Study of Low-Dose Intravenous Decitabine in Patients Aged > 60 Years With Acute Myeloid Leukemia

Acute Myeloid Leukemia Clinical Trial

Official title:

Phase II Study of Low-Dose Intravenous Decitabine in Patients Aged > 60 Years With Acute Myeloid Leukemia Who Are Not Eligible for Standard Induction Chemotherapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00866073
• Other study ID #: 00331
• Status: Completed
• Phase: Phase 2
• First received: March 19, 2009
• Last updated: March 19, 2009
• Start date: April 2003
• Est. completion date: March 2009

Study information

• Verified date: March 2009
• Source: University Hospital Freiburg
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

This study is an open-label phase II trial to investigate the efficacy and toxicity of low-dose decitabine (5-aza-2'-deoxycytidine) in elderly patients with acute myeloid leukemia (AML) not eligible for aggressive induction chemotherapy. AML patients above the age of 60 years (no upper age limit) who have not previously received and are not eligible for, standard induction treatment of their disease will be eligible for this trial. Decitabine will be administered as a 3 hour infusion at 15 mg/m2 three times daily on three consecutive days (total dose 135 mg/m2). In all patients with > 20000 WBC/µl, this treatment will be repeated 1 week later. In patients with white blood cells exceeding 50 000/μl, decitabine treatment will be preceded by cytoreductive doses of hydroxyurea.

Description:

Hypothesis: If after 4 courses of Decitabine none out of 12 patients achieves a response (complete or partial remission, antileukemic effect), the protocol will be stopped. If at least one response is seen among the first 12 patients, 17 additional patients will be treated in an open, uncontrolled manner. If in 3 or more of these 29 patients a response is achieved, this treatment will be considered effective and will be studied further, otherwise it will be considered ineffective. At a preliminary analysis after recruitment of 29 patients, encouraging results (response rate, tolerability) are prompting continuation of recruitment, with a planned inclusion of at least 60 patients, until initiation of the planned large, controlled phase II follow-up trial. Unexpected toxicities will be carefully evaluated. 29 patients were needed for the first two steps of this phase II study, at least 60 patients are planned for the extension of the recruitment. Expected study duration for the first two steps was 15-20 months, with 35-40 months total when including the third step.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 238
• Est. completion date: March 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• Patients older than 60 years with acute myeloid leukemia (> 30 % bone marrow blasts) not qualifying for, or not consenting to, standard induction chemotherapy or immediate allografting

• life expectancy > 3 months with successful treatment

• performance status ECOG 0, 1, 2

• age-adjusted normal cardiac, kidney, liver function (creatinine < 1.5 mg/dl unless leukemia-related, total bilirubin < 2.0 of upper normal limits)

• patients with >50 000 leukocytes/µl in whom initial cytoreduction according to protocol is effective

• written informed consent

Exclusion Criteria:

• AML of FAB subtype M3

• previous induction-type chemotherapy for MDS or AML

• previous treatment with Decitabine, 5-azacytidine or ATRA

• "low-dose" chemotherapy (e.g.hydroxyurea, cytosine arabinoside, melphalan) within 8 weeks prior to Decitabine treatment, except for cytoreduction of leukocytosis > 50 000/µl according to protocol - patients with > 50 000 leukocytes/µl in whom initial cytoreduction according to protocol is ineffective

• treatment with cytokines within previous 4 weeks

• concomitant use of any other investigational drug

• other malignancy that is not in remission (previous chemotherapy for other malignancies is not an exclusion criteria)

• cardiac insufficiency NYHA IV

• HIV infection

• other uncontrolled active infection

• psychiatric disorder that interferes with treatment

• known hypersensitivity to retinoids

• contact lenses

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Decitabine 15 mg/m2 i.v.
Decitabine at 15 mg/m2 i.v. x 3 hours, three times daily on three consecutive days

Locations

Country	Name	City	State
Germany	Klinikum der Technischen Universität Aachen	Aachen
Germany	Universitätsklinikum Düsseldorf	Düsseldorf
Germany	Katholisches Krankenhaus Hagen	Hagen
Germany	Medizinische Hochschule Hannover	Hannover	Niedersachsen
Germany	Klinikum Lüdenscheid	Luedenscheid
Germany	Universitätsklinikum Ulm	Ulm
Germany	Klinikum Villingen-Schwenningen	Villingen-Schwenningen
Netherlands	Leyenburg Hospital	The Hague

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital Freiburg

Countries where clinical trial is conducted

Germany,  Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	response rate (complete and partial remissions, antileukemic effect)		after four treatment courses of Decitabine, after 6 months	No
Secondary	overall survival		after 1 year	No
Secondary	progression-free survival time		after 1 year	No
Secondary	toxicity of Decitabine (alone and in combination with all-trans retinoic acid)		after 3-6 months	Yes