About this trial
This study aims to evaluate the long-term efficacy of BTK inhibitor Zanubrutinib combined bendamustine and rituximab (ZBR) for time-limited treatment of Waldenstrom macroglobulinemia, The combination therapy is expected to improve the remission depth, prolong the remission time, and improve the progression-free survival and overall survival of newly diagnosed WM patients. On the one hand, the patients have to bear a long-term economic burden, which is often difficult for some patients to adhere to for a long time. On the other hand, in the course of long-term treatment of BTKi, drug resistance and intolerable side effects are prone to occur. At the same time, it can prevent the disease rebound after the withdrawal of BTKi, so as to achieve the phased withdrawal of WM
Eligibility criteria
Qualifiers
The gender of the patient is not limited, and the age is ≥18 years old;
Must meet WM's diagnostic standards;
The patient is an untreated or patient who has not undergone standard treatment.
No combined chemotherapy with BTKi, BR, RCD, VRD, CHOP and COP
Disqualifiers
Malignant tumors (including active central nervous system lymphoma) other than B-NHL have been diagnosed or treated within the past year;
There is clinical evidence that large cell lymphoma transformation has occurred;
Non-lymphoma-related liver and kidney damage: alanine aminotransferase (ALT)> 3 times the upper limit of normal value, aspartate aminotransferase (AST)> 3 times the upper limit of normal value, total bilirubin (TBIL)> upper limit of normal value 2 Times, serum creatinine clearance rate <30ml/min;
Other serious medical conditions will affect the study (such as uncontrolled diabetes, gastric ulcers, other serious cardiopulmonary diseases, etc.). The decision-making power belongs to the researcher;
Trial design
Treatments tested in this trial
- Zanubrutinib, Bendamustine and Rituximab