
Advancing Lymphoma Care: ctDNA Applications in Risk Stratification and Treatment Monitoring
Dr. Megan Melody from Tampa General Hospital Cancer Institute and Dr. Mark Roschewski from Memorial Sloan Kettering Cancer Center discussed how circulating tumor DNA (ctDNA) testing is transforming lymphoma care through enhanced risk stratification, treatment monitoring, and personalized patient management. Key insights emphasized ctDNA as an emerging risk factor superior to baseline assessments, with most patients achieving undetectable levels after 2 cycles. Combined negative positron emission tomography and ctDNA results reduce relapse risk from 15% to 20% to single digits. However, ctDNA currently serves as a prognostic marker rather than treatment-guiding tool, with ongoing ALPHA3 trial investigating ctDNA-guided therapy using allogeneic CAR-T cells. Clinical Implementation: • Seventy-five percent concordance between ctDNA and PET imaging results • Serial testing preferred over single time-point assessments for surveillance • Technology varies across lymphoma subtypes, with phased variant assays showing superior sensitivity • Quantitative values enable kinetic monitoring for individual patients with baseline controls
Advancing Lymphoma Care: ctDNA Applications in Risk Stratification and Treatment Monitoring
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Can ctDNA spot relapse early and justify treating "molecular" lymphoma? Alpha-3 tests allo CAR T, weighing toxicity, MRD clearance, survival.

Alpha-3 sparks debate on treating ctDNA-positive lymphoma early—can allo CAR T or bispecifics erase MRD without excess toxicity?

Can ctDNA and interim PET guide shorter DLBCL chemo? Experts weigh de-escalation to reduce toxicity and urge randomized trials.

Can ctDNA and interim PET guide shorter DLBCL chemo? Experts weigh de-escalation to cut toxicity, urging randomized trials.

How ctDNA trends after CAR T reshape relapse monitoring, pairing MRD blood tests with PET scans to gauge response and relapse risk.

Experts weigh ctDNA blood tests in lymphoma, highlighting phased-variant assays for end-of-therapy sensitivity and future tech advances.
