Gene Expression Profiles Predict Ovarian Cancer Chemotherapy Response

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Solution Overview

Problem

Current methods lack effective predictive biomarkers to differentiate between ovarian cancer patients who will respond well to platinum-paclitaxel or platinum-only chemotherapy, leading to suboptimal treatment outcomes.

Innovation Solution

Identification of specific gene expression profiles, including biomarkers such as ICAM1, TUBB2A, GLDC, PLAU, AURKA, NEAT1, MXRA5, GSN, and MUC16 for platinum-paclitaxel chemotherapy, and FCGBP, TFPI, NUAK1, LRRC17, FLRT2, IL12A, HSPA2, CDC20, FOXM1, and MAP4K2 for platinum-only chemotherapy, to predict treatment response.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If standard chemotherapy treatment is administered to ovarian cancer patients, then treatment coverage is provided, but treatment efficacy cannot be predicted and outcomes remain suboptimal

Engineering Contradiction:
Improvetreatment response predictionVSAvoidpatient response information
Core Design Contradiction:
ReliabilityVSLoss of information

Solution Approach 1:

The patent applies preliminary action by identifying and measuring biomarker expression levels in tumor tissue before initiating chemotherapy treatment. This allows the treatment approach to be selected or adjusted in advance based on predicted response, rather than observing outcomes after treatment begins. The biomarkers (such as those listed in Tables 6-7) are assessed pre-treatment to predict whether a patient will respond well to platinum-paclitaxel or platinum-only chemotherapy.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent uses biomarkers as intermediary elements that mediate between the patient's tumor biology and the chemotherapy treatment decision. These biomarkers serve as measurable indicators that translate complex tumor characteristics into actionable predictive information, enabling clinicians to select the most appropriate chemotherapy regimen before treatment begins.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Adaptability or versatility

If platinum-paclitaxel or platinum-only chemotherapy is selected without predictive biomarkers, then treatment can be administered, but treatment selection is based on convention rather than patient-specific response likelihood

Engineering Contradiction:
Improvepersonalized treatment strategyVSAvoidresponse prediction accuracy
Core Design Contradiction:
Adaptability or versatilityVSMeasurement precision

Solution Approach 1:

The patent applies parameter changes by measuring specific biomarker expression levels (such as ICAM1, TUBB2A, GLDC, PLAU, AURKA, NEAT1, MXRA5, GSN, and MUC16 for platinum-paclitaxel; or FCGBP, TFPI, NUAK1, LRRC17, FLRT2, IL12A, HSPA2, CDC20, FOXM1, and MAP4K2 for platinum-only) to determine the most appropriate chemotherapy regimen. This transforms treatment selection from a conventional approach to a personalized one based on measurable biological parameters.

Inventive Principle:
Principle #35Parameter changes

3Productivity

If no predictive biomarkers are used, then treatment decisions can be made quickly, but one-third of patients experience disease progression or recurrence after initial treatment

Engineering Contradiction:
Improvetreatment decision speedVSAvoidtreatment outcome reliability
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent enables preliminary assessment of treatment likelihood through biomarker measurement before chemotherapy initiation. This allows treatment decisions to be made with predictive information, improving outcome reliability while maintaining efficient decision-making through objective biomarker criteria rather than prolonged observation or trial-and-error approaches.

Inventive Principle:
Principle #10Preliminary action

Data Source

PatentUS20250290156A1Evaluating ovarian cancer chemotherapy response using gene expression data and machine learning
Publication Date: 2025.09.18 GEORGE MASON UNIVERSITY
  • US20250290156A1 patent drawing
  • US20250290156A1 patent drawing
  • US20250290156A1 patent drawing

AI summary

The present disclosure generally relates to gene expression profiling of tissue samples obtained from ovarian cancer patients who are candidates for chemotherapy treatment. More specifically, the disclosure provides methods based on characterization of gene expression which allow a physician to predict whether a patient is likely to respond well to treatment with a chemotherapeutic reagent.