Lymphoma Treatment Prediction via Gene Expression Clustering

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Solution Overview

Problem

Current methods for treating lymphoma, particularly diffuse large B-cell lymphoma (DLBCL), lack specificity and effectiveness due to the clinical and biological heterogeneity of the disease, leading to variable patient responses to standard treatments like R-CHOP.

Innovation Solution

A method for predicting the responsiveness of lymphoma patients to cancer treatment by clustering reference lymphoma patients into subgroups based on gene expression levels and determining the subgroup of the patient, thereby predicting treatment responsiveness and potentially tailoring treatment approaches.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If standard chemotherapy treatments like R-CHOP are administered to all lymphoma patients, then treatment coverage is comprehensive, but treatment effectiveness varies due to disease heterogeneity

Engineering Contradiction:
Improvetreatment effectivenessVSAvoidtreatment personalization
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent segments lymphoma patients into distinct molecular subtypes (GCB-DLBCL, ABC-DLBCL, PMBL) based on gene expression profiling. This segmentation allows identification of specific patient groups with different treatment responses, enabling personalized treatment selection rather than uniform standard therapy for all patients.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent applies local quality by tailoring treatment approaches to specific molecular subtypes. Different chemotherapy regimens and targeted therapies are recommended for different subtypes (e.g., NF-κB pathway inhibitors for ABC-DLBCL), making the treatment quality specific to each patient's molecular characteristics rather than applying a one-size-fits-all approach.

Inventive Principle:
Principle #3Local quality

2Adaptability or versatility

If gene expression profiling is performed to identify molecular subtypes, then treatment personalization is improved, but diagnostic complexity and cost increase

Engineering Contradiction:
Improvetreatment personalizationVSAvoiddiagnostic complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent changes the diagnostic parameter from traditional clinical classification to molecular gene expression profiling. By measuring specific gene expression levels (e.g., BCL6, MUM1, CD10, BCL2) and comparing them against established thresholds, the system transforms complex biological data into discrete molecular subtype classifications that guide treatment decisions.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces molecular subtyping as an intermediary between diagnosis and treatment selection. The gene expression profile serves as a mediator that translates complex disease heterogeneity into actionable treatment recommendations, bridging the gap between clinical presentation and personalized therapy selection.

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentUS20250188545A1Methods for predicting responsiveness of lymphoma to drug and methods for treating lymphoma
Publication Date: 2025.06.12 CELGENE CORP
  • US20250188545A1 patent drawing
  • US20250188545A1 patent drawing
  • US20250188545A1 patent drawing

AI summary

Provided herein are methods of predicting the responsiveness of a lymphoma patient to a cancer treatment comprising clustering patients into subgroups of patients using gene expression levels. Also provided herein are methods of treating a lymphoma patient based on predicting the responsiveness of the lymphoma patient to a cancer treatment.