Official Title: Genetic Information to Inform Treatment and Screening GIFTS Study for Prostate Cancer
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: GIFTS
Brief Summary: This trial studies the role of inherited present at birth mutations in cancer risk genes such as BRCA2 BRCA1 ATM CHEK2 and others in relation to prostate cancer This study may help researchers understand the frequency and importance of inherited mutations in cancer risk genes in patients with prostate cancer and potentially help identify better ways to treat cancer in patients who have a mutation in one of these genes
Detailed Description: OUTLINE
Participants complete questionnaire over 20 minutes at baseline then undergo collection of saliva sample for genetic testing Participants identified to have an inherited mutation in a deoxyribonucleic acid DNA repair gene undergo genetic counseling Participants whose genetic testing does not indicate an inherited mutation in a DNA repair gene receive a letter thanking them for their participation and emphasizing the importance of ongoing communication with their physician and family members about cancer risk
Participants will be sent newsletters every year to encourage study engagement and update health questionnaires every two years
Study Oversight
Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID
Type
Domain
Link
P50CA097186
NIH
None
None
NCI-2020-00933
REGISTRY
None
None
8754
OTHER
Fred HutchUniversity of Washington Cancer Consortium