Principal Investigator
Enrollment Status
Clinical Trial ID
Clinical Trial Summary
This phase II Pediatric MATCH trial studies how well tazemetostat works in treating patients
with brain tumors, solid tumors, non-Hodgkin lymphoma, or histiocytic disorders that have
come back (relapsed) or do not respond to treatment (refractory) and have EZH2, SMARCB1, or
SMARCA4 gene mutations. Tazemetostat may stop the growth of tumor cells by blocking EZH2 and
its relation to some of the pathways needed for cell proliferation.
Phase
Phase 2
Funding Agency/Sponsor
National Cooperative Group
Disease
Pediatric Cancer
Enrollment Eligibility
Inclusion Criteria:
- Patient must have enrolled onto APEC1621SC and must have been given a treatment
assignment to Molecular Analysis for Therapy Choice (MATCH) to APEC1621C based on the
presence of an actionable mutation
- Patients must have radiographically measurable disease at the time of study
enrollment; patients with neuroblastoma who do not have measurable disease but have
MIBG+ evaluable disease are eligible; measurable disease in patients with CNS
involvement is defined as tumor that is measurable in two perpendicular diameters on
magnetic resonance imaging (MRI) and visible on more than one slice; Note: The
following do not qualify as measurable disease:
- Malignant fluid collections (e.g., ascites, pleural effusions)
- Bone marrow infiltration except that detected by MIBG scan for neuroblastoma
- Lesions only detected by nuclear medicine studies (e.g., bone, gallium or
positron emission tomography [PET] scans) except as noted for neuroblastoma
- Elevated tumor markers in plasma or cerebrospinal fluid (CSF)
- Previously radiated lesions that have not demonstrated clear progression post
radiation
- Leptomeningeal lesions that do not meet the measurement requirements for Response
Evaluation Criteria in Solid Tumors (RECIST) 1.1
- Karnofsky >= 50% for patients > 16 years of age and Lansky >= 50 for patients =< 16
years of age; Note: Neurologic deficits in patients with CNS tumors must have been
stable for at least 7 days prior to study enrollment; patients who are unable to walk
because of paralysis, but who are up in a wheelchair, will be considered ambulatory
for the purpose of assessing the performance score
- Patients must have fully recovered from the acute toxic effects of all prior
anti-cancer therapy and must meet the following minimum duration from prior
anti-cancer directed therapy prior to enrollment; if after the required timeframe, the
numerical eligibility criteria are met, e.g. blood count criteria, the patient is
considered to have recovered adequately
- Cytotoxic chemotherapy or other anti-cancer agents known to be myelosuppressive
- >= 21 days after the last dose of cytotoxic or myelosuppressive chemotherapy
(42 days if prior nitrosourea)
- Anti-cancer agents not known to be myelosuppressive (e.g. not associated with
reduced platelet or absolute neutrophil count [ANC] counts): >= 7 days after the
last dose of agent
- Antibodies: >= 21 days must have elapsed from infusion of last dose of antibody,
and toxicity related to prior antibody therapy must be recovered to grade =< 1
- Corticosteroids: If used to modify immune adverse events related to prior
therapy, >= 14 days must have elapsed since last dose of corticosteroid
- Hematopoietic growth factors: >= 14 days after the last dose of a long-acting
growth factor (e.g. pegfilgrastim) or 7 days for short-acting growth factor; for
growth factors that have known adverse events occurring beyond 7 days after
administration, this period must be extended beyond the time during which adverse
events are known to occur; the duration of this interval must be discussed with
the study chair and the study-assigned research coordinator
- Interleukins, interferons and cytokines (other than hematopoietic growth
factors): >= 21 days after the completion of interleukins, interferon or
cytokines (other than hematopoietic growth factors)
- Stem cell Infusions (with or without total body irradiation [TBI]):
- Allogeneic (non-autologous) bone marrow or stem cell transplant, or any stem
cell infusion including donor lymphocyte infusion (DLI) or boost infusion:
>= 84 days after infusion and no evidence of graft versus host disease
(GVHD)
- Autologous stem cell infusion including boost infusion: >= 42 days
- Cellular therapy: >= 42 days after the completion of any type of cellular therapy
(e.g. modified T cells, natural killer [NK] cells, dendritic cells, etc.)
- Radiation therapy (XRT)/external beam irradiation including protons: >= 14 days
after local XRT; >= 150 days after TBI, craniospinal XRT or if radiation to >=
50% of the pelvis; >= 42 days if other substantial bone marrow (BM) radiation;
Note: Radiation may not be delivered to "measurable disease" tumor site(s) being
used to follow response to subprotocol treatment
- Radiopharmaceutical therapy (e.g., radiolabeled antibody, 131I-MIBG): >= 42 days
after systemically administered radiopharmaceutical therapy
- Patients must not have had prior exposure to tazemetostat or other inhibitor(s)
of EZH2
- For patients with solid tumors without known bone marrow involvement:
- Peripheral absolute neutrophil count (ANC) >= 1000/mm^3
- Platelet count >= 100,000/mm^3 (transfusion independent, defined as not receiving
platelet transfusions for at least 7 days prior to enrollment)
- Hemoglobin >= 8.0 g/dL at baseline (may receive red blood cell [RBC]
transfusions)
- Patients with known bone marrow metastatic disease will be eligible for study provided
they meet the blood counts (may receive transfusions provided they are not known to be
refractory to red cell or platelet transfusions); these patients will not be evaluable
for hematologic toxicity
- Creatinine clearance or radioisotope glomerular filtration rate (GFR) >= 70
ml/min/1.73 m^2 or a serum creatinine based on age/gender as follows:
- Age 1 to < 2 years: male: 0.6 mg/dL; female: 0.6 mg/dL
- Age 2 to < 6 years: male: 0.8 mg/dL; female: 0.8 mg/dL
- Age 6 to < 10 years: male: 1 mg/dL; female: 1 mg/dL
- Age 10 to < 13 years: male: 1.2 mg/dL; female: 1.2 mg/dL
- Age 13 to < 16 years: male: 1.5 mg/dL; female: 1.4 mg/dL
- Age >= 16 years: male: 1.7 mg/dL; female: 1.4 mg/dL
- Bilirubin (sum of conjugated + unconjugated) =< 1.5 x upper limit of normal (ULN) for
age
- Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =< 135
U/L; (for the purpose of this study, the ULN for SGPT is 45 U/L)
- Serum albumin >= 2 g/dL
- Corrected QT (QTc) interval =< 480 milliseconds
- Patients with seizure disorder may be enrolled if on anticonvulsants and well
controlled
- Nervous system disorders (Common Terminology Criteria for Adverse Events [CTCAE]
version [V] 4.0) resulting from prior therapy must be =< grade 2, with the exception
of decreased tendon reflex (DTR). Any grade of DTR is eligible
- International normalized ratio (INR) =< 1.5
- For subjects with CNS involvement (primary tumor or metastatic disease): Subjects must
not have any active bleeding, or new intratumoral hemorrhage of more than punctate
size on screening MRI or known bleeding diathesis or treatment with anti-platelet or
anti-thrombotic agents
- All patients and/or their parents or legally authorized representatives must sign a
written informed consent; assent, when appropriate, will be obtained according to
institutional guidelines
Exclusion Criteria:
- Pregnant or breast-feeding women will not be entered on this study because there is
currently no available information regarding human fetal or teratogenic toxicities;
pregnancy tests must be obtained in girls who are post-menarchal; males or females of
reproductive potential may not participate unless they have agreed to use an effective
contraceptive method for the duration of study treatment; female subjects of
childbearing potential should agree to remain abstinent or use adequate contraceptive
methods for 30 days after the last dose of tazemetostat; male subjects should agree to
remain abstinent or use adequate contraceptive methods, and agree to refrain from
donating sperm, and for 90 days after the last dose of tazemetostat
- Patients receiving corticosteroids who have not been on a stable or decreasing dose of
corticosteroid for at least 7 days prior to enrollment are not eligible; if used to
modify immune adverse events related to prior therapy, >= 14 days must have elapsed
since last dose of corticosteroid
- Patients who are currently receiving another investigational drug are not eligible
- Patients who are currently receiving other anti-cancer agents are not eligible
- Patients who are receiving cyclosporine, tacrolimus or other agents to prevent
graft-versus-host disease post bone marrow transplant are not eligible for this trial
- Patients who are currently receiving drugs that are strong inducers or strong
inhibitors of CYP3A4 are not eligible; strong inducers or inhibitors of CYP3A4 are
prohibited from 14 days prior to the first dose of tazemetostat to the end of the
study; Note: Dexamethasone for CNS tumors or metastases, on a stable dose, is allowed
- Patients who have an uncontrolled infection are not eligible
- On complete blood count (CBC) differential, patients must not have any significant
morphologic abnormalities concerning for myeloproliferative neoplasm
(MPN)/myelodysplastic syndrome (MDS) or T- acute lymphoblastic leukemia (ALL)
- Patients must not have thrombocytopenia, neutropenia, or anemia of grade >= 3 (per
CTCAE 5.0 criteria) or any prior history of myeloid malignancies, including
myelodysplastic syndrome (MDS)
- Patients with a history of prior history of T-lymphoblastic lymphoma (LBL)/T-ALL
- Patients with any prior history of myeloid malignancies, including myelodysplastic
syndrome (MDS).
- Patients who have received prior solid organ transplantation are not eligible
- Patients who in the opinion of the investigator may not be able to comply with the
safety monitoring requirements of the study are not eligible