Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET
Primary Purpose
Prostatic Neoplasms
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Somatostatin
Sponsored by

About this trial
This is an interventional treatment trial for Prostatic Neoplasms focused on measuring Prostatic Neoplasma, Castration-Resistant, neuroendocrine differentiation, 68Ga-DOTATET, PET/CT
Eligibility Criteria
Inclusion Criteria:
- Patients with histologically proven prostate cancer.
- Hormonal treatment (either surgical orchiectomy or medical castration with LHRH agonist or antagonist).
- Proven castration levels (serum Testosterone< 50 ng/dl)
- Radiological evidence of metastatic disease.
- Uptake of the radiotracer 68Ga-DOTATET in at two least to metastases.
Exclusion Criteria:
1. Participation in another trial.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment arm
Arm Description
Monthly injections of Somatostatin (Sandoatatin LAR - 30mg)
Outcomes
Primary Outcome Measures
Clinical response
QOL 30 questioner
Secondary Outcome Measures
Biochemical response
Blood test for PSA (in ng/ml)
Imaging response
PET/CT with 68Ga-DOTATET
Full Information
NCT ID
NCT02631616
First Posted
December 3, 2015
Last Updated
December 11, 2015
Sponsor
Hadassah Medical Organization
1. Study Identification
Unique Protocol Identification Number
NCT02631616
Brief Title
Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET
Official Title
Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
February 2017 (Anticipated)
Study Completion Date
March 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hadassah Medical Organization
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Purpose: Castrate resistance prostate cancer (CRPC) often shows histological evidence of neuroendocrine differentiation (NED). Recently the investigators initiated a research project investigating the uptake of the radiotracer 68Ga-DOTATET (a marker of neuroendocrine tumors-NET) in PET/CT in patients with CRPC. In 4/8 patients studied thus far, uptake of the tracer in bone metastases was found. It has been shown that monthly injections of Somatostatin lengthen overall survival in patients with NET. The purpose of the current project is to examine the ability of Somatostatin to stabilize or possibly reverse metastases in patients with CRPC that express high level of somatostatin receptors in 68Ga-DOTATET PET/CT.
Materials and Methods: 30 patients with CRPC will be studied with 68Ga-DOTATET PET/CT. Patients showing uptake of the radiotracer 68Ga-DOTATET in at two least to metastases will be considered eligible for the study. These patients will be evaluated biochemically and clinically and will be treated with monthly injections of Sandoatatin LAR - 30mg. Clinical, biochemical and imaging studies (68Ga-DOTATET PET/CT) will be repeated after 4 and 12 months of treatment. Responding patients (stabilization or decrease in the number and SUV of metastases) will be subjected to continued therapy until progression.
Detailed Description
Introduction: Neuroendocrine tumors (NET) present receptors to somatostatin. This feature is utilized therapeutically in patients with metastatic NET. Monthly injection of Somatostatin was shown to lengthen overall survival (compared to placebo) in these patients. From histological studies it is known that advanced prostate cancer often shows neuroendocrine differentiation (NED). This is considered one of the mechanisms of "escape" of tumor cells from androgen deprivation therapy. Recently the investigatros initiated a research project investigating the uptake of the radiotracer 68Ga-DOTATET (a marker of neuroendocrine tumors-NET) in PET/CT in patients with castrate resistance prostate cancer. In 4/8 patients studied thus far, uptake of the tracer in bone metastases was found.
Purpose: The purpose of the current project is to examine the ability of LAR Somatostatin to stabilize or possibly reverse metastases in patients with castrate resistance prostate cancer that express high level of somatostatin receptors.
The aims of the study are:
To detect biochemical response (PSA and chromogranin A)
To detect PET response (in repeated PET/CT, 68Ga-DOTATET).
To detect clinical response (QOL 30 questioner).
To detect adverse response.
Materials and Methods:
Eligible patients will be evaluated by: serum levels of PSA, chromogranin A, Pro GRP and possibly other non-genetic markers and by QOL 30 questioner
Treatment with monthly injections of Sandoatatin LAR - 30mg will be initiated.
Evaluation will be done after 4 injections and will include: blood tests for PSA and chromogranin A, Pro GRP and possibly other non-genetic markers and by QOL 30 questioner and by PET/CT with 68Ga-DOTATET. Similar evaluation will be done after 12 injections. Responding patients (stabilization or decrease in the number and SUV of metastases) will be subjected to continued therapy until progression.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms
Keywords
Prostatic Neoplasma, Castration-Resistant, neuroendocrine differentiation, 68Ga-DOTATET, PET/CT
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Treatment arm
Arm Type
Experimental
Arm Description
Monthly injections of Somatostatin (Sandoatatin LAR - 30mg)
Intervention Type
Drug
Intervention Name(s)
Somatostatin
Other Intervention Name(s)
Sandoatatin LAR - 30mg
Intervention Description
Monthly injections of Somatostatin
Primary Outcome Measure Information:
Title
Clinical response
Description
QOL 30 questioner
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Biochemical response
Description
Blood test for PSA (in ng/ml)
Time Frame
4 months
Title
Imaging response
Description
PET/CT with 68Ga-DOTATET
Time Frame
4 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with histologically proven prostate cancer.
Hormonal treatment (either surgical orchiectomy or medical castration with LHRH agonist or antagonist).
Proven castration levels (serum Testosterone< 50 ng/dl)
Radiological evidence of metastatic disease.
Uptake of the radiotracer 68Ga-DOTATET in at two least to metastases.
Exclusion Criteria:
1. Participation in another trial.
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET
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