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Safety of Zileuton (Zyflo) in Combination With Imatinib Mesylate (Gleevec) in CML.

Primary Purpose

Chronic Myelogenous Leukemia

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Zileuton
Sponsored by
University of Massachusetts, Worcester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Myelogenous Leukemia focused on measuring Leukemia, Zileuton, myeloproliferative neoplasm

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with CML in chronic phase (patients already on imatinib)
  • Presence of Philadelphia chromosome or bcr-abl rearrangement
  • Age ≥ 18 years
  • ECOG performance status ≤ 2
  • Written informed consent

Exclusion Criteria:

  • Hepatic dysfunction (serum bilirubin ≥ 2 x ULN, and/or ALT ≥ 3 x ULN, and/or AST ≥ 3 x ULN)
  • Renal dysfunction (creatinine ≥ 200 μmol/l or 2.3 mg/dl)
  • Severe cardiac dysfunction (NYHA classification III-IV)
  • Severe pulmonary or neurologic disease
  • Pregnant or lactating females
  • Patients with a history of active malignancy during the past 5 years with the exception of nonmetastatic skin cancer (e.g. treated squamous or basal cell carcinoma) or stage 0 cervical carcinoma
  • Patients known to be HIV-positive
  • Patients with active, uncontrolled infections
  • Male and female patients of reproductive potential who are not practicing effective means of contraception
  • Patients with known allergic reaction or intolerance to either imatinib or zileuton
  • Patients requiring anticoagulation therapy with coumadin

Sites / Locations

  • University of Massachusetts Medical School

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

single arm of experimental drug combination

Arm Description

Outcomes

Primary Outcome Measures

To define toxicity and safety profile of zileuton combined with imatinib in patients with CML

Secondary Outcome Measures

To assess the efficacy of zileuton combined with imatinib in terms of (See Description)
Level of 5-lipoxygenase (5-LO) blockade The rate of complete hematological response The rate of complete cytogenetic response The rate of major molecular response

Full Information

First Posted
May 24, 2010
Last Updated
May 26, 2015
Sponsor
University of Massachusetts, Worcester
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1. Study Identification

Unique Protocol Identification Number
NCT01130688
Brief Title
Safety of Zileuton (Zyflo) in Combination With Imatinib Mesylate (Gleevec) in CML.
Official Title
Phase I Study to Evaluate the Safety of Zileuton (Zyflo) in Combination With Imatinib Mesylate (Gleevec) in Patients With Chronic Myelogenous Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Terminated
Why Stopped
Lack of enrollment
Study Start Date
January 2010 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Massachusetts, Worcester

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The leukemic stem cells (LSCs) are cells that self- renew and give rise to leukemia. Eradication of LSC is required for cure. In chronic myelogenous leukemia (CML) LSCs are not eradicated by imatinib (Gleevec) alone. Recent discovery by Dr. Shaoguang Li at University of Massachusetts indicates that the LSCs can be targeted by a new drug zileuton (Chen et al. Nature Genetics 2009; 41:783-792). Zileuton (approved for asthma) will be tested in a combination with Gleevec. This combination has not been used previously to treat leukemia. This is a Phase I study. The goal of this research is to evaluate the safety of the standard anti-cancer drug imatinib and experimental drug zileuton.
Detailed Description
More than twenty two thousand people live with chronic myelogenous leukemia in the United States and more than five thousand people are expected to be diagnosed this year. The majority of patients with this disease are diagnosed in what is called the chronic phase. The standard treatment for this phase of the disease is therapy with a medication called imatinib. This treatment can diminish the amount of disease to very low levels that only very sensitive and specialized techniques can measure; it does not, however, provide a cure. Dr. Shaoguang Li and colleagues at University of Massachusetts have published a unique discovery that the arachidonate 5-lipoxygenase (5-LO) gene (Alox5) is a critical regulator for LSCs in BCR-ABL-induced CML (Chen Y et al. Loss of the Alox5 gene impairs leukemia stem cells and prevents chronic myeloid leukemia. Nature Genetics 41:783-792, 2009). In the absence of Alox5, BCR-ABL failed to induce CML in preclinical studies. While deficiency in Alox5 had no effect on normal hematopoiesis, impairment of the LSCs function through differentiation and cell division of CML LSCs was observed. This defect led to a depletion of LSCs and a failure of CML development. Treatment with a 5-LO inhibitor (zileuton) also impaired the function of LSCs and prolonged survival. These results demonstrate that a specific target gene can be found in cancer stem cells and its inhibition can completely inhibit the function of these stem cells. These findings provide an exciting opportunity to develop the first anti-cancer stem cell therapy for treating CML.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Myelogenous Leukemia
Keywords
Leukemia, Zileuton, myeloproliferative neoplasm

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
single arm of experimental drug combination
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Zileuton
Other Intervention Name(s)
Zyflo
Intervention Description
Imatinib combined with Zileuton
Primary Outcome Measure Information:
Title
To define toxicity and safety profile of zileuton combined with imatinib in patients with CML
Time Frame
Throughout the study
Secondary Outcome Measure Information:
Title
To assess the efficacy of zileuton combined with imatinib in terms of (See Description)
Description
Level of 5-lipoxygenase (5-LO) blockade The rate of complete hematological response The rate of complete cytogenetic response The rate of major molecular response
Time Frame
Throughout the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with CML in chronic phase (patients already on imatinib) Presence of Philadelphia chromosome or bcr-abl rearrangement Age ≥ 18 years ECOG performance status ≤ 2 Written informed consent Exclusion Criteria: Hepatic dysfunction (serum bilirubin ≥ 2 x ULN, and/or ALT ≥ 3 x ULN, and/or AST ≥ 3 x ULN) Renal dysfunction (creatinine ≥ 200 μmol/l or 2.3 mg/dl) Severe cardiac dysfunction (NYHA classification III-IV) Severe pulmonary or neurologic disease Pregnant or lactating females Patients with a history of active malignancy during the past 5 years with the exception of nonmetastatic skin cancer (e.g. treated squamous or basal cell carcinoma) or stage 0 cervical carcinoma Patients known to be HIV-positive Patients with active, uncontrolled infections Male and female patients of reproductive potential who are not practicing effective means of contraception Patients with known allergic reaction or intolerance to either imatinib or zileuton Patients requiring anticoagulation therapy with coumadin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jan Cerny, MD, PhD
Organizational Affiliation
University of Massachusetts, Worcester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Medical School
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19503090
Citation
Chen Y, Hu Y, Zhang H, Peng C, Li S. Loss of the Alox5 gene impairs leukemia stem cells and prevents chronic myeloid leukemia. Nat Genet. 2009 Jul;41(7):783-92. doi: 10.1038/ng.389. Epub 2009 Jun 7.
Results Reference
result
PubMed Identifier
17151364
Citation
Druker BJ, Guilhot F, O'Brien SG, Gathmann I, Kantarjian H, Gattermann N, Deininger MW, Silver RT, Goldman JM, Stone RM, Cervantes F, Hochhaus A, Powell BL, Gabrilove JL, Rousselot P, Reiffers J, Cornelissen JJ, Hughes T, Agis H, Fischer T, Verhoef G, Shepherd J, Saglio G, Gratwohl A, Nielsen JL, Radich JP, Simonsson B, Taylor K, Baccarani M, So C, Letvak L, Larson RA; IRIS Investigators. Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. N Engl J Med. 2006 Dec 7;355(23):2408-17. doi: 10.1056/NEJMoa062867.
Results Reference
result

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Safety of Zileuton (Zyflo) in Combination With Imatinib Mesylate (Gleevec) in CML.

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