Trial of ctDNA of Guidance to Determine PostOperative Radiation Therapy

EARLY_PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

June 1, 2025

Primary Completion Date

June 1, 2028

Study Completion Date

June 1, 2029

Conditions
Lung CancerNon Small Cell Lung CancerLung Cancer Recurrent
Interventions
DIAGNOSTIC_TEST

Haystack™ ctDNA Assay

A personalized, tumor-informed circulating tumor DNA (ctDNA) test that analyzes blood samples to detect minimal residual disease (MRD) and guide postoperative treatment decisions for patients with Stage II-III non-small cell lung cancer (NSCLC) following surgical resection. The test results will help determine whether patients should receive postoperative radiation therapy (PORT) and/or systemic therapy adjustments.

Trial Locations (1)

08901

Rutgers Cancer Institute, New Brunswick

All Listed Sponsors
lead

Rutgers, The State University of New Jersey

OTHER