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Histotype Px · Project

AI-Powered Digital Pathology to Reduce Unnecessary Chemotherapy in Colorectal Cancer Patients

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Imagine if doctors could tell exactly who needs chemotherapy and who doesn't just by looking at a digital photo of a tumor. Right now, many people get harsh treatments they don't actually need because the current tests aren't precise enough. This tool uses AI to scan those images and accurately predict if a patient will truly benefit from the medicine.

By the numbers
4 billion EUR
Global annual savings
250,000
Patients removed from unnecessary chemotherapy
>10
Hazard ratio for risk stratification
19 Billion
Economic burden of CRC in Europe
The business problem

What needed solving

Up to 90% of colorectal cancer patients receiving adjuvant chemotherapy may not benefit from it, leading to severe side effects and unnecessary healthcare spending.

The solution

What was built

Deep learning algorithms applied to cancer tissue whole slide images (WSI) to stratify patient risk.

Audience

Who needs this

Oncology clinicsDigital pathology laboratoriesHealth insurance companiesCancer research hospitals
Business applications

Who can put this to work

Healthcare Providers
enterprise
Target: Hospital Pathology Labs

If you are a hospital lab dealing with the high cost and risk of over-treating cancer patients — this project developed AI software that identifies low-risk patients in minutes. This can prevent up to 250,000 patients from receiving unnecessary chemotherapy.

Health Insurance
enterprise
Target: Medical Insurance Providers

If you are an insurer dealing with the high cost of cancer care and side-effect hospitalizations — this project developed a biomarker that could save 4 billion EUR globally every year by reducing unnecessary treatments.

Digital Health
mid-size
Target: Medical Imaging Software Vendors

If you are a software provider dealing with the need for more clinical utility in digital pathology — this project developed a deep learning algorithm for whole slide images that provides a hazard ratio >10 for risk stratification.

Frequently asked

Quick answers

How does this reduce healthcare costs?

Based on available project data, the tool can identify patients who do not need adjuvant chemotherapy, potentially saving 4 billion EUR globally every year.

Can this be scaled to existing labs?

Yes, the test can be run in local labs using existing digital pathology equipment and does not consume any tissue.

What is the intellectual property or licensing model?

Based on available project data, the technology is developed by DoMore Diagnostics AS, but specific licensing terms are not provided.

What is the clinical accuracy of the tool?

The biomarker provides risk stratification (low, intermediate, or high) with a hazard ratio >10.

What is the timeline for implementation?

The project period is from 2024-06-01 to 2026-05-31, focusing on broadening clinical validations to become the gold standard.

Consortium

Who built it

The project is led by a single partner, DoMore Diagnostics AS, a Norwegian SME. This 100% industry-led structure suggests a strong focus on commercialization and rapid market entry rather than academic exploration.

How to reach the team

Contact DoMore Diagnostics AS in Norway

Next steps

Talk to the team behind this work.

Contact us to explore licensing or partnership opportunities with DoMore Dx.

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