At a glance
- What the study gets you
- Health checks and monitoring — no treatment given
- Type of study
- Observational (no treatment given)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Matched Tumour and Blood Sample - Research Pathway (other), Matched Tumour and Blood Sample - NHS GMS pathway (other)
- How long the study runs
- Study runs about 87 months (dates as stated)
- About the drug or intervention
- Matched Tumour and Blood Sample - Research Pathway — other: For patient's undergoing surgery fresh tissue will be collected from the initial surgery and frozen until shipment to the Oxford BRAIN MATRIX Lab. · Matched Tumour and Blood Sample - NHS GMS pathway — other: Tessa Jowell BRAIN MATRIX centres in England can submit matched tissue and blood samples for Whole Genome Sequencing through the standard of care NHS Genomic Medicine Service pathway via their Genomic Laboratory Hub.
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Observing health over time
- Ages
- 16 Years and over
- Who
- All
- Number of participants
- 1,000
- Started
- 2020-11-24
- Last checked
- 2026-04
Plain English Summary
What is this study?
- • Testing a new treatment for glioma
- • Clinical study - 1,000 participants
- • The main aim of the Tessa Jowell BRAIN MATRIX - Platform Study is to more precisely determine the exact type of tumour patients have by developing the essential infrastructure to provide rapid and accurate molecular diagnosis
Who can take part?
- • Ages 16 Years and over
- • Diagnosed with glioma
Where?
- • Birmingham - Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust
- • Cambridge - Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust
- • Cardiff - Velindre Cancer Centre, Velindre University NHS Trust
- • Edinburgh - NHS Lothian
- • +10 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The main aim of the Tessa Jowell BRAIN MATRIX - Platform Study is to more precisely determine the exact type of tumour patients have by developing the essential infrastructure to provide rapid and accurate molecular diagnosis. A large network of clinical hubs across the United Kingdom, with expertise in managing patients with brain tumours, will be developed. Once established this infrastructure will facilitate the rapid introduction of clinical trials testing targeted therapies tailored to the genetic changes of an individual's tumour.
More detail
Gliomas, a type of brain tumour, are the most common primary tumour of the central nervous system (CNS) and in 2016 there were 5250 deaths from brain tumours in the UK. However, brain tumours are a challenging disease to treat. The tumour's location within the brain and its tendency to grow into nearby brain tissue often make it very difficult to remove the tumour completely with surgery. There is also difficulty in delivering drugs in adequate amounts to the tumour due to the natural defences of the brain. Brain tumours arise due to changes in the DNA and other molecules in cells of the brain. Different types of gliomas can have different changes and these can be used to determine a precise 'molecular diagnosis'. The ultimate goal for the Tessa Jowell BRAIN MATRIX is to learn how to use these molecular changes to more precisely determine what exact type of tumour patients have, and to identify, decide and test whether specific 'targeted' treatments could improve the survival and/or quality of life of patients with brain tumours. Tessa Jowell BRAIN MATRIX is a programme of work, the principal purpose of which is to improve the knowledge of, and treatment for, glioma. The programme will include a Platform Study and subsequent interventional clinical trials. The Tessa Jowell BRAIN MATRIX Platform Study forms the backbone of this programme. In the Platform Study, the aim is to develop the infrastructure to provide rapid and accurate molecular diagnosis and the infrastructure to deliver clinical trials of new therapies in the future, thereby improving clinical outcomes in brain tumours. The researchers aim to recruit 1,000 patients to the study. As gliomas occur at all ages and their specific subtype is hard to predict pre-operatively, the patient population eligible for the study is broad. A large network of clinical hubs across the UK, with expertise in managing patients with brain tumours, will be developed. Once established this infrastructure will facilitate the rapid introduction of clinical trials testing targeted therapies tailored to the genetic changes of an individual's tumour. Eligible patients will either have had, or be about to have, surgery for their tumour. As part of this study, tumour removed during the operation will be analysed to look for specific molecular changes. As with normal standard care, the tumour will be analysed by a local pathologist. A small part will be sent for review by experts and advanced molecular analysis will be undertaken to get a detailed understanding of the DNA/molecular changes within the patient's tumour. These results will be fed back to the patient's treating doctor. It is intended that this will occur within 28 days; however, it may be longer while the study becomes fully operational. If samples are available from a patient's previous surgery to their tumour, these may also be analysed. Similarly, if available, other relevant samples such as cerebrospinal fluid, collected as part of their care, may also be analysed. In addition, as technologies and analyses improve the understanding of brain tumours, the researchers may find important results at a later date. These will be fed back to the patient's doctor. Patients will also be asked to give a blood sample, which will also be analysed to look at the molecular features, including of their DNA. This is required to identify what 'new' changes have occurred in the patient's tumour. Following surgery, patients will continue with other treatment(s) as directed by their doctor. Treatment generally involves radiotherapy and chemotherapy. As is standard practice, patients will be closely monitored for signs of disease progression and the effects of the treatment given. As part of this study, information on patients' treatments and disease will be collected. Images from brain scans patients undergo, along with relevant clinical information, will also be sent to and stored by the University of Edinburgh, and where appropriate, undergo expert review by a panel of radiologists with expertise in brain tumours. If patients have further surgery, some of the tissue removed may also be analysed.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 16 Years and over
- Who can join: All genders
What the study is looking for
- ✓Newly diagnosed suspected WHO Grade 2-4 glioma, (as evidenced radiologically) AND suitable for a diagnostic or...
- ✓Patients with progression with known WHO Grade 2-4 glioma (those with available frozen tumour will be prioritised...
- ✓Valid written agreement to take part for the study.
Who cannot take part
- ✗Primary spinal cord tumours
- ✗Active treatment of other cancer
- ✗safety concern to MRI
- ✗Patients without the usual treatment imaging available
See the full criteria
Where Is This Study? (14 UK sites)
Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust
Birmingham B15 2TH, United Kingdom
Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust
Cambridge CB2 0QQ, United Kingdom
Velindre Cancer Centre, Velindre University NHS Trust
Cardiff CF14 2TL, United Kingdom
NHS Lothian
Edinburgh EH4 2XU, United Kingdom
Queen Elizabeth Unviersity Hospital, NHS Greater Glasgow and Clyde Health Board
Glasgow G51 4TF, United Kingdom
St James's University Hospital, Leeds Teaching Hospitals NHS Trust
Leeds LS9 7TF, United Kingdom
The Walton Centre, The Walton Centre NHS Foundation Trust
Liverpool L9 7LJ, United Kingdom
King's College Hospital, King's College Hospital NHS Foundation Trust
London SE5 9RS, United Kingdom
Charing Cross Hospital, Imperial College Healthcare NHS Trust
London W6 8RF, United Kingdom
The Christie Hospital, The Christie NHS Foundation Trust
Manchester M20 4BX, United Kingdom
Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust
Manchester M6 8HD, United Kingdom
Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust
Newcastle upon Tyne NE7 7DN, United Kingdom
Queen's Medical Centre, Nottingham University Hospitals NHS Trust
Nottingham NG7 2UH, United Kingdom
Churchill Hospital, Oxford University Hospitals NHS Foundation Trust
Oxford OX3 9DU, United Kingdom
How to Get in Touch
Rhys Mant
Sponsor contactCONTACT
Joshua Savage
Sponsor contactCONTACT
