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Prostate CancerIP9-ATLASNCT06280781

Imperial Prostate 9 - ATLAS (Approaches To Long-Term Active Surveillance)

A study testing MRI Scans in people with Prostate Cancer, run by Imperial College London at 12 sites in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this intervention study is for patients on active surveillance for prostate cancer, to demonstrate that use of regular MRI scans is better able to detect cancer progression over 5 years compared to the current NICE defined strategy. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Prostate Cancer
What is being tested?
MRI Scans
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,263 participants
Where
12 sitesUnited Kingdom
Study dates
24 May 2024to Jun 2032
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 years or above (no upper limit)
  • Patients with a prostate (either cis-male gender or trans-female gender with no prior androgen deprivation hormone use at all).
  • Diagnostic bi-parametric or multiparametric MRI
  • Diagnostic systematic biopsy +/- targeted biopsy
  • A histological diagnosis of localised prostate cancer
  • Patient chosen active surveillance

Who cannot join

  • On active surveillance for greater than 9 months prior to screening date.
  • Contraindication to MRI or gadolinium contrast
  • Previous hip replacement to both hips
  • Contraindication to performing a biopsy guided by a transrectal ultrasound probe

Trial locations and contacts

12 sites in 1 country. Contact the study team or a site near you to ask about taking part.

12 sites in 1 country

United Kingdom12 sites, 12 recruiting
  • Heatherwood Hospital

    Ascot, Berkshire, SL5 7GB

    Lauren Barnett, lauren.barnett6@nhs.net

    Nishant Bedi

    Recruiting
  • Bradford Royal Infirmary

    Bradford

    Imran Hamid, 07778 954483, imran.hamid@bthft.nhs.uk

    Rohit Chahal

    Recruiting
  • St Peter's Hospital

    Chertsey

    Keshnie Govender, 01932726851, keshnie.govender@nhs.net

    Nimalan Arumainayagam

    Recruiting
  • Darent Valley Hospital

    Dartford, Kent, DA2 8DA

    Charlotte Kamundi, charlotte.kamundi1@nhs.net

    Sanjeev Madaan

    Recruiting
  • Charing Cross Hospital

    London, W6 8RF

    Archana Gopalakrishnan, archana.gopalakrishnan@imperial.ac.uk

    Hashim Ahmed

    Recruiting
  • Kings College London

    London

    Sahin Emer, 0 203 299 6860, sahin.emer@nhs.net

    Nicholas Raison

    Recruiting
  • West Middlesex Hospital

    London

    Metod Oblak, 07766064813, metod.oblak@nhs.net

    Mathias Winkler

    Recruiting
  • Freeman Hospital

    Newcastle upon Tyne

    Jade Whitehead, 0191 2137322, jade.whitehead2@nhs.net

    Rajan Veeratterapillay

    Recruiting
  • Glan Clywd Hospital

    Rhyl

    Sharon Harland, +44 3000 844543, Sharon.Harland@wales.nhs.uk

    Kingsley Ekwueme

    Recruiting
  • Northern Lincolnshire and Goole NHS Foundation Trust

    Scunthorpe

    Dorota Potoczna, 03033 305867, dorota.potoczna@nhs.net

    Mark Rogers

    Recruiting
  • Southampton University Hospital

    Southampton

    Nikki Carney, Nikki.Carney@uhs.nhs.uk

    Aneta Zahorska, Aneta.Zahorska@uhs.nhs.uk

    Recruiting
  • North Cumbria

    Whitehaven

    Rachel Mutch, 07811714656, Rachel.mutch@ncic.nhs.uk

    Yannick Yangue

    Recruiting

Other trials in United Kingdom

About this study

Official title: A Randomised Controlled Trial of Regular MRI Scans Compared to Standard Care in Patients With Prostate Cancer Managed Using Active Surveillance

The goal of this intervention study is for patients on active surveillance for prostate cancer, to demonstrate that use of regular MRI scans is better able to detect cancer progression over 5 years compared to the current NICE defined strategy.

Research Question P - In patients who are on active surveillance for low to medium risk prostate cancer, I - is the use of regular MRI scans C - compared to current NICE defined standard of care, O - better at detecting cancer progression with less cost to the NHS (fewer PSA tests, biopsies and clinic visits)?

Patients will be allocated in a 1.1 ratio to either MRI scans or the current NICE defined standard. Randomisation will be blocked (random block size) and stratified by MRI visibility of lesions (3 categories [ no visible lesion, diffuse changes, discrete visible lesion]), cancer Grade Group (GG1, GG2) and time since diagnosis. This study will not be blinded to patients or physicians.

Read the detailed description

What is the problem being addressed?

Of 50,000 newly diagnosed patients with prostate cancer every year, about 7,600 choose active surveillance rather than immediate surgery or radiotherapy. Most have low risk whilst 20-30% have medium risk prostate cancer. This is because low and medium risk prostate cancers grow slowly. As a result, immediate treatment does not improve cancer-specific survival over 10 years but can cause high rates of urinary, sexual and bowel side-effects.

Although these cancers are slow growing, 25-34% will progress to higher risk over 5 years and need treatment later. Whilst there is no evidence that delayed detection of progression has an impact on survival, a recent systematic review has shown detrimental effects on other aspects of cancer control. For instance, in the largest RCT comparing active surveillance to immediate surgery or radiotherapy, 2-3 times as many patients had disease progression and cancer spread to other parts of the body in the active surveillance arm. So, active surveillance needs to be improved. NICE currently advise that active surveillance should involve 3-6 monthly prostate specific antigen (PSA) blood tests and rectal examinations. They advise an MRI and biopsy at 12 months. After one year, 3-6 monthly PSA and rectal examinations are recommended and further biopsy if the PSA starts to rise or if the rectal exam detects a prostate nodule.

This is problematic for 3 reasons:

First, PSA and rectal examination changes are inaccurate in detecting progression. As a result, some centres do regular biopsies every 1-2 years; this is borne out by a 48 physician survey (Jan 2022). However, biopsies alone are also inaccurate as they are ultrasound-guided; the operator can see the prostate but not areas suspicious for cancer progression.

Second, biopsies have side-effects such as infection, bleeding and pain; when these occur, patients are less likely to agree to further biopsies. Biopsies cost £488 and lead to significant NHS resource use. Regular and repeat biopsies can also cause prostate scarring making surgery more difficult if it is needed later.

Third, 10-43% of patients often decide to have treatment even if the cancer has not progressed. This is because of anxiety about living with cancer, or because of the biopsy and burden of tests. Some studies have shown other psychological impacts such as sub-clinical depression, illness uncertainty and hopelessness.

The Investigators propose using regular MRI scans in active surveillance to detect progression. The team led the pivotal UK studies which changed recommendations for MRI in diagnosing prostate cancer. Subsequently, The Investigators and others have shown that regular prostate MRI scans with targeted biopsies to areas of suspicion are accurate in ruling-out and detecting progression. To change NHS practice, an RCT is needed to compare regular MRI scans to current NICE defined standard of care in patients who choose active surveillance following an MRI-directed biopsy at time of diagnosis.

The studies proposal was positively reviewed by the NCRI Prostate Proposal Guidance panel (7/2/2022).

Why is this research important?

  1. The regular use of MRI in active surveillance will lead to greater confidence in active surveillance for patients with low and medium risk prostate cancer. This is because such a strategy is likely to detect cancer progression earlier with fewer invasive biopsies. In previous studies, 1 of 672 patients chose treatment during surveillance due to anxiety.
  2. An additional ~2000 patients with medium risk cancer could be managed with active surveillance in future.
  3. Fewer NHS resources for clinic follow-ups, PSA tests and biopsies.

Of 5 research priorities that NICE have identified for prostate cancer, two relate to improving active surveillance. Similarly, the James Lind Alliance has 3 research priorities to improve active surveillance.

Research Question P - In patients who are on active surveillance for low to medium risk prostate cancer, I - is the use of regular MRI scans C - compared to current NICE defined standard of care, O - better at detecting cancer progression with less cost to the NHS (fewer PSA tests, biopsies and clinic visits)?

  1. Aims and Objectives

Primary Objective

In patients on active surveillance for prostate cancer, to demonstrate that use of regular MRI scans is better able to detect cancer progression over 5 years compared to the current NICE defined strategy.

Difference between current and planned care pathways

Current (NICE defined active surveillance):

PSA 3 monthly in year 1 and then 6 monthly with rectal exam annually. MRI will be carried out at 12 months (if not had one at diagnosis). A biopsy will be required if indicated due to changes in rectal exam or PSA.

Planned (Regular MRI based active surveillance):

Patients with a visible lesion or medium risk cancer will have PSA 6 monthly and MRI annually. All other patients will undergo PSA 6 monthly and MRI in years 1, 3 and 5. In all patients, a targeted biopsy will be carried out if the MRI PRECISE score is >/=4.

Conditions
Prostate Cancer
Being tested
MRI Scans
Medical subject headings
Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MRI ScansDiagnostic test

    The regular use of MRI in active surveillance will lead to greater confidence in active surveillance for patients with low and medium risk prostate cancer. This is because such a strategy is likely to detect cancer progression earlier with fewer invasive biopsies. Those patients randomised to the intervention arm will have additional MRI scans. These will be non-contrast so there is no risk from having repeated 1-2 yearly injections of gadolinium contrast. Patients with contraindications to MRI will not be taking part in the study so will not be exposed to an unnecessary MRI.

    Patients with a visible lesion or medium risk cancer will have PSA 6 monthly and MRI annually. All other patients will undergo PSA 6 monthly and MRI in years 1, 3 and 5. In all patients, a targeted biopsy will be carried out if the MRI PRECISE score is >/=4.

Study groups in NCT06280781
Study groupRoleWhat they receive
Standard care (Control) ArmNo interventionPSA 3 monthly in year 1 and then 6 monthly with rectal exam annually if clinically indicated. MRI will be carried out at 12 months (if not had one at diagnosis). If a diagnostic MRI was carried out, a 12 month MRI scan will not be required. A biopsy will be required if indicated due to changes in rectal exam or PSA. Follow-up for 5 years.
Intervention ArmExperimentalPatients with a visible lesion or medium risk cancer will have PSA 6 monthly and MRI scans annually. As per international PIRADS committee guidance the surveillance MRIs will be biparametric MRI scans which last approximately 15 minutes and exclude gadolinium contrast injection. All other patients will undergo PSA 6 monthly and MRI in years 1, 3 and 5. In all patients, a targeted biopsy will be carried out if the MRI PRECISE score is >/=4.
Receives: Diagnostic Test: MRI Scans

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Biopsy

    Progression in each group defined as higher risk cancer on biopsy (Grade Group >/=3)

    Prostate cancer progression rates and time to progression in each randomised arm defined on,

    • biopsy: grade progression to Grade Group 3 or greater or detection on biopsy of intraductal cancer or lymphovascular invasion. Many of our clinicians would include patients on active surveillance with cribriform pattern on Grade Group so this is not a factor for progression.

    Measured: 5 Years

  2. Staging

    Progression in each group defined as higher risk cancer on higher stage (>/=T3 or >/=N or >/=M1) over 5 years.

    Prostate cancer progression rates and time to progression in each randomised arm defined on,

    • staging: cancer has spread to surrounding tissues (extracapsular), lymph node involvement or distant body parts as demonstrated on cross-sectional imaging including MRI, CT, bone-scan or PET scans as deemed appropriate by the local multidisciplinary cancer team.

    Measured: 5 Years

Secondary outcomes (8)
  1. Cost-effectiveness

    Cost-effectiveness of revising the prostate cancer active surveillance protocol to incorporate regular surveillance MRI within the NHS (QALYs questionnaire).

    Measured: 5 Years

  2. Biopsy Measurement

    Biopsy would be recommended when there is a change on the MRI or if there is a consistent rise in PSA over 3 readings that is concerning for progression even if the MRI shows no change and other factors such as infection or prostatitis have been ruled out.

    Measured: 5 years

  3. MRI & biopsy-related adverse events

    Patients will be asked to self-report pain and discomfort (referred to as pain hereafter) immediately after and seven days after biopsy on a 4-point Likert-type scale as none, mild, moderate, or severe. Specific related complications such as fever, flu-like shivers, pain, haematuria, haematochezia, and haemoejaculate will be self-reported at 35 to 90 days after prostate biopsy as absent or present following biopsy on a purpose designed questionnaire. For each symptom, patients will be asked to score the degree of "problem" as none, minor, moderate, or major. This will be used to derive a binary outcome for each symptom (present/moderate/severe problem vs. absent /minor problem).

    Measured: 5 Years

  4. Treatment

    Patients treatment options for progressive disease will be collected through multidisciplinary team (MDT) outcomes in the clinical records and clinic letters or entries by clinicians in the health records. Such options depending on cancer risk include; active surveillance, focal therapy, radical surgery or radiotherapy (with some men started on androgen deprivation therapy).

    Measured: 5 Years

  5. Compliance

    Compliance measured as proportion having each test (PSA, rectal exam, MRI) at each allocated timepoint and proportion agreeing to a biopsy when clinically recommended

    Measured: 5 Years

  6. EPIC Questionnaires

    Annual changes in patient reported outcome measure (PROMS) using validated questionnaires, compared to baseline, to measure impact on urinary, erectile and bowel function (EPIC).

    Measured: 5 years

  7. HADS Questionnaires

    Annual changes in patient reported outcome measure (PROMS) using validated questionnaires, compared to baseline, to measure impact on cancer-related anxiety (HADS)

    Measured: 5 Years

  8. EQ-5D-5L Questionnaires

    Annual changes in patient reported outcome measure (PROMS) using validated questionnaires, compared to baseline, to measure impact on overall health-related quality of life (EQ-5D-5L)

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2024
  2. Study start24 May 2024
  3. Primary completionJun 2029 (estimated)
  4. Study completionJun 2032 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Factorial
Model description
Current (NICE defined active surveillance): PSA 3 monthly in year 1 and then 6 monthly with rectal exam annually. MRI will be carried out at 12 months (if not had one at diagnosis). A biopsy will be required if indicated due to changes in rectal exam or PSA. Planned (Regular MRI based active surveillance): Patients with a visible lesion or medium risk cancer will have PSA 6 monthly and MRI annually. All other patients will undergo PSA 6 monthly and MRI in years 1, 3 and 5. In all patients, a targeted biopsy will be carried out if the MRI PRECISE score is \>/=4.
Masking
None (open label)
Enrolment
1,263 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06280781
Sponsor's protocol ID
22CX7971
Other IDs
NIHR152027
Acronym
IP9-ATLAS
Status last verified
Mar 2026
First submitted
25 Jan 2024
Last updated
30 Mar 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Gopalakrishnan A, Light A, Mayor N, Cullen E, Rawlins F, Dalton R, Tanaka MB, Connor MJ, De Dios CC, Fiorentino F, Ali A, Akinyemi I, Klimowska-Nassar N, Sasikaran T, Monk R, Baker G, Andrews M, Sculpher M, Rothery C, Barrett T, Mangar S, Freeman A, Winkler M, Heer R, Shah TT, Sokhi HK, Giganti F, Punwani S, Emberton M, Ahmed HU. The Imperial Prostate 9 - Approaches To Long-term Active Surveillance: Regular MRI scans versus standard of care (IP9-ATLAS) randomised controlled trial. Contemp Clin Trials. 2026 Jun;165:108308. doi: 10.1016/j.cct.2026.108308. Epub 2026 Apr 15.

    PubMed 41990428

Questions about this trial

What is this clinical trial studying?

A study testing MRI Scans in people with Prostate Cancer, run by Imperial College London at 12 sites in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 12 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Hashim Ahmed (+44 (0)20 7594 1660, hashim.ahmed@imperial.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Biopsy (time frame: 5 Years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06280781, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2026.

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