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Trial registered on ANZCTR
Registration number
ACTRN12618001553268
Ethics application status
Approved
Date submitted
27/06/2018
Date registered
17/09/2018
Date last updated
17/09/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Metastatic Access Research Collaboration (MonARC) for collection of post-mortem tissue
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Scientific title
Metastatic Access Research Collaboration for collection of post-mortem tissue
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Secondary ID [1]
295342
0
Nil known
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Universal Trial Number (UTN)
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Trial acronym
MonARC
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Metastatic Cancers
308548
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Condition category
Condition code
Cancer
307516
307516
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0
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Any cancer
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
1
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Target follow-up type
Years
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Description of intervention(s) / exposure
Metastatic Access Research Collaboration (MonARC) study is research project that aims to improve knowledge around the way that cancer spreads and becomes resistant to treatment. In this study, we seek permission to obtain and study samples of tissue from patients who have recently died of their cancer. This procedure is called an autopsy or post-mortem examination.
Should you have terminal cancer and wish to consent to the project, a blood sample (40ml) will be taken after you consent. This will be to perform laboratory tests about your DNA.
Samples will be collected during the autopsy from sites containing cancerous cells. The study team will follow the request of the participant or their family if certain body sections are not to be removed.
Following the autopsy, samples may be used in projects that are currently Human Research Ethics Committee (HREC) approved or stored for future research (a "Biobank"). Tissues will be stored indefinitely until used for research. Health information or biological samples will NOT be used on research project without the permission of a Human Research Ethics Committee.
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Intervention code [1]
301665
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Not applicable
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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]
306489
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Number of cancerous tissue available for medical research
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Assessment method [1]
306489
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Timepoint [1]
306489
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3 years
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Secondary outcome [1]
349395
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Number of patient derived xenograph models of cancer
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Assessment method [1]
349395
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Timepoint [1]
349395
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3 years
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Eligibility
Key inclusion criteria
1, Metastatic malignancy
2, Ability to make informed consent
3, Have received and understood information from their treating doctor that their disease is terminal
4. Are treated or have been seen at a Participating Site, engaging in services including but not limited to medical oncology, palliative care or allied health.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. There is concern that involvement will have negative psychological impact on the individual or his/her family.
2. They are currently incarcerated
3. They have unstable psychiatric illness
4. A health-care provider (HCP) involved in the patient care OR any listed study personnel, feels that the autopsy is inappropriate
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
This is an exploratory study and no power calculations are provided.
The study team expect that less that 20% of eligible participants will consent. Furthermore, if after the participant death, a family member does not wish for the procedure to be performed, we will not proceed with autopsy.
Statistically significant information is expected from low number of participants. Campbell et al. (2010) showed unparalleled view of the timing, sequence and diversity of changes in pancreatic cancer with only 17 pancreatic cancer patients who underwent rapid autopsy.
It is therefore expected 100 patients across all cancer types will provide useful insights into the spreading of cancer types and development of resistance to treatment .
Campbell, P.J., et al., The patterns and dynamics of genomic instability in metastatic pancreatic cancer. Nature, 2010. 467(7319): p. 1109-1113.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
19/02/2018
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Date of last participant enrolment
Anticipated
1/02/2021
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Actual
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Date of last data collection
Anticipated
1/02/2022
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Actual
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Sample size
Target
100
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Accrual to date
4
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
11255
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St Vincent's Hospital (Darlinghurst) - Darlinghurst
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Recruitment postcode(s) [1]
23132
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2010 - Darlinghurst
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Funding & Sponsors
Funding source category [1]
299935
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Hospital
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Name [1]
299935
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St Vincent's Hospital Sydney
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Address [1]
299935
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The Kinghorn Cancer Centre
370 Victoria St
Darlinghurst
NSW 2010
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Country [1]
299935
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Australia
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Funding source category [2]
299936
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Other Collaborative groups
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Name [2]
299936
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Garvan Institute of Medical Research
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Address [2]
299936
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370 Victoria St
Darlinghurst
NSW 2010
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Country [2]
299936
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Australia
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Primary sponsor type
Hospital
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Name
St Vincent's Hospital Sydney
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Address
390 Victoria St
Darlinghurst
NSW 2010
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Country
Australia
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Secondary sponsor category [1]
299311
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None
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Name [1]
299311
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Address [1]
299311
0
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Country [1]
299311
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
300801
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St Vincent’s Hospital Human Research Ethics Committee
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Ethics committee address [1]
300801
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390 Victoria St Darlinghurst NSW 2010
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Ethics committee country [1]
300801
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Date submitted for ethics approval [1]
300801
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10/08/2017
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Approval date [1]
300801
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12/09/2017
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Ethics approval number [1]
300801
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HREC/17/SVH254
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Summary
Brief summary
The purpose of this research is to: 1. Create a library (“biorepository”) of cancer samples to use in future research projects. 2. Collect medical information about patients to put with the cancer samples. 3. Keep some cells to grow in the laboratory (“cell lines”) and grow pieces of cancer tissue in specially bred mice (“xenografting”). Who is it for? You may be eligible for this study if you are an adult who has been diagnosed with metastatic cancer. Study details Participants will be asked to provide a 40ml sample of blood after they have consented to the research and in the future allow for tissue collection post mortem. It is hoped that this research will provide important information on how cancer cells grow, change over time and spread. This information is essential to help design more effective therapies for cancer patients in the future. This research is being conducted by the Garvan Institute of Medical Research and The Kinghorn Cancer Centre.
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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
84858
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Prof Anthony Joshua
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Address
84858
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The Kinghorn Cancer Centre
370 Victoria St
Darlinghurst
NSW 2010
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Country
84858
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Australia
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Phone
84858
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+61 2 9355 5600
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Fax
84858
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+61 2 9355 5735
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Email
84858
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[email protected]
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Contact person for public queries
Name
84859
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Robert Kent
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Address
84859
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The Kinghorn Cancer Centre
370 Victoria St
Darlinghurst
NSW 2010
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Country
84859
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Australia
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Phone
84859
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+61 2 9355 5600
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Fax
84859
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+61 2 9355 5735
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Email
84859
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[email protected]
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Contact person for scientific queries
Name
84860
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Anthony Joshua
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Address
84860
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The Kinghorn Cancer Centre
370 Victoria St
Darlinghurst
NSW 2010
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Country
84860
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Australia
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Phone
84860
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+61 2 9355 5600
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Fax
84860
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+61 2 9355 5735
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Email
84860
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[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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