The goal of this clinical trial is to learn if Zanubrutinib, Rituximab, and Lenalidomide works to treat marginal zone lymphoma as the first-line therapy. It will also learn about the safety of the treatment. The main questions it aims to answer are Does the combined therapy prolong patient survival? What medical problems do participants have when using this therapeutic approach? Researchers will observe the treatment to see if it works well than conventional therapies. Participants will Administer drugs as required by the protocol Visit the clinic regularly for checkups and tests Keep a diary of their symptoms, examination and laboratory test indicators
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
This study enrolls patients with marginal zone lymphoma who require the primary treatment. Participants receive a combined therapy consisting of zanubrutinib, rituximab, and lenalidomide.
This study enrolls patients with marginal zone lymphoma who require the primary treatment. Participants receive a combined therapy consisting of zanubrutinib, rituximab, and lenalidomide.
CRR
Complete remission rate
Time frame: 2 years
ORR
Objective response rate
Time frame: 2 years
2 year-progress free survival rate
the time from the start of treatment to the time when the patient has progressed on the disease or dies due to any cause in 2 years.
Time frame: 2 years
TTR
Time from randomization to the first documentation of Complete Response (CR) or Partial Response (PR) , verified by computed tomography (CT) and positron emission tomography (PET)-CT at least 6 weeks apart
Time frame: From randomization up to 24 months post-randomization
DoR
The interval from the date of first confirmed OR to the first evidence of progressive disease or death from any cause
Time frame: From the date of first confirmed CR/PR up to 24 months post-confirmed response
OS
The time from the date of randomization to the date of death from any cause
Time frame: From randomization up to 24 months post-randomization
Incidence rate of adverse events
Time frame: 2 years
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