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Clinical Trials/NCT01041846
NCT01041846
Completed
Not Applicable

A Prospective Multicenter Observational Study for Dacogen Treatment in Patients With Myelodysplastic Syndrome

Janssen Korea, Ltd., Korea0 sites103 target enrollmentDecember 2008

Overview

Phase
Not Applicable
Intervention
No intervention
Conditions
Myelodysplastic Syndrome
Sponsor
Janssen Korea, Ltd., Korea
Enrollment
103
Primary Endpoint
Number of patients with complete remission
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effectiveness and safety of decitabine (Dacogen) intravenous injection in patients with Myelodysplastic Syndrome.

Detailed Description

This is a prospective (in which the patients are first identified and then followed forward as time passes), multi-center (study conducted at multiple sites), observational study (a scientific study to make a clear and easy understanding of the cause and effect relationship) to evaluate the effectiveness and safety information of a 5 day decitabine (Dacogen) regimen in patients with Myelodysplastic Syndrome. This study consist of 3 phases; pre-treatment phase, treatment phase and end of treatment (Day 28\~61 after last administration of Dacogen). The patients will receive decitabine intravenous injection 20 mg/m2 one hour once daily for 5 consecutive days for every 4 weeks. Safety evaluations including adverse events and clinical laboratory tests and will be evaluated with adverse events reported for the period ranging from informed consent and during the study to the end of treatment visit including 56 days (8 weeks) after the last administration of the clinical study treatment.

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
July 2010
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with (primary or secondary) Myelodysplastic Syndrome including chronic myelomonocytic leukemia (CMML) with an International Prognostic Scoring System more than or equal to Interferon-1
  • Patients who have never treated with hypomethylating agent (azacitidine and decitabine)
  • Female patients who are postmenopausal or received contraceptive operation or refrain from sexual relations.
  • Women of childbearing potential should conduct an effective method of birth control as defined in protocol, in case of male patients who will not have a baby within 2 months after the completion of decitabine therapy

Exclusion Criteria

  • Patients diagnosed with acute myelogenous leukemia (bone marrow stem cell counts exceeding 20 %) or other progressive malignant diseases
  • Patients with active infection of virus or bacteria
  • Patients who used to be treated with azacitidine or decitabine
  • Patients who are hypersensitive to excipients of decitabine
  • Patients who are pregnant and breast-feeding

Arms & Interventions

Decitabine

Intervention: No intervention

Outcomes

Primary Outcomes

Number of patients with complete remission

Time Frame: Up to 61 days

The complete response includes the evaluations of Bone marrow aspiration and biopsy (less than or equal to 5 percents myeloblast), persistent dysplasia and peripheral blood.

Number of patients with partial remission

Time Frame: Up to 61 days

The partial response includes all complete remission evaluating parameters with the exception of bone marrow blasts are decreased by more than or equal to 50 percents over pretreatment but still more than 5 percents and cellularity (the state of a tissue or other mass as regards the number of its constituent cells) and morphology (examination of structure)

Number of patients with hematological improvement

Time Frame: Up to 61 days

Response rate

Time Frame: After 4 cycles and end of treatment

Response rate is the combination of complete remission, partial remission and hematological improvement and performed according to the response criteria of 'International Working Group 2006' which is standardized criteria for assessing response are essential to ensure comparability among clinical trials for patients with MDS.

Secondary Outcomes

  • Cytogenetic response rate(Up to 61 days)
  • Overall survival rate(Up to 61 days)
  • Time to acute myeloid leukemia evolution(Up to 61 days)
  • Number of patients with progression-free survival status(Up to 61 days)
  • Number of patients with adverse event(Up to 61 days)

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