Clinical Trials Directory

Trials / Completed

CompletedNCT00945464

Scripps Polster Breast Care Center Investigational GeneBank

Status
Completed
Phase
Study type
Observational
Enrollment
1,136 (actual)
Sponsor
Scripps Translational Science Institute · Academic / Other
Sex
Female
Age
30 Years
Healthy volunteers
Accepted

Summary

Breast cancer is a disease of complex origin with a strong genetic component. The incidence of breast cancer is very high in monozygotic twins of patients, and it is thought that a high proportion and perhaps the majority of breast cancers arise in a small number of genetically susceptible women. Recent studies in human genetics have discovered several intervals in the human genome containing inherited variants that are statistically associated with the propensity to develop breast cancer. The investigators plan to use this knowledge to design a genetic screening test to guide recommendations for breast cancer screening with mammography. If the small group of genetically susceptible women can be identified, more effective breast cancer screening strategies can be implemented. In contrast, a very large proportion of women who undergo yearly mammography are at exceptionally low risk from a genetic perspective. Using genomic guidance could eventually reconfigure the most efficacious strategy to screen women for early detection of breast cancer. By developing a genetic screening panel based on genetic markers for breast cancer, the investigators will be able to more accurately determine a woman's individual risk for developing breast cancer.

Detailed description

Women the age of 30 or over who are undergoing screening or diagnostic breast imaging as an out patient at the Scripps Polster Breast Care Center in La Jolla, CA, with at least 5 years of historic breast imaging data available will be eligible to enroll. For this study, consecutive subjects who have completed screening or diagnostic breast imaging at the Scripps Polster Breast Care Center will be enrolled for one day. It is estimated that up to 5000 subjects will be included in the cohort.

Conditions

Interventions

TypeNameDescription
OTHERBlood/saliva samples, historic breast imagingSubjects are required only to provide a blood or saliva sample, relevant personal and family history (if available), and 5 years of historic breast imaging reports.

Timeline

Start date
2008-07-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2009-07-24
Last updated
2015-10-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00945464. Inclusion in this directory is not an endorsement.