About this trial
Earlier detection of disease recurrence will enable greater treatment options and has strong potential to improve patient outcomes. This project is translational and has the potential to lead to future translational research opportunities, including interventional trials in which therapeutic escalation is offered at the early circulating tumor DNA (ctDNA) molecular residual disease (MRD) detection timepoint. Ultimately, the integration of ctDNA into the clinical workflow has the potential to enhance cancer diagnosis, treatment, surveillance, and prognosis, and guide clinical decision-making in this era of personalized precision medicine.
Eligibility criteria
Qualifiers
Eligible healthy donors will be at least 18 years of age.
Disqualifiers
Healthy donors younger than 18 years of age
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Washington University School of Medicine
Lead sponsor
Roche Sequencing Solutions
Collaborator
The Foundation for Barnes-Jewish Hospital
Collaborator
National Center for Advancing Translational Sciences (NCATS)
Collaborator
Radiological Society of North America
Collaborator
Skandalaris
Collaborator
The V Foundation for Cancer Research
Collaborator
National Institute of General Medical Sciences (NIGMS)
Collaborator