Sentinel™ Trial: A Prospective Study Evaluating the Performance and Clinical Benefit of Personalized ctDNA-based MRD Testing to Detect Recurrence and Monitor Treatment Response in Patients With Solid Tumors

Launched by STRATA ONCOLOGY · Oct 5, 2021

Keywords

ClinConnect Summary

Patients with a confirmed diagnosis of a stage I through III solid tumor who have had definitive therapy or curative surgery within the last 5 years or are planning curative surgery may be eligible for the Sentinel Trial. Patients must have a surplus formalin-fixed paraffin-embedded tumor specimen available at screening, or a planned resection within 28 days of screening. To support ctDNA assessment, study procedures will be limited to serial blood draws repeated every 12 weeks until investigator determined recurrence. Upon recurrence, participants will remain on study for 3 years in surviv...

Gender

ALL

Eligibility criteria

• Study participants must meet all the inclusion criteria below to enroll:
• • 1. Male or female participants ≥ 18 years of age;
• • 2. Confirmed diagnosis of a stage 1-3 solid tumor;
• • 3. Curative surgery or definitive therapy (e.g., chemoradiation, stereotactic body radiation therapy \[SBRT\]) completed \<5 years ago without any current evidence of radiographical or biochemical recurrence, or planned within 28 days of consent;
• • 4. Surplus formalin fixed paraffin embedded tumor specimen available;
• • 5. Able to tolerate venipuncture for blood draws;
• • 6. Primary diagnosis is not glioma or CNS disease;
• • 7. Both the tumor tissue sample and blood sample pass the quantity and quality parameters to allow for a successful MRD test result.