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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
Hadassah Medical Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with histologically proven prostate cancer.
  2. Hormonal treatment (either surgical orchiectomy or medical castration with LHRH agonist or antagonist).
  3. Proven castration levels (serum Testosterone< 50 ng/dl)
  4. Radiological evidence of metastatic disease.
  5. 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

    First Posted
    December 3, 2015
    Last Updated
    December 11, 2015
    Sponsor
    Hadassah Medical Organization
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    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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