ARTEMIS: Study of Patients With Early Stage Pancreatic Cancer Who Have Undergone Genetic Testing

Stopped early

Conditions studied: Pancreatic Adenocarcinoma, Pancreatic Cancer, Resectable Pancreatic Cancer

In brief

This study includes participants with pancreatic cancer who are undergoing genetic testing at Invitae related to their diagnosis of pancreatic cancer. Our goal in this study is two-fold. First, we would like to research whether any inherited changes in genes may be associated with pancreatic cancer. Second, we would like to learn more about patient experiences with genetic testing, such as patient understanding of the testing, health-related actions taken (or planned to take) as a result of testing, communication and action of family members based on test results, and psychological impact of testing. This research study involves allowing collection of tumor tissue (from a prior biopsy and/or surgery), a blood sample, and sending surveys to participants for their opinion on the impact of the genetic testing as well as clinicians for relevant baseline and medical history information.

Key facts

Study ID

NCT05380557

Run by

Invitae Corporation

People needed

2

Starts

2021-08-23

Expected to finish

2022-09-06

Last updated by the study team

2022-12-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient has consented to germline genetic testing
• Patient has a histologically confirmed diagnosis of pancreatic cancer
• Patient has undergone or is planned to undergo surgical resection with curative intent
• Patient is willing to allow collection of a tissue sample from surgical resection
• Patient is willing to provide research blood samples (every 6 months for 2 years)
• Patient must be at least 18 years of age

You may not qualify if…

• Patient has evidence of metastatic or recurrent pancreatic cancer at time of consent
• Patient is unable to consent.

Where it is running

• Invitae SF — San Francisco, California, United States

Full record on ClinicalTrials.gov

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