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Clinical Trials/NCT01350947
NCT01350947
Completed
Phase 2

A Phase II Study of the Efficacy, Safety and Determinants of Response to 5-Azacitidine (Vidaza®) in Patients With Chronic Myelomonocytic Leukemia (CMML)

University of Utah3 sites in 1 country11 target enrollmentApril 2011

Overview

Phase
Phase 2
Intervention
5-Azacitidine
Conditions
Chronic Myelomonocytic Leukemia
Sponsor
University of Utah
Enrollment
11
Locations
3
Primary Endpoint
Percentage of Patients With Complete Hematologic Response (According to IWG 2006 Criteria) in CMML Patients Treated With 5-azacitidine.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The primary objective of this study is:

Response to treatment will be evaluated according to the revised International Working Group (IWG) categories natural history, hematologic improvement and cytogenetic response1;2. The primary objective is:

To determine the rate of complete hematologic response and hematologic improvement (according to IWG 2006 criteria) in CMML patients treated with 5-azacitidine.

Detailed Description

In this study, eligible patients with a confirmed diagnosis of CMML will be treated with 5-azacitidine to determine the rates of complete hematologic response, hematologic improvement, complete and partial cytogenetic response, and overall and progression free survival. To develop biomarkers associated with response and gain insights into the mechanisms that determine response, gene expression profiling, genome-wide SNP array analysis, microRNA analysis, and DNA methylation analysis will be performed prior to therapy and at defined time points during the study. Phosphoproteomics profiling may be included in the analysis.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
September 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of CMML as defined by the WHO criteria
  • Persistent peripheral blood monocytosis of more than 1 x 109/L for at least 3 months and
  • No Philadelphia chromosome or BCR-ABL fusion gene and
  • Less than 20% blasts in the blood or bone marrow and
  • Dysplasia in one or more of the myeloid lineages\* \* In the absence of dysplasia in one or more of the myeloid lineages, the diagnosis of CMML can still be made if a) - c) are met AND an acquired clonal chromosomal abnormality is present in the bone marrow cells, the monocytosis has been present for more than 3months AND all other causes of monocytosis have been ruled out.
  • Age of 18 years or older. Both men and women and members of all races and ethnic groups will be included.
  • ECOG performance status \<3
  • Adequate organ function defined as:
  • Total bilirubin \<2.5 x upper limit of normal (ULN)
  • Direct bilirubin \<2 x ULN

Exclusion Criteria

  • Progression to acute myeloid leukemia (defined by at least 20% blasts in the blood or bone marrow). In the unlikely event that progression to acute leukemia is demonstrated in the "screening" bone marrow biopsy, it is at the discretion of the investigator to enroll the patient after adequate discussion of the findings and alternative therapies. Enrollment of such a patient must be reported to the HCI PI.
  • Presence of activating mutations of the platelet derived growth factor receptors alpha or beta, which would suggest likely benefit from imatinib treatment (these mutations will usually be obvious from karyotyping and fluorescence in situ hybridization studies)
  • Known or suspected hypersensitivity to 5-azacitidine or mannitol
  • Clinically significant heart disease (New York Heart Association Class III or IV) or other serious intercurrent illnesses or psychiatric illness/social situations that would limit compliance with study requirements
  • Major surgery within 28 days before registration (exception: central venous line placement), or lack of full recovery from prior major surgery
  • Prior therapy with a hypomethylating agent
  • Cytotoxic chemotherapy less than 2 weeks prior to starting study medication (exception: hydroxyurea and/or anagrelide)
  • Erythropoietin or darbepoietin, G-CSF, GM-CSF, thalidomide or lenalidomide less than 2 weeks from day 1 of cycle 1
  • Concomitant cytotoxic chemotherapy (exception: hydroxyurea for up to 1 week per cycle)
  • Concomitant therapy with other investigational agents

Arms & Interventions

All patients

All participants enrolled.

Intervention: 5-Azacitidine

Outcomes

Primary Outcomes

Percentage of Patients With Complete Hematologic Response (According to IWG 2006 Criteria) in CMML Patients Treated With 5-azacitidine.

Time Frame: 24 months

Complete Hematologic Response is defined as: bone marrow evaluation shows \<= 5% myeloblasts with normal maturation of all cells lines; peripheral blood evaluation shows hemoglobin \>= 11 g/dL, neutrophils \>= 1000/mL, platelets \>= 100,000/mL, 0% blasts

Study Sites (3)

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