Molecular Residual Disease in Solid Tumors: A Prospective Study to Collect Clinical Data and Biospecimens to Support Discovery and Development of Cancer Biomarkers
Summary
The purpose of this observational study is to collect clinical information, blood, and tumor tissue samples from participants diagnosed with stage I, stage II, or operable stage III cancer in select solid tumors. The information collected will be used to develop tests to better understand cancer, for example, to improve cancer detection and to assess the risk of cancer coming back. Participants will receive routine standard of care from their doctor and their involvement is expected to last for approximately five and a half (5.5) years.
Arms & interventions
- Diagnostic Testblood and tissue samples
routine standard of care
- Otherblood and tissue samples
Routine standard of care
Outcome measures
Primary
Blood and tissue biospecimen registry
To establish a blood and tissue biospecimen resource in participants with operable solid tumors, with clinical, lab, radiographic, and pathology annotation for the discovery, development, and validation of MRD assays.
Time frame: Observation from enrollment to 5.5 years after enrollment
Eligibility criteria
Study locations (2)
Medical Oncology Associates of San Diego
San Diego, California, 92123
Taylor Cancer Research Center
Maumee, Ohio, 43437