Official Title
Capturing BRCA1/2 Mutational Status in Women With High Grade Serous Ovarian Cancer and Impact on Clinical Outcome.
Brief Title
Capturing BRCA1/2 Mutational Status in Women With High Grade Serous Ovarian Cancer and Impact on Clinical Outcome.
Protocol ID
NCT02341118
Lead Sponsor
University Health Network, Toronto
Brief Summary
BRCA1 or BRCA2 genes, are implicated in 10-15% of ovarian cancer cases, increased to 22%
germline BRCA1/2 mutation frequency in patients with high grade serous histology subtype,
including those women who have no family history of breast or ovarian cancer. With the
rapid advancement of therapeutics targeted this population, this protocol seeks to
provide genetic BRCA1/2 screening to all patients with high grade serous ovarian cancer.
This information may help in selection of future treatment options and genetic testing
for BRCA1/2 may be used to potentially prevent a proportion of cancer for the family
members.
This study will be an opportunity for patient to improve access at genetic and molecular
testing for BRCA1/2 mutation which could impact her future treatment option. Moreover,
this study will allow to prospectively assess the proportion of patients with BRCA
mutation in ovarian cancer and describe the type of mutations identified in a large
population.
Detailed Description
Primary Objectives
· To provide genomic profiling for BRCA1 and BRCA2 mutational status in patients' with
high grade serous ovarian cancer.
Secondary Objectives
- To track the number of women with high grade serous ovarian cancer who are being
screened in Princess Margaret Cancer Center for mutations in BRCA1/2
- To track accrual rates and clinical outcomes in patients with high grade serous
ovarian cancer who are BRCA1/2-positive
- To correlate impact of BRCA1/2 mutational status on clinical outcome
- To track utilization of genetic counseling services at Princess Margaret Cancer
Centre
Enrollment Count
109 participants
Eligibility Criteria
Inclusion Criteria:
- Patients with high grade serous carcinoma originating from the ovaries, fallopian
tube or peritoneal cavity; subtype of high grade endometrioid and clear cell ovarian
cancer could be eligible in the exploratory cohort
- Patient must be ≥18 years old
- All patients must have sufficient archival tumor tissue for molecular analysis
- All patients must consent to have a genetic testing
- All patients must have signed and dated an informed consent form
Exclusion Criteria:
· Other histology subtype
Filters
Ovarian Cancer
TERMINATED
ADULT
OLDER_ADULT