Completed Digestion, Kidneys & Other Organs Cancer

Development of a test to guide breast cancer treatment

In plain English

AI plain-English summary

A new blood test could tell thousands of breast cancer patients each year whether chemotherapy will actually help them after surgery. The DDRD Breast Assay, developed by Almac Diagnostics, identifies which patients with early-stage, node-negative breast cancer are likely to benefit from standard chemotherapy and which are not. Patients who test “positive” are roughly four times less likely to relapse than those who test “negative”, giving clinicians and patients concrete information to guide treatment decisions. Currently, many women receive chemotherapy that offers them little or no benefit, exposing them to harsh side effects unnecessarily. This test aims to spare those patients from toxic treatments while ensuring that those who truly need chemotherapy receive it. The project will validate the assay for CE marking, then launch it in the UK private health market and establish a registry. The team will also gather evidence on clinical utility and cost-effectiveness to support a submission to NICE, with the goal of making the test available on the NHS. If approved, the test could become a routine part of post-surgery care, quietly reshaping how breast cancer treatment is personalised across the UK.

View original technical description
The DDRD Breast Assay has been developed by Almac Diagnostics to help clinicians and patients decide on whether the use of chemotherapy may be an appropriate approach following surgery for early stage node negative breast cancer patients. Patients who are called “positive” are approximately 4 times less likely to have a relapse compared to patients who are called “negative” by the test. This type of information is extremely valuable to both clinicians and patients as it allows a much more informed decision to be made on whether an individual patient is likely to benefit from standard of care chemotherapy. During the course of this project the DDRD Breast Assay will undergo further analytical and clinically validation to gain CE marking. On approval from the MHRA, it will be launched in the UK private health market and a DDRD Breast Registry established. Suitable clinical validation, analytical validation, clinical utility and cost effectiveness evidence will be gathered to support a submission to NICE with a view to launching this test in the Public UK health market.

View the original record at the funder ↗

Related Research

Grants with similar aims, by meaning.

Accelerating the diagnosis, management, and support of people diagnosed with cancer
RanDX for predicting breast cancer recurrence and metastasis
Digistain - Breast Cancer Companion Diagnostic for over-prescribed chemotherapy
Digistain mid-IR Cancer detection technology; a calibration and validation study.
DEployment of an AI-based solution for supporting Breast cancer diagnosis and assessment of Overall cost-effectiveness, Reliability, Accuracy and impact on Healthcare (DEBORAH)

Original classification

Small Business Research Initiative

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.