Prostate Cancer
Conditions
Keywords
prostate cancer, biochemical recurrence, 18F-PET imaging
Brief summary
Prostate cancer is the most frequently occurring male cancer in Belgium. Patients who have been treated for prostate cancer, i.e. by surgery and/or radiotherapy, in a substantial degree suffer from a tumor recurrence, often diagnosed by an increase in serum tumor marker PSA (prostate specific antigen) within the first few years. In these patients with evidence of a tumor recurrence after primary treatment, it is important to most exactly define the location(s) of tumor, to guide appropriate therapy by surgery, radiotherapy and/or hormonotherapy. In so-called oligo-metastatic disease targeted therapy may still be curative and prevent the disease from spreading to distant locations. Therefore it is of paramount importance to have an accurate tool of medical imaging to localize all possible locations to be treated. With some patients, the PSA-value is so low, that conventional nuclear medicine bone scanning or radiological CT or MRI cannot determine where the metastases are. Therefore, \[18F\]-Choline PET-CT was introduced to improve diagnostic imaging performance. However, in 30 to 40 percent of patients choline-PET does not localize tumor either, especially in small tumors and/or very low PSA values. The PSMA PET is already routinely used in many European centres, and has shown a superior accuracy in these patients as compared to conventional imaging techniques. This has been a very consistent finding in scientifically reported patient studies. Most of these investigations have been performed with PSMA labeled with Gallium-68. The investigators in Ghent, as others, have labeled PSMA with Fluor-18. This tracer provides many advantages, including a higher production yield enabling more patients to be scanned. Also from a perspective of radioprotection and financial costs, Fluor-18 is a better choice. Moreover, several recent studies, comparing Fluor with Gallium modalities seem to suggest equivalent or better diagnostic results, possibly because of a lower aspecific background activity.
Interventions
DIAGNOSTIC_TEST18F-PSMA
18F-PET imaging
Sponsors
University Hospital, Ghent
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
intravenous \[18F\]-PSMA-11
Eligibility
Sex/Gender
MALE
Age
40 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Patients diagnosed with prostate cancer, either in the setting of diagnosis of biochemical recurrence after curative treatment (prostatectomy with or without lymphadenectomy or radiotherapy), or at primary diagnosis and staging.
Exclusion criteria
* Age \< 40 or \> 70 years in phase-1; upper age limit is not applicable for the phase-2 trial. Most patients will be \> 65 years old, an estimate may be more than 80%. * Physically or mentally unfit to perform the sequential procedures * Refusal of patient to be informed about accidental findings on scans.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety of administration - ALT | before and 300 minutes after 18F-PSMA administration | Changes in ALT concentration in serum (expressed in U/L) |
| Safety of administration - creatinine | before and 300 minutes after 18F-PSMA administration | Changes in creatinine concentration in serum (expressed in mg/dL) |
| Safety of administration - AST | before and 300 minutes after 18F-PSMA administration | Changes in AST concentration in serum (expressed in U/L) |
| Safety of administration - Alkaline phosphatase | before and 300 minutes after 18F-PSMA administration | Changes in alkaline phosphatase concentration in serum (expressed in U/L) |
| Safety of administration - follow up of adverse events | Adverse events are followed up until 24 hours after PSMA administration. | Follow up of treatment-related adverse events according to CTCAE v4.0 criteria. |
| Safety of administration - change in blood pressure | hourly checking of blood pressure from timepoint of 18F-PSMA-11 injection up to 5 hours post 18F-PSMA injection | Changes in blood pressure (systolic and diastolic, expressed in mm Hg) |
| Biodistribution of 18F-PSMA | 0 to 300 minutes after 18F-PSMA administration | Follow up of 18F-PSMA distribution over time in blood, urine, and organs. 18F-PSMA |
| Safety of administration - change in temperature | hourly checking of temperature from timepoint of 18F-PSMA-11 injection up to 5 hours post 18F-PSMA injection | Changes in temperature (expressed in °C) |
| Safety of administration - change in heart rate | hourly checking of heart rate from timepoint of 18F-PSMA-11 injection up to 5 hours post 18F-PSMA injection | Changes in heart rate (expressed in beats per min) |
| Safety of administration - erythrocytes | before and 300 minutes after 18F-PSMA administration | Changes in erythrocytes count in plasma (expressed in 10\^6/µL) |
| Safety of administration - haemoglobin | before and 300 minutes after 18F-PSMA administration | Changes in haemoglobin concentration in plasma (expressed in g/dL) |
| Safety of administration - leukocytes | before and 300 minutes after 18F-PSMA administration | Changes in leukocytes count in plasma (expressed in 10\^3/µL) |
| Safety of administration - thrombocytes | before and 300 minutes after 18F-PSMA administration | Changes in thrombocytes count in plasma (expressed in 10\^3/µL) |
| Safety of administration - sodium | before and 300 minutes after 18F-PSMA administration | Changes in sodium concentration in serum(expressed in mmol/L) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Investigation of the stability of 18F-PSMA over time in plasma | 0 to 300 minutes after 18F-PSMA administration | The stability of 18F-PSMA will be assessed via measurement of the percentage defluorination of the compound. Free 18F will be separated from 18F-PSMA using solid-phase extraction, radioactivity (kBq/cc) of each fraction will be measured. |
| Establishment of critical organs | 0 to 300 minutes after 18F-PSMA administration | Based on the biodistribution of 18F-PSMA (primary outcome 14), it will be investigated which organs receive the highest radiation dose (expressed in mGy/MBq). |
Countries
Belgium
Outcome results
None listed