MicroRNA Panel for Colorectal Cancer Recurrence Prediction

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Solution Overview

Problem

Current diagnostic methods for colorectal cancer are inadequate in identifying patients at high risk for recurrence, leading to potential missed opportunities for early intervention and improved outcomes.

Innovation Solution

The use of a combination of microRNAs (miR-15a, miR-103, miR-148a, miR-320a, and miR-451) in circulating biological materials to predict recurrence risk, allowing for tailored monitoring and treatment strategies post-surgery.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If surgery alone is used as standard care for early stage CRC patients, then treatment simplicity is maintained, but recurrence risk identification capability deteriorates

Engineering Contradiction:
Improvetreatment simplicityVSAvoidrecurrence risk identification capability
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The patent applies preliminary action by performing microRNA analysis on circulating biological materials before making treatment decisions. This allows recurrence risk to be identified in advance, enabling proactive selection of patients who would benefit from adjuvant therapy rather than relying on surgery alone.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent introduces microRNA expression profiles as an intermediary diagnostic tool between surgery and recurrence monitoring. These molecular markers serve as mediators that provide information about recurrence risk, allowing clinicians to make informed decisions about additional therapy without directly observing cancer recurrence.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If microRNA analysis is performed to identify high-risk patients, then recurrence risk identification capability is improved, but diagnostic complexity increases

Engineering Contradiction:
Improverecurrence risk identification capabilityVSAvoiddiagnostic complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent applies segmentation by analyzing specific individual microRNAs (miR-15a, miR-103, miR-148a, miR-320a, miR-451) rather than attempting to measure all possible molecular markers. This segmented approach to biomarker analysis reduces diagnostic complexity while maintaining accurate recurrence risk identification capability.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent utilizes parameter changes by measuring expression levels of specific microRNAs in circulating biological materials. This shifts the diagnostic parameter from anatomical or clinical observations to molecular expression levels, enabling more precise recurrence risk assessment through quantifiable molecular data.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If adjuvant therapy is provided to high-risk patients, then survival benefit is improved, but treatment intensity increases

Engineering Contradiction:
Improvesurvival benefitVSAvoidtreatment intensity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies local quality by providing adjuvant therapy selectively to specific patient subgroups identified as high-risk through microRNA analysis, rather than applying intensive treatment to all patients. This localized approach ensures that increased treatment intensity is applied only where it provides survival benefit, optimizing the balance between reliability and treatment burden.

Inventive Principle:
Principle #3Local quality

Data Source

PatentUS10351913B2Compositions and methods for identification of relapse risk and treatment in patients with colorectal cancer
Publication Date: 2019.07.16 GEORGETOWN UNIV
  • US10351913B2 patent drawing
  • US10351913B2 patent drawing
  • US10351913B2 patent drawing

AI summary

In certain aspects, the disclosure relates to methods of predicting recurrence of colorectal cancer by using a combination of microRNAs in the circulation, wherein the microRNAs are selected from the group consisting of miR-15a, miR-103, miR-148a, miR-320a, miR-451 and miR-596. In other aspects, the disclosure relates to methods of treating colorectal cancer by administering a therapeutic agent after determining an increased risk of recurrence.