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Long Acting LHRH Versus Short Acting LHRH in the Treatment of Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
luteinizing hormone-releasing hormone (LHRH) short acting or long acting
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate cancer, LHRH, hormone therapy, testosterone level

Eligibility Criteria

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

Inclusion Criteria: All patients who elect to undergo brachytherapy for the treatment of adenocarcinoma of the prostate and who are otherwise recommended treatment with LHRH agonist. All patients must have a confirmed histological diagnosis of adenocarcinoma of the prostate and elect to be treated with transperineal implantation of the prostate. Eligible patients will have confirmed clinical stage T1 or T2 (UICC 1997 staging system) with PSA > 10 but < 15 and Gleason score < 7, OR PSA < 10 and Gleason score = 7 OR Prostate volume > 50cc as measured on trans rectal ultrasound While criteria 1 and 2 are mutually exclusive, criteria 3 can be present alone or in combination with criteria 1 OR 2. Otherwise patients should be able to give informed consent and have a life expectancy. 2 years. Exclusion Criteria: -

Sites / Locations

  • BC Cancer Agency - Vancouver Island CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Leuprolide preparations

Arm Description

One versus three-month Leuprolide preparations in patients otherwise suitable for our Brachytherapy Program

Outcomes

Primary Outcome Measures

The primary objective of this study is the median time to testosterone recovery in patients receiving 6 X 1-month or 2 X 3-month LHrH preparations and TPIP as radical treatment for limited stage prostate cancer.
In this context, testosterone recovery is defined as the return to the lower limit of normal for the patient's age group as well as return to pre treatment levels.

Secondary Outcome Measures

PSA profile, quality of life, sexual function

Full Information

First Posted
September 11, 2005
Last Updated
April 9, 2013
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT00175383
Brief Title
Long Acting LHRH Versus Short Acting LHRH in the Treatment of Prostate Cancer
Official Title
A Randomized Trial of Short Versus Long Acting LHRH Agonist Preparation Prior to Transperineal Implantation of the Prostate
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Unknown status
Study Start Date
June 2004 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Brachytherapy, or Transperineal implantation of the prostate (TPIP), is a recognized form of treatment for localized cancer of the prostate. TPIP has been used at the British Columbia Cancer Agency (BCCA) since 1998. As part of the treatment, some patients also require hormone therapy for 6 months. This is given as injections of a drug called an LHRH agonist. The LHRH agonist is made either as short-acting (1-month) or long-acting (3 month) injections. The LHRH agonist lowers testosterone levels, which helps make delivery of TPIP easier, and more effective. There are specific guidelines regarding the use of LHRH agonist treatment with brachytherapy, however there is no policy whether short-acting or long-acting LHRH agonists should be used. Analysis of results from BC has shown that there seems to be a delay in the time in which testosterone levels return to normal in men who receive the long-acting LHRH agonist compared with the short-acting LHRH agonist, however this is not known for sure.
Detailed Description
The suppression of testosterone to castrate levels has a definite advantage in terms of prostate volume downsizing, disease control and ease of Brachytherapy, in this patient population. The improved potency preservation rate seen with brachytherapy, when compared to other treatments such as radical prostatectomy or external beam, may be an important determinant in the patient's choice of treatment modality. Hence, testosterone recovery should be an important endpoint to consider in this patient population since prolongation of testosterone suppression may also delay the return of erectile function. In order to compare the impact of LHRH agonist preparations on the rate of testosterone recovery, we propose a randomized clinical trial using one versus three-month Leuprolide preparations in patients otherwise suitable for our Brachytherapy Program. The primary objective of this study is the median time to testosterone recovery in patients receiving 6 X 1-month or 2 X 3-month LHrH preparations and TPIP as radical treatment for limited stage prostate cancer. In this context, testosterone recovery is defined as the return to the lower limit of normal for the patient's age group as well as return to pre treatment levels. Analysis will mainly focus on time to testosterone recovery as defined by return to the lower limit of normal for the patient's age group as well as return to pre treatment levels. The lower limits of normal are defined as 5.8nmol/L and 5.5nmol/L for < 50 and > 50 years old Changes in PSA level, QOL and erectile function will also be recorded

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate cancer, LHRH, hormone therapy, testosterone level

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Leuprolide preparations
Arm Type
Experimental
Arm Description
One versus three-month Leuprolide preparations in patients otherwise suitable for our Brachytherapy Program
Intervention Type
Drug
Intervention Name(s)
luteinizing hormone-releasing hormone (LHRH) short acting or long acting
Intervention Description
See Detailed Description.
Primary Outcome Measure Information:
Title
The primary objective of this study is the median time to testosterone recovery in patients receiving 6 X 1-month or 2 X 3-month LHrH preparations and TPIP as radical treatment for limited stage prostate cancer.
Time Frame
6 months
Title
In this context, testosterone recovery is defined as the return to the lower limit of normal for the patient's age group as well as return to pre treatment levels.
Secondary Outcome Measure Information:
Title
PSA profile, quality of life, sexual function

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients who elect to undergo brachytherapy for the treatment of adenocarcinoma of the prostate and who are otherwise recommended treatment with LHRH agonist. All patients must have a confirmed histological diagnosis of adenocarcinoma of the prostate and elect to be treated with transperineal implantation of the prostate. Eligible patients will have confirmed clinical stage T1 or T2 (UICC 1997 staging system) with PSA > 10 but < 15 and Gleason score < 7, OR PSA < 10 and Gleason score = 7 OR Prostate volume > 50cc as measured on trans rectal ultrasound While criteria 1 and 2 are mutually exclusive, criteria 3 can be present alone or in combination with criteria 1 OR 2. Otherwise patients should be able to give informed consent and have a life expectancy. 2 years. Exclusion Criteria: -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shelley Hordiyuk, BSc., MBA
Phone
250-519-5512
Email
SHordiyu@bccancer.bc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Eric Berthelet, MD
Organizational Affiliation
The University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
BC Cancer Agency - Vancouver Island Centre
City
Victoria
State/Province
British Columbia
ZIP/Postal Code
V8R 6V5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shelley Hordiyuk, BSc., MBA
Phone
250-519-5512
First Name & Middle Initial & Last Name & Degree
Howard Pai

12. IPD Sharing Statement

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Long Acting LHRH Versus Short Acting LHRH in the Treatment of Prostate Cancer

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