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Clinical Trials/NCT03067389
NCT03067389
Completed
Not Applicable

Evaluation of a Combined Breast Cancer Risk Derived From a Polygenic Risk Score and the Tyrer-Cuzick Model

Myriad Genetic Laboratories, Inc.4 sites in 1 country553 target enrollmentFebruary 6, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hereditary Cancer
Sponsor
Myriad Genetic Laboratories, Inc.
Enrollment
553
Locations
4
Primary Endpoint
To demonstrate that a combined breast cancer risk derived from a polygenic risk score and a breast cancer risk assessment model is a better predictor of breast cancer than the risk assessment model alone
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

A prospective, non-interventional study in women 18 to 84 years of age. Subjects will provide a sample for genetic testing and information about their medical and family history. The results of the genetic test will be combined with clinical data to validate a method of predicting breast cancer risk.

Detailed Description

This is a prospective, non- interventional study. Women presenting at imaging centers for routine breast cancer screening or breast cancer diagnostic assessment and who provide written informed consent will undergo genetic testing. Subjects will also provide information about their personal medical and cancer history and family cancer history. The results of the genetic test will be combined with the subject's clinical information, family history, and a risk assessment model to validate a new method of predicting breast cancer.

Registry
clinicaltrials.gov
Start Date
February 6, 2016
End Date
January 8, 2019
Last Updated
7 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women without breast cancer:
  • 18 to 84 years of age
  • Western/Northern European, Central/Eastern European, or Ashkenazi ancestry
  • No history of invasive breast cancer
  • Women with a history of breast cancer:
  • 18 to 84 years of age
  • Western/Northern European, Central/Eastern European, or Ashkenazi ancestry
  • Pathologically confirmed invasive breast cancer diagnosed within the past 12 months

Exclusion Criteria

  • Unwilling to provide written informed consent
  • Women with history of ductal carcinoma in situ (DCIS).
  • Patient has had a prior breast biopsy, exclusive of a breast biopsy diagnostic of breast cancer, that showed either hyperplasia, atypical hyperplasia, lobular carcinoma in situ (LCIS), or the specific histologic result is unknown to the patient

Outcomes

Primary Outcomes

To demonstrate that a combined breast cancer risk derived from a polygenic risk score and a breast cancer risk assessment model is a better predictor of breast cancer than the risk assessment model alone

Time Frame: Baseline

Secondary Outcomes

  • To derive a distribution of polygenic risk scores in an unselected patient population(baseline)

Study Sites (4)

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