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Response assessment after frontline therapy for large B-cell lymphoma risk-stratifies patients into those at low risk for relapse and those with residual disease. Positron emission tomography scans form the cornerstone of the response criteria but cannot detect molecular-only disease. Circulating tumor DNA detects measurable residual disease (MRD) after therapy which is emerging as an adjunct tool for complex clinical decision-making. We discuss how MRD after therapy can be clinically implemented and additional data needed to unlock its full potential.
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Merryman et al. (2026) studied this question.
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