Zanubrutinib Combined With BR in the First-line Treatment of Waldenström's Macroglobulinemia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorPeking Union Medical College Hospital

About this trial

Current retrospective studies have demonstrated that achieving deep remission following treatment for Waldenström's macroglobulinemia (WM) correlates with prolonged survival. While the bendamustine-rituximab (BR) regimen or single-agent zanubrutinib are currently recommended as first-line therapies, neither achieves optimal deep remission. Additionally, prolonged zanubrutinib monotherapy may lead to cumulative adverse effects. Therefore, this study aims to evaluate the efficacy and safety of the bendamustine-rituximab-zanubrutinib combination regimen as a first-line treatment option for MYD88-mutated WM patients.

Eligibility criteria

Qualifiers

Presence of monoclonal IgM-type immunoglobulin in serum

Bone marrow infiltration by plasmacytoid lymphocytes or bone marrow biopsy showing small lymphocytes/plasma cells/plasmacytoid lymphocytes (any quantity) in the intertrabecular space

Exclusion of other non-Hodgkin lymphoma subtypes

Typical immunophenotype: CD5-/CD10-/CD19⁺/CD20⁺/CD23-/CD79b⁺ /sIgM⁺/CD138- clonal B-cells. Variant phenotypes may show CD5/CD10/CD23 /CD38 positivity or coexistence of clonal B-cells and plasma cells.

Disqualifiers

Co-morbidity of uncontrolled infection or autoimmune disease

Co-morbidity of other active malignancy

Co-morbidity of uncontrolled heart disease

Co-morbidity of severe digestive system disorders precluding oral medication

Trial design

Treatments tested in this trial

  • Zanubrutinib
  • Bendamustine + Rituximab

Treatment groups

104 Participants
are divided into 1 treatment group