Study of PSMA PET imaging versus standard imaging to guide radiation therapy in patients with intermediate or high-risk prostate cancer

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What is this study about?

This study focuses on patients with intermediate-risk or high-risk prostate cancer who are planned to receive radiotherapy. The research evaluates the effectiveness of using a special imaging technique called PSMA PET (Prostate-Specific Membrane Antigen Positron Emission Tomography) to guide radiation treatment planning. The study uses Locametz, which contains the active substance gozetotide, as an imaging agent that is given through an intravenous injection.

The purpose of the study is to compare the outcomes of radiation treatment when planned using PSMA PET imaging versus standard imaging methods. The study involves two groups of patients – one group will receive radiation therapy planned using conventional imaging, while the other group will have their treatment planned using PSMA PET scans. Each participant will receive a single dose of the imaging agent before their radiation treatment planning.

During the study, patients will be monitored for several years to track their response to treatment and any changes in their cancer status. The monitoring includes regular check-ups and various tests to assess how well the treatment is working. The study medication (Locametz) is already approved for use in medical imaging and will be given as a single dose of up to 259 MBq (a measure of radioactivity).

1 Initial qualification

You will be evaluated for participation if you are a male, 18 years or older, with confirmed prostate cancer

Your cancer must be classified as intermediate- to high-risk, which means having at least one of these factors: PSA>10ng/mL, advanced tumor stage, or specific risk scores

You need to be physically able to perform daily activities without assistance (ECOG status 0-1)

2 Study group assignment

You will be randomly assigned to one of two groups

One group will receive standard imaging before radiation therapy

The other group will receive PSMA PET imaging (a special type of scan) before radiation therapy

3 Imaging procedure

If assigned to the PSMA PET group, you will receive Locametz, a diagnostic medicine given through an intravenous injection

The imaging results will be used to plan your radiation treatment

4 Radiation therapy

You will undergo radiation therapy based on your imaging results

The treatment plan will be customized according to your specific situation

5 Follow-up period

Your progress will be monitored through regular check-ups

Blood tests will be performed to measure PSA levels (a protein that can indicate cancer activity)

Additional imaging may be performed if needed

The study will continue until 2033

6 Safety considerations

You must use appropriate contraception during the study

After receiving the study medication, you should avoid sperm donation for 24 hours

Any side effects will be monitored and documented throughout the study

Who Can Join the Study?

  • Must be male
  • Must be 18 years or older
  • Must agree not to donate sperm for 24 hours after receiving study treatment
  • Must sign an informed consent form showing understanding of the study purpose and procedures
  • Must have confirmed prostate adenocarcinoma (a type of prostate cancer) through tissue examination
  • Must have intermediate to high-risk disease with at least one of these conditions:
    • PSA blood test above 10 ng/mL
    • Cancer stage 2b or higher
    • Gleason score 7 or higher (a measure of cancer aggressiveness)
    • Decipher Score 0.45 or higher (a genetic test that measures cancer risk)
  • Must be willing to undergo radiation therapy
  • Must be willing to have PSMA PET scan results used in radiation therapy planning if assigned to that study group (PSMA PET is a special type of imaging scan)
  • Must have good physical function status (ECOG grade 0 or 1, meaning able to carry out all or most daily activities)
  • Must agree to use condoms during sexual activity while receiving study treatment and for 24 hours afterward

Who Cannot Join the Study?

  • Previous treatment with radiation therapy (a treatment that uses high doses of radiation to destroy cancer cells) to the prostate or pelvic area
  • Previous surgery of the prostate
  • Known allergies or hypersensitivity to substances used in PET imaging (a type of medical scan that helps detect cancer)
  • Presence of metal implants or devices that would interfere with imaging procedures
  • Unable to lie flat for the required imaging procedures
  • Any condition that makes it impossible to deliver radiation therapy safely
  • Participation in other clinical trials that could interfere with this study
  • Female patients (study is only for male patients)
  • Age under 18 years
  • Presence of cancer that has spread beyond the prostate to other parts of the body
  • Serious medical conditions that could interfere with study participation or patient safety
  • Unable to provide informed consent

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

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Other Sites

Site Name City Country Status
Uulgodcgkvxvbzmmsdrbe Esqqd Axd Essen Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Germany Germany
Not yet recruiting
01.08.2025

Trial locations

Investigated drugs:

Based on the provided trial information, the main imaging therapies involved are:

PSMA PET (Prostate-Specific Membrane Antigen Positron Emission Tomography) is an advanced imaging technique that uses a special radioactive tracer to create detailed pictures of prostate cancer cells throughout the body. This imaging method is particularly effective at detecting prostate cancer, even in its early stages.

Standard-of-care imaging includes conventional imaging techniques typically used for prostate cancer detection and monitoring. These may include CT scans (Computed Tomography) and bone scans, which are traditional methods used to evaluate prostate cancer spread and plan radiation treatment.

Radiation Therapy (RT) is used as the main treatment in this trial, with its planning and delivery being guided by either PSMA PET or standard imaging results. This therapy uses high-energy radiation to target and destroy cancer cells in the prostate.

Investigated diseases:

Prostate Cancer – A disease that develops in the prostate gland, which is part of the male reproductive system. It typically begins when normal prostate cells start to grow uncontrollably. The cancer usually develops slowly and initially stays within the prostate gland, where it may not cause serious harm. As the disease progresses, cancer cells may spread beyond the prostate into surrounding tissues. In its early stages, prostate cancer often causes no noticeable symptoms. The condition is more common in older men and tends to grow more slowly compared to many other types of cancer.

Trial ID:
2023-506032-33-00
Protocol code:
P4RTY
Trial Phase:
Therapeutic confirmatory (Phase III)

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