|Phase I||Biomarker/Laboratory analysis, Treatment||Active||21 and over||NCI||NCI-2011-01436|
J09112, CDR0000671796, JHOC-MD017, U01CA070095, SKCCC-MD017, 8298, NCT01132573
This phase I trial is studying the side effects and best dose of entinostat when given together with clofarabine in treating patients with newly diagnosed, relapsed, or refractory poor-risk acute lymphoblastic leukemia or bilineage/biphenotypic leukemia. Entinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as clofarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving entinostat together with clofarabine may kill more cancer cells.
Further Study Information
I. To determine the feasibility, tolerability, toxicities, and maximum tolerated dose (MTD) of entinostat plus clofarabine for: adult patients age 40 and over with newly diagnosed, poor-risk Philadelphia chromosome negative (Ph-) acute lymphoblastic leukemia (ALL) or bilineage/biphenotypic leukemia (ABL) prior to traditional cyclical multi-agent chemotherapy, and adults age 21 and over with relapsed or refractory ALL/ABL.
II. To determine if entinostat plus clofarabine can induce clinical responses in adults with newly diagnosed, poor-risk ALL/ABL and in adults with relapsed/refractory ALL/ABL
I. To determine pharmacokinetics (PK) of entinostat alone and in combination with clofarabine.
II. To obtain descriptive preliminary pharmacodynamic (PD) data regarding the effects of entinostat alone and in combination with clofarabine on histone acetylation and global and gene specific methylation in leukemic blasts.
III. To obtain descriptive preliminary data regarding the effects of entinostat alone and in combination with clofarabine on DNA damage and apoptosis in leukemic blasts and residual disease monitored by 6-color flow cytometry.
OUTLINE: This is a multicenter, dose-escalation study of entinostat.
Patients receive entinostat orally (PO) on days 1 and 8 and clofarabine intravenously (IV) over 2 hours on days 3-7. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity (only for patients at least 60 years of age with newly diagnosed acute lymphoblastic leukemia [ALL] or bilineage/biphenotypic leukemia [ABL] who are unable or unwilling to tolerate standard multi-agent chemotherapy and patients with relapsed or refractory ALL or ABL).
Patients 40-59 years of age with newly diagnosed ALL receive standard multi-agent induction chemotherapy beginning on day 11. Patients at least 21 years of age in their first relapse with sensitive disease begin initiation of allogeneic transplant after one course of entinostat and clofarabine.
Blood and/or bone marrow samples are collected periodically for pharmacological and laboratory analysis.
After completion of study treatment, patients are followed up for 30 days.
- Meets one of the following criteria:
- Adults age >= 40 years with the established, pathologically-confirmed diagnoses of newly diagnosed acute lymphoblastic leukemia (ALL) or bilineage/biphenotypic leukemia (ABL)
- Adults with relapsed and refractory ALL or ABL who are >= 21 years of age and who have progressive disease following their last therapy
- For adults with relapsed/refractory ALL, no more than 5 previous regimens
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Patients must be able to give informed consent
- Female patients of childbearing age must have negative pregnancy test
- Total white blood cell count (WBC) =< 150,000 with no evidence for ongoing or impending leukostasis
- Total bilirubin =< 2.0 mg/dL unless elevated due to Gilbert's disease, hemolysis or leukemic infiltration
- Aspartate transaminase (AST)/alanine transaminase (ALT) =< 2.5 × upper limit of normal (ULN) unless due to leukemic infiltration
- Serum creatinine =< 2.0 mg/dL
- Left ventricular ejection fraction (LVEF) >= 45% as measured by echocardiogram (ECHO) or multiple gated acquisition (MUGA) scan
- Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for 30 days after study participation
- Patients who have undergone stem cell transplantation (SCT), autologous or allogeneic, are eligible provided that they are >= 4 weeks from stem cell infusion, have no active graft-vs-host disease (GVHD), and meet other eligibility criteria
- Patients who fail primary induction therapy or relapse after achieving complete remission (CR) are eligible if they have undergone no more than 5 prior cytotoxic regimen, >= 14 days off cytotoxic chemotherapy, and >= 2 weeks radiation therapy; patients must be off biologic therapies >= 7 days, must be off hematopoietic growth factors >= 3 days; if using hydroxyurea steroids, imatinib, arsenic, interferon, or other non-cytotoxics for blast count control, patient must be off for >= 24 hrs before starting entinostat plus clofarabine
- Philadelphia chromosome positive ALL
- Patients may not have received previous treatment with entinostat or other histone deacetylase (HDAC) inhibitors (including valproic acid) or clofarabine within the previous 6 months
- Concomitant chemotherapy, radiation therapy, or immunotherapy
- Hyperleukocytosis with >= 150,000 blasts/uL (If using hydroxyurea, steroids, maintenance doses of 6-mercaptopurine and/or methotrexate, arsenic, interferon or leukopheresis for blast count control, patient must be off those agents for 24 hours prior to beginning entinostat plus clofarabine)
- Active disseminated intravascular coagulation
- Active central nervous system (CNS) leukemia; patients with known previous CNS leukemia may continue to receive intrathecal therapy with cytarabine (ara-C), methotrexate, and/or thiotepa plus steroids as prophylaxis against reactivation of active CNS disease
- Use of investigational cytotoxic agents within 30 days or any anticancer therapy within 14 days before study entry, except for hydroxyurea and steroids, both of which must be discontinued at least 24 hours before study entry
- The patient must have recovered from all acute toxicities from any previous therapy
- Patients must have discontinued all growth factors at least 3 days before study
- History of severe coronary artery disease, including myocardial infarction within the previous 3 months, arrhythmias other than atrial flutter or fibrillation requiring medication, or uncontrolled congestive heart failure
- Dyspnea at rest or with minimal exertion
- Active uncontrolled infection (patients with infection under active treatment and controlled with antibiotics are eligible)
- Patients with active >= grade 2 GVHD
- Presence of other life-threatening illness
- Patients with mental deficits and/or psychiatric history that preclude them from giving informed consent or from following protocol
- Pregnant or nursing
- Male and female patients who are fertile who do not agree to use an effective barrier method of birth control (ie, hormonal or barrier method of birth control; abstinence) to avoid pregnancy during the study and for a minimum of 30 days after study treatment
- Previous history of or current seizure disorder
- Human immunodeficiency virus (HIV) infected patients who have CD4 cell count =< 350/mm^3 or a history of acquired immunodeficiency syndrome (AIDS)-defining conditions
Trial Lead Organizations/Sponsors
National Cancer Institute
|Hetty Carraway||Principal Investigator|
|University of Colorado Cancer Center at UC Health Sciences Center|
|Lia Gore||Ph: 303-724-4011|
|Lia Gore||Principal Investigator|
|Greenebaum Cancer Center at University of Maryland Medical Center|
|Ivana Gojo||Ph: 410-328-2596|
|Ivana Gojo||Principal Investigator|
|Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins|
|Hetty E. Carraway||Ph: 410-502-3809|
|Hetty E. Carraway||Principal Investigator|
Link to the current ClinicalTrials.gov record.
NLM Identifer NCT01132573
Information obtained from ClinicalTrials.gov on April 16, 2013
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