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Trial registered on ANZCTR
Registration number
ACTRN12618001696280
Ethics application status
Approved
Date submitted
28/09/2018
Date registered
15/10/2018
Date last updated
15/10/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Detecting new bone metastases in patients on androgen deprivation therapy
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Scientific title
Assessing the emergence of new bone lesions in primary prostate cancer patients at high risk of bone metastasis starting androgen deprivation therapy: Implications for current treatment intervention
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Secondary ID [1]
296094
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Nil Known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Prostate Cancer
309673
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Condition category
Condition code
Cancer
308475
308475
0
0
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Prostate
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Cancer
308476
308476
0
0
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Bone
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This study aims to improve knowledge around the way that cancer spreads in men with advanced prostate cancer who receive targeted radiation therapy and androgen deprivation therapy (ADT).
This study does not direct treatment and any treatment decisions will be based on the recommendation of your treating doctor. This study is looking at the effects on bone lesions in individuals receiving this treatment. At study enrolment a 68Ga-PSMA PET CT scan will occur as part of standard of care treatment.
A 68Ga-PSMA PET CT is a nuclear medicine imaging test used in prostate cancer and it has higher diagnostic efficacy than conventional imaging. Radioactive tracers are injected and then taken up by tissues in your body. Activity within your organs are then detected by the PET scanner which shows how tissue and organs are working. This test takes approximately 2 hours with the scan itself taking up to half an hour. This nuclear medicine examination is considered safe with almost no reported adverse reactions attributable to the radiopharmaceuticals used.
This study requires two additional 68Ga-PSMA PET CT scans that are beyond standard of care. These scans occur at 6 and 12 months post enrolment. There are also optional blood tests that occur at enrolment, 6 and 12 months post enrolment. Blood tests are at the discretion of the individual participant.
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Intervention code [1]
312435
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Diagnosis / Prognosis
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Intervention code [2]
312525
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Early detection / Screening
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Comparator / control treatment
No Control Group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
307455
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Number of new bone lesions identified on 68Ga-PSMA PET CT scan
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Assessment method [1]
307455
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Timepoint [1]
307455
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At 6 months and 12 months post enrolment
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Secondary outcome [1]
351968
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The proportion of participants who started bisphosphonates or other therapeutics designed to block bone reabsorption as measured by medication history
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Assessment method [1]
351968
0
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Timepoint [1]
351968
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At 12 months post enrolment
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Secondary outcome [2]
352507
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Change in Lactate dehydrogenase (LDH) levels in blood from baseline
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Assessment method [2]
352507
0
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Timepoint [2]
352507
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6 and 12 months post enrolment
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Secondary outcome [3]
352839
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Change in complete blood count (CBC) levels in blood from baseline
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Assessment method [3]
352839
0
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Timepoint [3]
352839
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6 and 12 months post enrolment
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Secondary outcome [4]
352840
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Change in electrolytes urea creatinine (EUC) levels in blood from baseline
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Assessment method [4]
352840
0
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Timepoint [4]
352840
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6 and 12 months post enrolment
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Secondary outcome [5]
352841
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Change in calcium-magnesium-phosphate (CMP) levels in blood from baseline
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Assessment method [5]
352841
0
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Timepoint [5]
352841
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6 and 12 months post enrolment
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Secondary outcome [6]
352842
0
Change in Testosterone levels in blood from baseline
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Assessment method [6]
352842
0
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Timepoint [6]
352842
0
6 and 12 months post enrolment
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Secondary outcome [7]
352843
0
Change in liver function test (LFT) levels in blood from baseline
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Assessment method [7]
352843
0
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Timepoint [7]
352843
0
6 and 12 months post enrolment
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Secondary outcome [8]
352844
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Change in prostate specific antigen (PSA) levels in blood from baseline
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Assessment method [8]
352844
0
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Timepoint [8]
352844
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6 and 12 months post enrolment
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Eligibility
Key inclusion criteria
- Pathologically confirmed adenocarcinoma of prostate
- Men presenting high risk of metastatic disease.
- Gleason score 7-10
- Deemed suitable by a medical oncologist to start targeted radiation therapy and androgen deprivation therapy.
- Blood tests:
a) haemoglobin > 100g/L
b) Platelets > 100 x 10^9/L
c) Total white cell count > 4 x 10^9/L
-Willingness to give written, informed consent and willingness to participate in and comply with the study.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Participants whose prostate cancer is not high risk of metastasis;
- Participants who refuse to join the trial or are unable consent;
- Participants who cannot remain still for at least 30 minutes to comply with imaging requirements.
- Participants who have no PSMA receptor activity (approximately 5-10% of the population) and provide a negative baseline scan.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Not Applicable
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/11/2018
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Actual
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Date of last participant enrolment
Anticipated
1/05/2019
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Actual
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Date of last data collection
Anticipated
1/05/2020
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Actual
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Sample size
Target
10
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
11912
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St Vincent's Hospital (Darlinghurst) - Darlinghurst
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Recruitment postcode(s) [1]
24049
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2010 - Darlinghurst
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Funding & Sponsors
Funding source category [1]
300682
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Charities/Societies/Foundations
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Name [1]
300682
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The Prostate Cancer Foundation of Australia
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Address [1]
300682
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Level 3
39-41 Chandos Street
St Leonards
NSW 2065
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Country [1]
300682
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Australia
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Primary sponsor type
Other Collaborative groups
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Name
The Garvan Institues of Medical Research
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Address
384 Victoria St
Darlinghurst
NSW, 2010
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Country
Australia
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Secondary sponsor category [1]
300211
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None
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Name [1]
300211
0
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Address [1]
300211
0
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Country [1]
300211
0
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Other collaborator category [1]
280353
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Hospital
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Name [1]
280353
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St Vincent's Hosptial (Darlinghurst)
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Address [1]
280353
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370 Victoria St
Darlinghurst
NSW 2010
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Country [1]
280353
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
301464
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St Vincent's Hospital Human Research Ethics Committee
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Ethics committee address [1]
301464
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Translational Research Centre 97-105 Boundary Street Darlinghurst NSW 2010
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Ethics committee country [1]
301464
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Australia
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Date submitted for ethics approval [1]
301464
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27/11/2017
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Approval date [1]
301464
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16/09/2018
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Ethics approval number [1]
301464
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HREC/17/SVH/375
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Summary
Brief summary
This study's purpose is to assess new bones lesion(s) in prostate cancer participants starting androgen deprivation therapy (ADT). Who is it for? You may be eligible to join this study if you have prostate cancer with a high risk of metastatic disease and your treating doctor recommends starting ADT and targeted radiotherapy. Study Details: Participants in this study will undergo a 68Ga-PSMA PET CT at study entry. Participants will have two additional 68Ga-PSMA PET CT at 6 and 12 months. Participants will be followed up per routine clinical care. Participants have the option of providing optional blood test. It is hoped that this research will provide insight in the incidence and mechanism of bone lesions in advanced prostate cancer.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Peter Croucher
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Address
87098
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The Garvan Institute of Medical Research
Bone Biology Division
384 Victoria St
Darlinghurst
NSW 2010
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Country
87098
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Australia
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Phone
87098
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+612 9292 8243
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Fax
87098
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Email
87098
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[email protected]
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Contact person for public queries
Name
87099
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Matthew Summers
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Address
87099
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The Garvan Institute of Medical Research
Bone Biology Division
384 Victoria St
Darlinghurst
NSW 2010
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Country
87099
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Australia
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Phone
87099
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+61 415803747
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Fax
87099
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Email
87099
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[email protected]
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Contact person for scientific queries
Name
87100
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Matthew Summers
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Address
87100
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The Garvan Institute of Medical Research
Bone Biology Division
384 Victoria St
Darlinghurst
NSW 2010
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Country
87100
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Australia
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Phone
87100
0
+61 415803747
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Fax
87100
0
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Email
87100
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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