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

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

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05380557
Acronym
ARTEMIS
Enrollment
2
Registered
2022-05-19
Start date
2021-08-23
Completion date
2022-09-06
Last updated
2022-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Adenocarcinoma, Pancreatic Cancer, Resectable Pancreatic Cancer

Keywords

germline genetic testing, oncology, pancreatic cancer, resectable pancreatic cancer, early stage pancreatic cancer

Brief summary

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.

Detailed description

Patients will be contacted for patient outcomes survey completion at months: 1, 4, 8, 12, 18, 24, 30, 36, 42, 48, 54, and 60. Patients will also be contacted for survival collection every 6 months during years 3-5 post germline testing. Clinicians will be contacted for relevant medical history, treatment, and survival data at the same time points. At baseline, 3 samples types will be collected: 1. EDTA tube for germline genetic testing. 2. Streck tubes for whole genome sequencing and other analyses. 3. Tumor block from surgical resection. If block is unavailable 10 unstained slides are an acceptable substitute.

Interventions

DIAGNOSTIC_TESTGermline genetic testing

Germline genetic testing will be provided to each patient

Sponsors

Eastern Cooperative Oncology Group
CollaboratorNETWORK
Invitae Corporation
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Germline pathogenic variants identified on Invitae's 84 gene Multi Cancer panelWill be assessed at baseline only.
Overall survivalWill be assessed in patient and clinician surveys distributed every 4 months for the first year post germline testing

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026