East Genomics

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Test kits for ctDNA testing

ctDNA testing is now available as standard of care for non-small cell lung cancer, ESR1 in breast cancer, and Cancer of Unknown Primary (CUP). Testing requires NHS Trusts to procure their own sample collection kits, which are then sent to certain regional Genomic Medicine Services (GMSs) for testing. In the East region, ctDNA testing will be delivered via the North Thames Genomic Medicine Service.

Non-urgent advice: NEW July 2026; ctDNA testing for Cancer of Unknown Primary

From 16 July 2026, patients with CUP can be referred for circulating tumour DNA (ctDNA) testing via the NHS Genomic Test Directory. Already used in non-small cell lung cancer (NSCLC) and ESR1 in breast cancer, ctDNA testing uses a simple blood test to detect tumour DNA circulating in the bloodstream. For patients with CUP, this can help:

  • Identify the likely tissue of origin
  • Detect clinically actionable genomic alterations
  • Support diagnosis, treatment decisions and access to clinical trials

For the East region testing will be routed through the North Thames Genomic Medicine Service.

You can view a webinar held on 7 July below. You can also:

ctDNA for CUP: Webinar

Link: https://www.youtube.com/watch?v=c5HDA6aeZcI

Ordering ctDNA blood collection kits

Those in the East Genomics region should order tests and send samples to the North Thames GMS.

We have worked with Trusts across our region to support the funding and procurement of appropriate sampling kits. If you are unsure how to access testing, please contact:

Ordering kits

Contact Marsden360@rmh.nhs.uk

Laboratory address

Clinical Genomics

The Centre for Molecular Pathology

The Royal Marsden NHS Foundation Trust

Cotswold Road

Sutton Surrey

SM2 5PT

ctDNA test request form (North Thames GMS)

Benefits of ctDNA testing

Detection of ctDNA can be a fast and effective way to detect cancer and demand for these tests is expected to continue to grow.

Key benefits of testing include:

  • Earlier access to targeted treatments and reduced need for repeated invasive procedures
  • System-wide cost savings from diagnostic procedures for patients with failed genomic tests
  • Cost savings from avoided mistreatment and associated consequences
  • Improved quality of life for patients accessing treatment sooner
  • Reduced cancer waiting times