Detection of molecular residual disease (MRD) by circulating tumor DNA (ctDNA) has become an important biomarker in optimizing clinical trials and for patient management across multiple solid tumors. The Signatera MRD assay has been shown to identify high-risk patients who are likely to relapse without additional/novel treatment, underscoring a need for more interventional trials in these populations.
Join our discussion on the latest data from ASCO GI including 2024 publications validating the prognostic and predictive capabilities of ctDNA in colorectal, gastroesophageal, and pancreatic cancers.
Adham Jurdi, MD, is a Board-certified Medical Oncologist who specializes in gastrointestinal malignancies. Prior to joining Natera, Dr. Jurdi practiced at Austin Cancer Center, SUNY Upstate Medical University and the Syracuse VAMC. Throughout his clinical career, he was involved in GI oncology and precision medicine research.
John Simmons, PhD currently leads oncology biopharma partnerships at Natera. Before joining Natera, John completed his postdoctoral fellowship at the National Cancer Institute (NCI) and served as Vice President of Translational Medicine at Personal Genome Diagnostics (PGDx). He received his PhD in Tumor Biology from Georgetown University.