AzTrials
AzTrials

Neuroendocrine Tumor of PancreasPRIMENCT05037461

Precision Radiotherapy Using MR-linac for Pancreatic Neuroendocrine Tumours in MEN1 Patients

A study testing High-dose-high precision MR-guided radiotherapy in people with Neuroendocrine Tumor of Pancreas and Multiple Endocrine Neoplasia Type 1, run by J.M. de Laat at 1 site in Netherlands.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
Search all trials

Trial summary

Patients with the Multiple Endocrine Neoplasia type 1 (MEN1) syndrome are genetically predisposed for developping multiple pancreatic neuro-endocrine tumours (pNET). The management of small (pNET) in both MEN1 and sporadic cases, pose a major clinical challenge. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
High-dose-high precision MR-guided radiotherapy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteNetherlands
Study dates
27 Jun 2022to Jul 2027
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
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Suspected malignant pNET as per the tumour board assessment, including the criteria:
  • pNET lesions of more than 3 cm in size
  • rapid growth of pNET lesions with more than 4mm per year
  • Symptomatic pNET because of hormone production, with the exception of gastrinomas which are located in the submucosa of the duodenum
  • concurrent treatment with a somatostatin analog
  • concurrent treatment with chemotherapy
Show all 12Show fewer
  • peptide receptor radionuclide therapy in the past 12 months
  • history of radiotherapy in the upper abdominal region
  • MRI contraindications as per usual clinical care, such as claustrophobia and metal or electronic implants not compatible with MRI.
  • Pregnancy
  • (Other) metastatic disease
  • WHO performance score 3-4

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • UMC Utrecht

    Utrecht, Utrecht, 3584 CX

Other trials in Netherlands

About this study

Official title: PRIME Study: Precision Radiotherapy Using MR-linac for Pancreatic Neuroendocrine Tumours in MEN1 Patients

Patients with the Multiple Endocrine Neoplasia type 1 (MEN1) syndrome are genetically predisposed for developping multiple pancreatic neuro-endocrine tumours (pNET). The management of small (pNET) in both MEN1 and sporadic cases, pose a major clinical challenge. At present, pancreatic surgery is the only curative treatment but it is associated with high morbidity. To reduce the morbidity ascosiated with surgery and thereby potentially improve quality of life for MEN1 patients introduction of less invasive techniques for treatment of pNET is important. High-dose-high precision MR-guided radiotherapy (MRgRT) holds promise as a new less invasive treatment option for pNET. The aim of this study is to assess efficiacy and safety of MRgRT for treatment of pNET in MEN1 patients.

Read the detailed description

Background Patients with the Multiple Endocrine Neoplasia type 1 (MEN1) syndrome are genetically predisposed for developping multiple pancreatic neuro-endocrine tumours (pNET), with a cumulative pNET incidence of over 80% at an age of 80 years. In MEN1 patients, metastatic pNET is the primary cause of premature death.

The management of small (pNET) in both MEN1 and sporadic cases, pose a major clinical challenge. At present, pancreatic surgery is the only curative treatment. Since surgery is associated with significant short- and long-term morbidity the management of small pNET depends on carefully outweighing the risk of liver metastasis leading to premature death and the morbidity of pancreatic surgery. Guidelines advocate that for tumours smaller than 2 cm an intensive watchful waiting strategy seems to be safe. However, although most pNETs remain indolent for years, many lesions eventually progress and metastasize. To prevent the development of metastases for growing tumours or tumours above 2 cm a surgical resection is advised. Due to the high incidence of pNET in the MEN1 population many MEN1 patients receive surgery for pNET in their lifespan and cope with the morbidity of pancreatic surgery. To reduce the morbidity ascosiated with surgery and thereby potentially improve quality of life for MEN1 patients introduction of less invasive techniques for treatment of pNET is important.

High-dose-high precision MR-guided radiotherapy (MRgRT) holds promise as a new less invasive treatment option for pNET. With MRgRT accurate and precise delivery of high irradiation dose levels to the pNET is possible, while monitoring the tumor with MR imaging. The UMC Utrecht has pioneered the development of this technology, and gained experience with MRgRT treatments for patients with pancreatic adenocarcinoma and other upper abdominal malignancies.

Aim Aim of this project is to assess the safety and efficacy of high-dose-high precision MRgRT for pNET in a cohort of MEN1 patients that will require surgery in the near future.

Methods Efficacy and safety of MRgRT will be explored in a prospective cohort study of MEN1 patients with pNET, the Precision Radiotherapy using MRLInac for Pancreatic Neuroendocrine Tumours in MEN1 patients (PRIME)study. The PRIME study is a single arm interventional cohort study, recruiting 20 MEN1 patients enrolled in the Dutch MEN1 Study Groups (DMSG) longitudinal cohort. Eligible patients are patients with pNET surpassing 2.0 cm, and patients with a growing pNET measuring between 1.0- 2.0 cm. Patients who give informed consent will receive MRgRT with a minimum dose to the tumour bed of 40 Gy in 5 fractions delivered within 2 weeks. The primary outcome will be the change in maximum diameter of pNET at follow-up MRI scan at 12 months after diagnosis. Secondary outcome parameters include incidence of surgical resection following MRgRT, toxicity of radiotherapy, quality of life, endocrine and exocrine pancreatic functioning, metastases free survival, overall survival and tumour characteristics on follow-up MRI.

Being tested
High-dose-high precision MR-guided radiotherapy
Medical subject headings
Adenoma, Islet Cell, Multiple Endocrine Neoplasia Type 1

What participants receive

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

  • High-dose-high precision MR-guided radiotherapyRadiation

    MR-guided radiotherapy as described in the group information

Study groups in NCT05037461
Study groupRoleWhat they receive
High-dose-high precision MR-guided radiotherapyExperimentalRadiotherapy for pancreatic NET will be delivered in an image-guided, hypofractionated scheme of 5 fractions of 8 Gy, prescribed to 95% of the planning target volume (PTV). Treatment is delivered on alternate days 2 or 3 times a week with a maximum overall treatment time of 14 days on the 1.5T MR-Linac (Elekta Unity MR-Linac). The Gross Tumor Volume (GTV) is defines as the pNET visible on pre-treatment CT and MRI scan. No clinical target volume (CTV) is used. The PTV is made by adding a 3mm margin to the GTV. The treatment plan is a 9-14 field intensity modulated radiotherapy (IMRT) plan with dose prescribed to 95% of the PTV. While respecting the dose constraints to adjacent tissues
Receives: Radiation: High-dose-high precision MR-guided radiotherapy

What is being measured

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

  1. Change in tumor size

    Change in maximal diameter of pNET measured at follow-up MRI

    Measured: 12 months

Secondary outcomes (16)
  1. Tumour progression

    Number of patients with signs of growth or metastasis at follow-up

    Measured: 12 months

  2. Pancreatic surgery

    Number of patients that require surgical treatment following MRgRT

    Measured: 12 months

  3. Toxicity of radiotherapy

    Toxicity of radiotherapy graded according to Common Terminology Criteria for Adverse Events v4.0 scale

    Measured: 12 months

  4. Health-related quality of life by SF-36

    Short Form Health Survey 36 items

    Measured: 6 months, 12 months

  5. Health-related quality of life by Eq5D

    EuroQol 5D instrument

    Measured: 6 months, 12 months

  6. Health-related quality of life by PROMIS-29

    PROMIS 29 profile

    Measured: 6 months, 12 months

  7. fasting glucose

    fasting glucose in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  8. blood cell count,

    blood cell count in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  9. serum iron

    serum iron v

    Measured: 12 month in evaluation of endocrine and exocrine pancreatic function

  10. vitamin B12

    vitamin B12 in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  11. folate

    folate in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  12. faecal fat test

    faecal fat test in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  13. faecal trypsin

    faecal trypsin in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  14. faecal elastase

    faecal elastase in evaluation of endocrine and exocrine pancreatic function

    Measured: 12 months

  15. metastases free survival

    Measured at follow-up imaging

    Measured: 12 months

  16. overall survival

    survival

    Measured: 12 months

Timeline

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

  1. First posted8 Sep 2021
  2. Study start27 Jun 2022
  3. Primary completionJul 2027 (estimated)
  4. Study completionJul 2027 (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
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
Prospective cohort study
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05037461
Sponsor's protocol ID
NL77809.041.21
Acronym
PRIME
Status last verified
Sep 2026
First submitted
25 Aug 2021
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data will be placed in a repository and made available upon reasonable request, as stated in our data management plan.

Questions about this trial

What is this clinical trial studying?

A study testing High-dose-high precision MR-guided radiotherapy in people with Neuroendocrine Tumor of Pancreas and Multiple Endocrine Neoplasia Type 1, run by J.M. de Laat at 1 site in Netherlands.

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 0 inclusion and 12 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: under way, not looking for participants, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. 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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in tumor size (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 9 Sep 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in