Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Unknown status
CT.gov ID
NCT02631616
Collaborator
(none)
30
1
24.9

Study Details

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.

Condition or Disease Intervention/Treatment Phase
Phase 1

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:
  1. To detect biochemical response (PSA and chromogranin A)

  2. To detect PET response (in repeated PET/CT, 68Ga-DOTATET).

  3. To detect clinical response (QOL 30 questioner).

  4. To detect adverse response.

Materials and Methods:
  1. 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

  2. Treatment with monthly injections of Sandoatatin LAR - 30mg will be initiated.

  3. 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Treatment With Sandostatin in Patients With Castrate Resistance Prostate Cancer Showing Uptake of 68Ga-DOTATET
Study Start Date :
Feb 1, 2016
Anticipated Primary Completion Date :
Feb 1, 2017
Anticipated Study Completion Date :
Mar 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment arm

Monthly injections of Somatostatin (Sandoatatin LAR - 30mg)

Drug: Somatostatin
Monthly injections of Somatostatin
Other Names:
  • Sandoatatin LAR - 30mg
  • Outcome Measures

    Primary Outcome Measures

    1. Clinical response [4 months]

      QOL 30 questioner

    Secondary Outcome Measures

    1. Biochemical response [4 months]

      Blood test for PSA (in ng/ml)

    2. Imaging response [4 months]

      PET/CT with 68Ga-DOTATET

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Hadassah Medical Organization

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ofer Gofrit, Prof. Ofer N. Gofrit, MD, PhD, Hadassah Medical Organization
    ClinicalTrials.gov Identifier:
    NCT02631616
    Other Study ID Numbers:
    • NEPros-HMO-CTIL
    First Posted:
    Dec 16, 2015
    Last Update Posted:
    Dec 16, 2015
    Last Verified:
    Dec 1, 2015
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Ofer Gofrit, Prof. Ofer N. Gofrit, MD, PhD, Hadassah Medical Organization
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 16, 2015