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This study investigates the value of circulating tumor DNA (ctDNA) in the blood for predicting disease course after the first 6 months of treatment in patients with Waldenström macroglobulinemia. It enrolls patients who meet the diagnostic criteria and require first-line or subsequent-line therapy. It is conducted as a study without a phase designation and is currently recruiting participants.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * Patient with WM according to diagnostic criteria * Patients with WM followed in one of the centre of North-Western region. * Patients requiring first-line or subsequent-line therapy * Patients agreement for giving informed consent. * Social insurance system affiliation Exclusion Criteria: * Patients with another chronic B-cell malignancy * patients with other lymphoplasmacytic proliferations * patients with marginal zone lymphoma. * Patients with WM and histologic transformation * Absence of informed consent