Prosigna DNA test avoids chemotherapy
Analysis based on 6 articles · First reported May 30, 2026 · Last updated Jun 02, 2026
The development of the Prosigna test by University College London is expected to significantly impact the healthcare and pharmaceutical industries by enabling more personalized breast cancer treatment. This could lead to reduced use of chemotherapy, affecting pharmaceutical companies producing chemotherapy drugs, while boosting demand for diagnostic tools like Prosigna. The United Kingdom — National Health Service and other health systems could see more efficient resource allocation.
Scientists, led by University College London, have developed a DNA test called Prosigna that can identify breast cancer patients who can safely avoid chemotherapy. An international study involving over 4,000 patients over 40 in countries including the United Kingdom, Norway, Sweden, Australia, New Zealand, and Thailand, found that more than two-thirds of participants could be treated with hormone therapy alone, sparing them from chemotherapy's severe side effects. The Prosigna test measures the activity of 50 genes to assess the risk of cancer recurrence. Patients with a low score, like Karen Bonham, showed a 93.7% five-year survival rate without chemotherapy, comparable to those who received it. Professor Rob Stein, the chief investigator, emphasized this as a step towards personalized treatment. The findings, described as 'practice-changing' by Professor David Miles, will be presented at the American Society of Clinical Oncology's annual meeting in Chicago, United States. This breakthrough could allow over 5,000 United Kingdom — National Health Service patients annually to avoid chemotherapy, leading to more efficient healthcare resource utilization.
Set up alerts, explore entity relationships, search across thousands of events, and build custom intelligence feeds.
Open Dashboard