Prospective Registry of Multiplex Testing (PROMPT)
| Status: | Recruiting | 
|---|---|
| Healthy: | No | 
| Age Range: | 18 - Any | 
| Updated: | 3/2/2019 | 
| Start Date: | January 2016 | 
| End Date: | January 2020 | 
| Contact: | Mark Robson, MD | 
| Phone: | 646-888-4058 | 
Prospective Registry of Multiplex Testing (PROMPT): Phase II
This study is being done to learn more about how changes in certain genes may be linked to
cancer. Some people with cancer got their disease because they inherited an abnormal
(mutated) gene.
The researchers of this study want to better understand the risks that are linked to genetic
changes in these less well-studied genes. By understanding these risks, we believe that
doctors will be able to give better advice to families with mutations in these genes.
			cancer. Some people with cancer got their disease because they inherited an abnormal
(mutated) gene.
The researchers of this study want to better understand the risks that are linked to genetic
changes in these less well-studied genes. By understanding these risks, we believe that
doctors will be able to give better advice to families with mutations in these genes.
PROMPT (Prospective Registry of Multiplex Testing) is an Internet-based, patient-directed
ascertainment study. It is a partnership between Memorial Sloan Kettering, University of
Pennsylvania, Mayo Clinic, and Dana Farber Cancer Institute in collaboration with Ambry
Genetics, GeneDx, Myriad Genetics, Pathway Genomics, and Quest Laboratories (5 laboratories
providing multiplex panel testing commercially).
ascertainment study. It is a partnership between Memorial Sloan Kettering, University of
Pennsylvania, Mayo Clinic, and Dana Farber Cancer Institute in collaboration with Ambry
Genetics, GeneDx, Myriad Genetics, Pathway Genomics, and Quest Laboratories (5 laboratories
providing multiplex panel testing commercially).
Inclusion Criteria:
- Individual with deleterious (pathogenic) or likely deleterious (likely pathogenic)
mutation in a cancer susceptibility gene OR
- Individual with a variant of uncertain significance (VUS) in a cancer susceptibility
gene OR
- Family members, either tested or not tested, who are part of a family known to be
transmitting a deleterious or likely deleterious mutation or a variant of uncertain
significance in a cancer predisposition gene
Exclusion Criteria:
- Inability or refusal to participate in consent discussion
- Subject is less than 18 years old
We found this trial at
    10
    sites
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									136 Mountainview Boulevard
Basking Ridge, New Jersey 07920
	
			
					Basking Ridge, New Jersey 07920
Phone: 646-888-4058
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		Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...  
  
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									650 Commack Rd
Commack, New York 11725
	
			Commack, New York 11725
(631) 623-4000
							 
					Phone: 646-888-4058
					
		Memorial Sloan-Kettering Cancer Center at Commack Memorial Sloan Kettering Cancer Center - the world's oldest...  
  
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									1275 York Ave
New York, New York 10021
	
			New York, New York 10021
(212) 639-2000
							 
					Principal Investigator: Mark Robson, MD
			
						
										Phone: 646-888-4058
					
		Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...  
  
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		Univ of Pennsylvania Penn has a long and proud tradition of intellectual rigor and pursuit...  
  
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									200 First Street SW
Rochester, Minnesota 55905
	
			Rochester, Minnesota 55905
507-284-2511 
							 
					Phone: 507-538-3270
					
		Mayo Clinic Cancer Center The Mayo Clinic Cancer Center is a National Cancer Institute-designated comprehensive...  
  
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									1000 North Village Avenue
Rockville Centre, New York 11570
	
			
					Rockville Centre, New York 11570
Phone: 646-888-4058
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