A Single Arm Phase I/II Study of Tazemetostat with Rituximab and Abbreviated Bendamustine in the Frontline Treatment of High Tumor Burden Follicular Lymphoma.
Primary Objectives:
Phase I: To evaluate the safety and tolerability of tazemetostat in combination with bendamustine and rituximab.
Phase II: To assess the complete metabolic response CMR rate in patients treated with 3 cycles of BR plus tazemetostat followed by 3 cycles of rituximab plus tazemetostat.
Secondary Objectives:
- To estimate the ORR and CMR rate after 3 cycles of BR plus tazemetostat.
- To evaluate the duration of response of tazemetostat in combination with bendamustine and rituximab.
Exploratory Objectives:
- To estimate the PFS and OS at 2 years post completion of treatment.
- To evaluate the minimal residual disease (MRD) rate throughout study treatment.
- To evaluate EZH2 mutation status and response by mutational status.
Tazemetostat
RITUXIMAB
- Rutgers Cancer Institute of New Jersey
- RWJBarnabas Health
- Community Medical Center
- Monmouth Medical Center
Inclusion Criteria
- Written informed consent and HIPAA authorization for release of personal health
information. NOTE: HIPAA authorization may be included in the informed consent or
obtained separately.
- Age ≥ 18 years at the time of consent.
- ECOG Performance Status of 0-2 within 10 days prior to registration.
- Low grade follicular lymphoma (grade 1-2 or 3A by WHO-HAEM4R and/or cFL by WHO-HAEM5).
Specifically, grade 3B or FLBL will not be allowed. Must not have evidence of
transformed lymphoma at the time of study enrollment.
- Stage II, III, or IV by Ann Arbor staging system.
- Meet the definition of high tumor burden follicular lymphoma as defined by Groupe
d'Etude des Lymphomes Follicularies (GELF) Criteria or be defined as high risk by the
follicular lymphoma international prognostic index (FLIPI) 1 or FLIPI 2.
--GELF Criteria (Must meet ≥ 1 of the following)
- Any nodal or extranodal mass ≥ 7 cm in diameter
- Involvement of ≥ 3 nodal sites ≥ 3 cm
- Systemic or B symptoms
- Presence of serous effusion
- Splenic enlargement
- Risk of compression syndrome (epidural, ureteral, etc)
- Leukemic phase of disease
- Cytopenia deemed due to disease involvement (hemoglobin < 10, granulocyte count <
1.5×10^9/L, or platelet count < 100×10^9/L)
- In addition to meeting GELF criteria, must have at least one FDG-avid site on PET that
measures 1.5 cm in at least one dimension of a nodal site or 1cm in at least one
dimension for extranodal sites.
- Received no prior therapy except local radiation therapy (field did not exceed 2
adjacent nodal regions), single agent rituximab (limited to 4 doses), or steroids for
symptom control in the 28 days preceding trial enrollment.
- Must have prior EZH2 testing already performed or have tissue available to perform
retrospective EZH2 testing. If prior EZH2 results are not available, tissue must be
submitted. Tissue block is preferred but unstained slides are also acceptable.
Patients who have insufficient or suboptimal tissue must be willing to have a biopsy
performed prior to starting study drugs. See Correlative Lab Manual for details.
- Demonstrate adequate organ function as defined below; all screening labs to be
obtained within 28 days prior to registration.
- Hematological
- Platelets ≥ 50 K/dL
- Absolute Neutrophil Count (ANC) ≥ 1000 K/mm3
- Hemoglobin (Hgb) ≥ 8 g/dL
- Renal
- Calculated creatinine clearance ≥ 40 mL/min using the Cockcroft-Gault
formula
- or Serum creatinine < 2 mg/dL
- Hepatic
- Bilirubin ≤ 1.5 × upper limit of normal (ULN)
- Aspartate aminotransferase (AST) ≤ 3 × ULN
- Alanine aminotransferase (ALT) ≤ 3 × ULN
- Coagulation ---International Normalized Ratio (INR) or Prothrombin Time (PT)
Activated Partial Thromboplastin Time (aPTT) ≤ 2 × ULN
- Females of childbearing potential with a male partner able to father a child must have
a negative serum or urine pregnancy test within 7 days prior to registration. See the
protocol for definition of childbearing potential.
- Females of childbearing potential must be willing to abstain from vaginal intercourse
or use an effective method(s) of contraception from the time of informed consent,
during the study and for 6 months after the last dose of study drug(s). Males able to
father a child must be willing to abstain from vaginal intercourse or to use an
effective method(s) of contraception from initiation of treatment, during the study
and for 3 months after the last dose of study drug(s). See the protocol.
- As determined by the enrolling physician or protocol designee, ability of the subject
to understand and comply with study procedures for the entire length of the study.
Exclusion Criteria
- Active infection requiring systemic therapy with 4 weeks of study drug administration.
- Pregnant or breastfeeding (NOTE: breast milk cannot be stored for future use while the
mother is being treated on study).
- Concurrent malignancy or malignancy within the last 3 years (except for ductal breast
cancer in situ, non-melanoma skin cancer, prostate cancer not requiring treatment, and
cervical carcinoma in situ) whose natural history or treatment has the potential to
interfere with the safety or efficacy assessment of the investigational regimen are
not eligible for this trial.
- Active central nervous system (CNS) metastases or leptomeningeal disease. NOTE:
Subjects who are symptomatic and have not undergone prior brain imaging must undergo a
head computed tomography (CT) scan or brain MRI within 28 days prior to registration
to exclude brain metastases.
- Treatment with any investigational drug within 4 weeks prior to registration.
- Subjects who require chronic use of moderate or strong CYP3A4/5 inhibitors or inducers
within 28 days prior to registration.
- Clinically significant acute infection requiring systemic antibacterial, antifungal,
or antiviral therapy.
- Known Uncontrolled Human Immunodeficiency Virus infection. Testing not required. NOTE:
If a subject is known to have HIV/AIDS, then they will be allowed on study with
adequate antiviral therapy, no detectable viral load, and stable on antiviral
treatment for ≥ 4 weeks prior to first dose of study drug(s).
- Known hepatitis C infection. Testing not required. NOTE: If hepatitis C antibody test
is known positive, patients are excluded unless a hepatitis C virus ribonucleic acid
(HCV RNA) is negative.
- Must be tested for hepatitis B within 28 days of registration: including hepatitis B
surface antigen, hepatitis B surface antibody, hepatitis B core antibody. A positive
hepatitis B core antibody should be followed by hepatitis B DNA PCR testing to confirm
or rule out active infection. Patients with hepatitis B surface antigen and/or
detectable hepatitis B DNA PCR are not allowed on study. Patients with a positive
hepatitis B core antibody but negative hepatitis B surface antigen and hepatitis B DNA
PCR will be allowed on study, but hepatitis B prophylactic treatment should be
strongly considered.
- Clinically significant cardiovascular disease or cardiac insufficiency (New York Heart
Association classes III-IV), cardiomyopathy, preexisting clinically significant
arrhythmia, acute myocardial infarction within 3 months of enrollment, angina pectoris
within 3 months of enrollment.
Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.
For further information about clinical trials, please contact us at 732-235-7356.