Study of Zanubrutinib, Obinutuzumab, and Venetoclax in Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Leukemia (SLL)

Chronic Lymphocytic Leukemia (CLL) Clinical Trial

Official title:

Phase 2 Study of Zanubrutinib, Obinutuzumab, and Venetoclax in Previously Untreated Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) and Mantle Cell Lymphoma (MCL)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03824483
• Other study ID #: 18-427
• Status: Recruiting
• Phase: Phase 2
• Start date: February 22, 2019
• Est. completion date: February 2025

Study information

• Verified date: June 2024
• Source: Memorial Sloan Kettering Cancer Center
• Contact: Andrew Zelenetz, MD, PhD
• Phone: 212-639-2656
• Email: zeleneta[@]mskcc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the rate of minimum residual disease (MRD) negative response (i.e. the rate of no evidence of disease) of the study drugs, zanubrutinib, obinutuzumab, and venetoclax, given in combination as a treatment for CLL and/or SLL.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 230
• Est. completion date: February 2025
• Est. primary completion date: February 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed, informed consent

• Ability and willingness to comply with the requirements of the study protocol

• Age =18 years

• Diagnosis of the following histories according to the WHO criteria

1. CLL or SLL

2. MCL

• For patients with SLL, peripheral blood flow cytometry must be positive with CLL-like cells accounting for at least 1% of circulating WBC.

• No prior systemic therapy for disease under study except:

1. prior local radiation for symptomatic disease is permitted

2. Short course systemic corticosteroids is permissible for disease control, improvement of performance status or non-cancer indication (must be = 14 days and < 100 mg/day prednisone or = 20 mg/day dexamethasone). Steroids must be discontinued prior to study treatment. Inhaled steroids for asthma, topical steroids, and replacement/Stress corticosteroids are permitted. Low-dose steroids for ITP are also permitted up to the equivalent prednisone 20mg/daily at time of eligibility review.

• ECOG performance status of 0 to 2

• Adequate hematologic parameters unless due to disease under study:

1. Absolute neutrophil count (ANC) =1.0 x 109/L unless neutropenia is clearly due to disease under study (per investigator discretion)

2. Platelet count = 75,000/mm3 - OR - Platelet count = 20,000/mm3 if thrombocytopenia is clearly due to disease under study (per investigator discretion)

3. Hemoglobin =9.0 g/dL unless anemia is clearly due to marrow involvement due to disease under study (per investigator discretion)

• Adequate renal and hepatic function, per laboratory reference range at Screening as follows:

a. AST/SGOT, ALT/SGPT =2.0 x ULN b. Total bilirubin = 2.0 x ULN unless:

i. Considered secondary to Gilbert"s syndrome, in which case =3 x ULN ii. Considered due to disease under study (Per PI or Co-PI discretion)

c. Creatinine clearance of eGFR>30 mL/min according to the Cockcroft-Gault Equation

• For females of childbearing potential, a negative serum pregnancy test within 7 days of study treatment

• For female patients of childbearing potential, agreement to use highly effective form(s) of contraception (i.e., one that results in a low failure rate [<1% per year] when used consistently and correctly) or remain abstinent (refrain from heterosexual intercourse) during the treatment period and to continue its use for 90 days after the last dose of zanubrutinib AND 30 days after the last dose of venetoclax AND for 18 months after the last dose of obinutuzumab (whichever date is later)

A woman is considered to be of childbearing potential if she is postmenarcheal, has not reached a postmenopausal state (>/= 12 continuous months of amenorrhea with no identified cause other than menopause), and it not permanently infertile due to surgery (i.e., removal of ovaries, fallopian tubes, and/or uterus) or another cause as determined by the investigator (e.g., Mullerian agenesis). The definition of childbearing potential may be adapted for alignment with local guidelines or regulations.

Examples of contraceptive methods with a failure rate of <1% per year include bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices. Hormonal contraceptive methods must be supplemented by a barrier method.

1. The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.

• For men with a female partner of childbearing potential or a pregnant female partnet: agreement to remain abstinent (refrain from heterosexual intercourse) or use a condom during the treatment period and to continue its use for 90 days after the last dose of zanubrutinib, or venetoclax AND for 18 months after the last dose of obinutuzumab (whichever date is later)

The reliability of sexual abstinence should be evaluated in relation duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception - Willingness to not donate or bank sperm or oocytes during the entire study treatment period and after treatment discontinuation for 90 days after the last dose of zanubrutinib AND 30 days after the last dose of venetoclax AND for 18 months after the last dose of obinutuzumab (whichever date is later)

Additional Eligibility Criteria for CLL Cohort:

1. Diagnosis of untreated CLL or SLL according to WHO criteria 2. For patients with SLL, peripheral blood flow cytometry must be positive with CLL-like cells accounting for at least 1% of circulating WBC 3. No prior systemic therapy for CLL: prior single site of local radiation for symptomatic disease is permitted 4. Subject requires treatment according to IWCLL guidelines (See Appendix A)

Additional Eligibility Criteria for TP53 Mutant MCL cohorts:

1. Diagnosis of untreated stage II-IV mantle cell lymphoma

a. Prior radiotherapy for localized disease is permitted 2. Presence of TP53 mutation irrespective of variant allele frequency (TP53 cohort)

OR

Presence of p53 overexpression by immunohistochemistry defined as strong nuclear staining of >30% positive nuclei.

Additional Eligibility Criteria for Transplant Ineligible MCL cohort:

1. Diagnosis of untreated stage II-IV mantle cell lymphoma

a. Prior radiotherapy for localized disease is permitted

2. Patients must meet one of the following criteria (a or b):

1. Age =65 years If age <65 years of age, then patients must be ineligible for HDT/ASCT on the basis of comorbidity or organ dysfunction.

Specifically, patients must meet at least one of the following criteria below:

i.. Comorbid disease, such as CAD, CHF, pulmonary dysfunction, liver or kidney dysfunction, precluding high dose therapy secondary to expected increased morbidity and mortality. ii. ECOG 2 iii. Ejection fraction =35% and <45% iv. Impaired pulmonary function test with DLCO <50% expected v. Medical conditions which in the opinion of the treating physician in consultation with the study PI or Co-PI and DMT preclude HDT/ASCT.

Exclusion Criteria:

Other malignancies:

• Known active histological transformation from CLL to an aggressive lymphoma (i.e., Richter"s transformation)

• Active malignancy or systemic therapy for another malignancy within 3 years; local/regional therapy with curative intent such as surgical resection or localized radiation within 3 years of treatment is permitted

• Other diagnosis of active cancer

Co-morbidities:

• Any uncontrolled illness that in the opinion of the investigator would preclude administration of study therapy (e.g. significant active infections, hypertension, angina, arrhythmias, pulmonary disease, or autoimmune dysfunction)

• Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment, or any major episode of infection requiring treatment with IV antibiotics or hospitalization (relating to the completion of the course of antibiotics) within 4 weeks prior to Cycle 1, Day 1

• Known bleeding diathesis

• Prior major surgical procedure within 4 weeks of study, or anticipation of need for a major surgical procedure during the course of the study

• Known CNS hemorrhage or stroke within 6 months of the study

• History of progressive multifocal leukoencephalopathy (PML)

• History of HIV infection or active hepatitis B (chronic or acute) or hepatitis C infection

a. Patients with occult or prior HBV infection (defined as positive total hepatitis B core antibody [HBcAb] and negative HBsAg) may be included if HBV DNA is undetectable. These patients must be willing to take appropriate anti-viral prophylaxis as indicated and undergo monthly DNA testing.

b. Patients positive for hepatitis C virus (HCV) antibody are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA

• Congestive heart failure, New York Heart Association classification III/IV

• Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis

• Receipt of live-virus vaccines within 28 days prior to the initiation of study treatment or need for live-virus vaccines at any time during study treatment

• Known condition or other clinical situation that would affect oral absorption

• Psychiatric illness/social situations that would interfere with study compliance

• Inability to swallow a large number of tablets

Concomitant medications and drug interactions:

• Administration within 7 days prior to the first dose of study drug or concurrent therapy with strong inhibitors or inducers of CYP3A, CYP2C8, CYP2C9 and CYP2C19. The same applied for moderate inhibitors or inducers of CY_3A

• Live-virus vaccines given within 28 days prior to the initiation of study treatment

• Immunotherapy

• Hormone therapy (other than contraceptives, hormone replacement therapy, or megestrol acetate)

• Any therapies intended for the treatment of lymphoma/leukemia whether FDA approved or experimental (outside of this study)

• Radiation therapy intended to treat MCL or CLL/SLL

• Warfarin or warfarin derivatives

• Consumption of one or more of the following within 3 days prior to the first dose of study drug:

Grapefruit or grapefruit products Seville oranges, including marmalade containing Seville oranges Star Fruit (carambola)

Prior therapy:

• Prior anti-CD20 monoclonal antibody therapy for non-malignant indication

• Obinutuzumab is contraindicated in patients with a known hypersensitivity (IgE-mediated) reaction to obinutuzumab or to any of its excipients

• Prior systemic therapy for CLL; prior single site of local radiation for symptomatic disease is permitted

Other:

• Females who are currently pregnant or breastfeeding

• Participation in a separate investigational therapeutic study unless authorized by the investigator

Related Conditions & MeSH terms

• Chronic Lymphocytic Leukemia (CLL)
• Leukemia
• Leukemia, Lymphocytic, Chronic, B-Cell
• Leukemia, Lymphoid
• Small Lymphocytic Leukemia (SLL)

Intervention

Drug:
• Zanubrutinib
zanubrutinib (160mg by mouth BID)
• Obinutuzumab
obinutuzumab (1000mg IVPB on Days 1*, 8 and 15 of Cycle 1 and on Day 1 of Cycles 2 through 8) starting on Cycle 1 (28-day cycles). * On Cycle 1, obinituzumab will be administered in "split dose" at 100mg IVPB on Day 1 and 900mg IVPB on Day 2 in patients at increased risk for IRR (ALC >25,000 cells/ul or baseline lymph nodes >5 cm diameter).
• Venetoclax
Venetoclax will be added to the regimen starting on Cycle 3, and will be incorporated into the regimen using the 5-week ramp-up schedule to mitigate the risk of tumor lysis syndrome (beginning at 20mg and gradually increasing to 400mg), and venetoclax will be administered a ta fixed dose level of 400mg by mouth daily of 28-day cycles thereafter.

Locations

Country	Name	City	State
United States	Memorial Sloan Kettering at Basking Ridge	Basking Ridge	New Jersey
United States	Massachusetts General Hospital (Data Collection and Specimen Analysis)	Boston	Massachusetts
United States	Memorial Sloan Kettering Commack	Commack	New York
United States	Northwestern University	Evanston	Illinois
United States	Memorial Sloan Kettering Westchester	Harrison	New York
United States	Memorial Sloan Kettering Monmouth	Middletown	New Jersey
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	Memorial Sloan Kettering Nassau	Uniondale	New York

Sponsors (4)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center	BeiGene USA, Inc., Massachusetts General Hospital, Roche-Genentech

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	establish the rate of minimum residual disease (MRD) undetectable response	Patients will have their minimum residual disease (MRD) response classified by bone marrow peripheral blood flow cytometry with a sensitivity of 10-4.	1 year

External Links

•   Memorial Sloan Kettering Cancer Center