
Dr Linscott on the Need for Improved MRD Detection in High-Risk NMIBC
Joshua Linscott, MD, PhD, discusses a study evaluating a utDNA assay for minimal residual disease detection in patients with high-risk NMIBC.
Joshua Linscott, MD, PhD, urologic oncology fellow, Moffitt Cancer Center, discusses the rationale for a study evaluating a urinary cell-free tumor DNA (utDNA) assay for minimal residual disease (MRD) detection in patients with high-risk non–muscle-invasive bladder cancer (NMIBC).
Patients with high-risk, NMIBC frequently experience disease recurrence, although progression to muscle-invasive disease is relatively uncommon, Linscott begins. Current recurrence surveillance strategies involve invasive procedures, primarily cystoscopy, conducted every 3 to 6 months until a recurrence occurs, he notes. These monitoring strategies underscore the need for more efficient and less invasive diagnostic tools that can accurately detect disease recurrence and assess the risk of progression, Linscott emphasizes. Additionally, there is a pressing need to identify predictive biomarkers that can guide treatment decisions and personalize therapeutic approaches for this population, he says. Understanding which patients are at risk of progression can inform clinical decision-making, allowing for more personalized treatment approaches, Linscott explains.
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This study aimed to determine the accuracy and reliability of noninvasive testing for detecting residual disease in this population. Investigators hypothesized that success in this population would validate the test’s utility in identifying MRD and support its potential application for detecting early recurrence in patients with NMIBC, Linscott says.



































