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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04316507
Other study ID # 437-2019
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2020
Est. completion date March 31, 2021

Study information

Verified date October 2020
Source Sunnybrook Health Sciences Centre
Contact Andrea Eisen, MD
Phone 416 4804617
Email andrea.eisen@sunnybrook.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pancreatic cancer (PC) has a dismal prognosis. Approximately 10% of PC patients carry a germline pathogenic variant in a cancer susceptibility gene, whose identification can lead to better treatments for the patient and participation in cancer prevention programs for their family members. Conventional genetic testing for PC patients is based on the family history of cancer, and may take up to six months from the point of meeting with the treating physician to receiving the results from a genetic counsellor. The median overall survival for these patients is 6 - 12 months, which may prevent them from having the genetic testing in the first place, or from receiving further targeted treatments. Patients with PC need a more comprehensive knowledge of their disease for better treatment planning. This includes genetic testing in absence of family history of cancer. The investigators designed a one year study to assess the feasibility of medical oncologist initiated cancer genetic testing for all newly diagnosed PC patients unselected by family history. For patients with negative genetic testing, no further testing will be ordered after the disclosure of results. Patients with positive genetic testing results will be informed and referred to Cancer Genetics Clinic. The investigators expect to enroll 100 patients in 1 year. Patients will be asked to complete satisfaction questionnaires according to the Satisfaction with Genetic Counseling Scale in multiple time points (pre-testing, post-testing, at 6 months and at 12 months). Designated oncologists will be asked to evaluate the process using the Oncologist Satisfaction Survey after every five counseled patients. Three primary objectives will include 1) assessment of the turnaround time for genetic testing results; 2) assessment of patient satisfaction; 3) assessment of oncologist's satisfaction. Secondary objectives will include assessment of association between genetic testing results and types of treatment and overall survival.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 31, 2021
Est. primary completion date March 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - • Newly diagnosed exocrine pancreatic cancer - Patient consents to blood draw and genetic testing - Treating oncologist at Odette Cancer Centre - No conditions that would prevent patients from completing the study-related questionnaires or understanding the consent process - Valid phone number - Email address to send link to online family history questionnaire - Treating physician agrees to complete the referrals Exclusion Criteria: - Patient declines genetic testing - Blood transfusion within the past month - Allogenic bone marrow transplantation - History of comprehensive panel genetic testing

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Genetic Counselling and Testing
Oncologist-initiated brief genetic counselling and testing

Locations

Country Name City State
Canada Sunnybrook Odette Cancer Centre Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Days from decision to test to receiving genetic test results 1 year
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