Formula I Compound Combination for Cancer Treatment Efficacy

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Solution Overview

Problem

Current cancer treatments using anticancer medicaments often result in significant side effects and immunosuppression, which can lead to reduced efficacy and the development of cachexia, as these drugs also affect normal cells and induce immunosuppressive environments in tumor microenvironments.

Innovation Solution

The use of a compound of formula (I) or its pharmaceutically acceptable salt in combination with anticancer medicaments, such as topoisomerase inhibitors or platinum-based agents, to enhance cancer cell sensitivity, reduce side effects, and reverse immunosuppression, thereby attenuating cachexia symptoms.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If anticancer medicaments are used to kill cancer cells, then cancer cell growth is inhibited, but normal cells are also affected causing serious side effects

Engineering Contradiction:
Improvecancer cell killing efficacyVSAvoidside effects on normal cells
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent segments the therapeutic effect into two components: the anticancer medicament provides the primary cytotoxic effect, while the compound of formula (I) provides a protective effect on normal cells. This segmentation allows each component to perform its specialized function, achieving both cancer cell killing and normal cell protection simultaneously

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The compound of formula (I) acts as an intermediary substance that mediates between the anticancer medicament and normal cells. It interferes with the interaction between the medicament and normal cells, thereby reducing the harmful effects while maintaining the therapeutic effect on cancer cells

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If high dosage of anticancer medicaments is administered to ensure therapeutic effect, then cancer treatment efficacy is improved, but immunosuppression and cachexia symptoms worsen

Engineering Contradiction:
Improvetherapeutic effectVSAvoidimmunosuppression and cachexia
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent changes the dosage parameter of the anticancer medicament by introducing the compound of formula (I) as a co-administered substance. This allows the medicament to be administered at lower doses while maintaining therapeutic effect, thereby reducing immunosuppression and cachexia symptoms

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite therapeutic regimen combining the anticancer medicament with the compound of formula (I). This composite approach produces synergistic effects where the combination achieves better therapeutic outcomes at lower medicament doses, reducing harmful side effects

Inventive Principle:
Principle #40Composite materials

3Reliability

If anticancer medicaments are used to treat cancer, then tumor growth is controlled, but immunosuppressive environment is induced in tumor microenvironment

Engineering Contradiction:
Improvetumor growth controlVSAvoidimmunosuppressive microenvironment
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent converts the harmful immunosuppressive effect into a beneficial outcome by using the compound of formula (I) to counteract the immunosuppression induced by the anticancer medicament. This transforms the harmful immunosuppressive microenvironment into an immunocompetent environment that supports effective cancer treatment

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Data Source

PatentUS20230092846A1Combination for the treatment of cancer and application thereof
Publication Date: 2023.03.23 EVERFRONT BIOTECH
  • US20230092846A1 patent drawing
  • US20230092846A1 patent drawing
  • US20230092846A1 patent drawing

AI summary

A combination, comprising a first component and a second component; the first component is selected from a group composed of the following: the compound of formula (I), a pharmaceutically acceptable salt thereof, and a combination thereof, wherein A is a C1-C8 aliphatic hydrocarbon group optionally containing a carbonyl group as needed; X is H or OH; Y is O; and R1 is H or is not present, the condition being that when R1 is not present, Y and A bond to form a five-membered ring; and the second component is selected from a group composed of the following: a topoisomerase inhibitor, a microtubule assembly inhibitor, a platinum-based agent, an antimetabolite, and a combination thereof.