A Study of DNA Markers for the Detection of Metastatic Melanoma in Blood
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 18-000031
Sponsor Protocol Number: 18-000031
About this study
The purpose of this study is to discover and validate DNA methylation-based markers that identify patients with metastatic melanoma based on the detection of such markers in patient blood with the ultimate goal of using blood-based multi-marker testing as a method of disease surveillance in melanoma patients.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Eligibility will be determined based on clinicopathologic data derived from patient medical records and established by two or more board-certified Mayo Clinic pathologists.
Inclusion Criteria:
CASES and CONTROLS
CASES
Exclusion Criteria:
CASES and CONTROLS
- History of an internal malignancy other than melanoma or non-melanoma skin cancer within 5 years prior to blood draw.
- Ambiguous pathology.
- Insufficient or poor quality DNA retrievable from blood sample.
CASES
- Excluded if:
- all metastatic lesion(s) surgically removed
- exposed to radiation therapy 7 days prior to blood draw,
- transplant prior to blood draw iv) surgery or biopsy of any lesion in the 7 days prior to blood draw.
CONTROLS:
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
More information
Publications
Publications are currently not available