Zanubrutinib, Ixazomib and Dexamethasone in Patients With Treatment Naive Waldenstrom's Macroglobulinemia
A Phase 2 Clinical Trial to Evaluate the Efficacy of Zanubrutinib Plus Ixazomib and Dexamethasone in Newly Diagnosed Symptomatic Waldenström Macroglobulinemia
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 2
Contacts and Locations
Study Contact
Study Contact
- Name: Shuhua Yi, Dr
- Phone Number: 86-22-23909106
- Email: yishuhua@ihcams.ac.cn
Study Contact Backup
- Name: Lugui Qiu, Dr
- Phone Number: 86-22-23909172
- Email: qiulg@ihcams.ac.cn
Study Locations
-
-
Tianjin Municipality
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Tianjin, Tianjin Municipality, China, 300020
- Institute of Hematology & Blood Diseases Hospital
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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. The specific conditions are as follows:
- No combined chemotherapy with BR, RCD, VRD, CHOP and COP
- No treatment regimen containing fludarabine
- Chlorambucil or cyclophosphamide for less than 4 weeks (alone or in combination with adrenal glucocorticoids)
- The above treatment did not reach the treatment response (MR)
- If the above treatment has been applied, the treatment needs to be stopped for 2 weeks before entering the group to start treatment
The indications for the treatment of indolent lymphoma mainly include (at least one of the following conditions):
- Symptomatic hyperviscosity;
- symptomatic peripheral neuropathy;
- Amyloidosis;
- Cold agglutinin disease; cryoglobulinemia;
- Disease-related cytopenia (Hb<100 g/L, PLT<100×10^9/L);
- giant lymph nodes;
- Those with systemic systemic symptoms: for two weeks/recurrent fever (above 38℃) and not caused by infection, or Night sweats and/or weight loss >10% within 6 months;
- The disease progresses rapidly, for example, the lymph nodes increase by more than 50% within 2 months, and/or peripheral blood lymphocytes absolute value doubling time <6 months, and/or rapid hemoglobin or platelet non-autoimmune causes slow down
- When there is evidence that the disease has transformed.
- ECOG score ≤ 2 points
- Laboratory examination: neutrophils ≥ 0.75×10^9/L; platelets ≥ 50×10^9/L; total bilirubin ≤ 2.5 times upper limit; alanine aminotransferase/aspartate aminotransferase ≤3 times upper limit. Creatinine clearance rate ≥ 30ml/min.
- The patient's expected survival time is ≥ 3 months.
Exclusion Criteria:
- 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;
- Known history of infection with human immunodeficiency virus (HIV) or active hepatitis B virus (HBV) infection, or any uncontrolled active systemic infection requiring intravenous antibiotics.
- Central nervous system dysfunction with clinical manifestations or central invasion (Bing-Neel syndrome);
- Patients who have undergone major surgery (not including lymph node biopsy) within the past 14 days or expected major surgery during treatment;
- Inability to swallow capsules or suffer from malabsorption syndrome, diseases that significantly affect gastrointestinal function, have undergone gastric or small bowel resection, symptomatic inflammatory bowel disease or ulcerative colitis, partial or complete intestinal obstruction.
- Need to receive strong cytochrome P450 (CYP) 3A inhibitor treatment.
- Women who are pregnant or breastfeeding, women of childbearing age who have not taken contraception;
- Allergy to the drugs used.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: ZID regimen
Zanubrutinib, 160mg orally, twice a day; Ixazomib, 4 mg orally, day 1, 8, 15; Dexamethasone, 20mg orally, days 1, 8, 15.
|
Zanubrutinib, 160mg orally, twice a day; Ixazomib, 4 mg orally, day 1, 8, 15; Dexamethasone, 20mg orally, days 1, 8, 15;Ixazomib and dexamethasone every 4 weeks of a cycle, with induction of 6 cycles, and then maintain every 12 weeks, up to 6 cycles (96 cycles in total).
Zanubrutinib is taken orally twice a day for up to 96 cycles, with a reduction in the last ID cycle.
ZID regimen will continue 6 cycles after reaching the maximum response after introduction section.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deep remission response rate
Time Frame: up to 5 years
|
≥VGPR after 6 cycles introduction
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up to 5 years
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Complete response (CR)
Time Frame: up to 12 months
|
Disappearance of monoclonal protein on immunofixation (both serum and urine); No histologic evidence of bone marrow involvement; Resolution of adenopathy and/or organomegaly on CT; Resolution of clinical signs or symptoms attributed to WM/LPL.
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up to 12 months
|
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Progress-free survival (PFS)
Time Frame: up to 5 years
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the time from treatment initiation until disease progression or death
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up to 5 years
|
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Duration of response (DoR)
Time Frame: up to 5 years
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the time from best response (R) to progression/death (P/D)
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up to 5 years
|
|
Overall survival (OS)
Time Frame: up to 36 months
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The percentage of patients in treatment group who are still alive for a certain period of time after they were diagnosed with Waldenstrom's Macroglobulinemia.
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up to 36 months
|
|
Time to next treatment (TTNT)
Time Frame: up to 5 years
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time from end of primary treatment to institution of next therapy
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up to 5 years
|
|
Overall response
Time Frame: up to 5 year
|
minimor response+partial response+VGPR+CR
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up to 5 year
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Shuhua Yi, Chinese Academy of Medical Sciences and Peking Union Medical College
Publications and helpful links
General Publications
- Treon SP, Xu L, Guerrera ML, Jimenez C, Hunter ZR, Liu X, Demos M, Gustine J, Chan G, Munshi M, Tsakmaklis N, Chen JG, Kofides A, Sklavenitis-Pistofidis R, Bustoros M, Keezer A, Meid K, Patterson CJ, Sacco A, Roccaro A, Branagan AR, Yang G, Ghobrial IM, Castillo JJ. Genomic Landscape of Waldenstrom Macroglobulinemia and Its Impact on Treatment Strategies. J Clin Oncol. 2020 Apr 10;38(11):1198-1208. doi: 10.1200/JCO.19.02314. Epub 2020 Feb 21.
- Treon SP, Xu L, Hunter Z. MYD88 Mutations and Response to Ibrutinib in Waldenstrom's Macroglobulinemia. N Engl J Med. 2015 Aug 6;373(6):584-6. doi: 10.1056/NEJMc1506192. No abstract available.
- Castillo JJ, Meid K, Gustine JN, Dubeau T, Severns P, Hunter ZR, Yang G, Xu L, Treon SP. Prospective Clinical Trial of Ixazomib, Dexamethasone, and Rituximab as Primary Therapy in Waldenstrom Macroglobulinemia. Clin Cancer Res. 2018 Jul 15;24(14):3247-3252. doi: 10.1158/1078-0432.CCR-18-0152. Epub 2018 Apr 16.
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Vascular Diseases
- Cardiovascular Diseases
- Neoplasms
- Immune System Diseases
- Neoplasms by Histologic Type
- Hematologic Diseases
- Lymphatic Diseases
- Lymphoproliferative Disorders
- Immunoproliferative Disorders
- Neoplasms, Plasma Cell
- Hemostatic Disorders
- Paraproteinemias
- Blood Protein Disorders
- Hemorrhagic Disorders
- Hemic and Lymphatic Diseases
- Waldenstrom Macroglobulinemia
- Polycyclic Compounds
- Pregnadienes
- Pregnanes
- Steroids
- Fused-Ring Compounds
- Steroids, Fluorinated
- Pregnadienetriols
- Dexamethasone
- zanubrutinib
- ixazomib
Other Study ID Numbers
Other Study ID Numbers
- IIT2020002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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