a comprehensive virtual map of the prostate using MRI imaging that replicates the complete tissue architecture without requiring physical sampling. The virtual Gleason score model processes this imaging data to assess cancer characteristics across the entire prostate volume, including difficult-to-reach peripheral zones, thereby achieving measurement precision equivalent to complete biopsies without the operational difficulties of performing such biopsies.

Inventive Principle:
Principle #26Copying

4Reliability

If Gleason scoring is performed based on tissue location, then cancer staging can be determined, but results are inconclusive when tissue is sampled from the wrong location

Engineering Contradiction:
Improvecancer staging accuracyVSAvoidinconclusive results
Core Design Contradiction:
ReliabilityVSLoss of information

Solution Approach 1:

The patent creates a complete virtual replica of the prostate anatomy and cancer lesions through MRI imaging, eliminating the information loss that occurs when biopsies miss the correct location. The virtual Gleason score model processes this comprehensive imaging data to accurately determine cancer staging and aggressiveness, ensuring reliable results without the inconclusiveness that arises from sampling errors in traditional biopsies.

Inventive Principle:
Principle #26Copying

Data Source

PatentUS10424411B2Biopsy-free detection and staging of cancer using a virtual staging score
Publication Date: 2019.09.24 SIEMENS HEALTHINEERS AG
  • US10424411B2 patent drawing
  • US10424411B2 patent drawing
  • US10424411B2 patent drawing

AI summary

A method for predicting a cancer staging score from medical image data includes receiving patient data for a plurality of patients, where patient data for each of the plurality of patients includes one or more of an image volume of a suspected tumor in an organ, blood test data, demographic data, and ground truth tumor staging scores for the suspected tumor in the organ, extracting features from the patient data, and using the features extracted from the patient data to train a classifier to predict a cancer staging score for a new patient from one or more of an image volume of a suspected tumor in the organ, patient blood test data and patient demographic data of that new patient.