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Phase I/II Clinical Study of SU11248 (Sutent) Combined With Standard Chemotherapy With Cytosine Arabinoside and Daunorubicin in Patients With FLT3 Mutated AML Over 60 Years of Age

Phase 1/Phase 2
60 Years
Open (Enrolling)
Acute Myeloid Leukemia

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Trial Information

Phase I/II Clinical Study of SU11248 (Sutent) Combined With Standard Chemotherapy With Cytosine Arabinoside and Daunorubicin in Patients With FLT3 Mutated AML Over 60 Years of Age

Inclusion Criteria:

- Patients with primary or secondary acute myeloid leukemia (any FAB type, except M3).

- No prior systemic chemotherapy for AML except hydroxyurea. Cytoreductive therapy with
hydroxyurea is recommended if WBC is > 50.000/µl, but should cease at least one day
prior to starting study medication

- Patient age equal or of greater than 60 years

- Patients must have FLT3 mutated AML, either ITD or kinase domain mutations

- ECOG Performance score 3 or less (Karnofsky Performance Score >40%).

- Life expectancy more than four weeks.

- Adequate hepatic and renal function, as defined by serum transaminases <2.5x ULN,
bilirubin <1.5x ULN. Creatinine <1.5x ULN.

- Patients must provide written informed consent to participate in the trial.

- Normal heart function on cardiac ultrasound

- Prothrombin time (PT) and partial thromboplastin time (PTT) <=1.5 x ULN

- Serum albumin >=3.0 g/dl

- Serum amylase and lipase <=1.0 x ULN

- Willingness and ability to comply with scheduled visits, treatment plans, laboratory
tests, and other study procedures.

Exclusion Criteria:

The presence of any of the following will exclude a subject from study enrollment:

- Treatment with any investigational agent within four weeks.

- Known HIV infection

- Presence of any medical or psychiatric condition which may limit full compliance with
the study, including but not limited to:

- Presence of CNS leukaemia

- Unresolved toxicity from previous anti-cancer therapy or incomplete recovery from

- Any of the following within the 12 months prior to study drug administration:
myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass
graft, symptomatic congestive heart failure, cerebrovascular accident or transient
ischemic attack, pulmonary embolism, deep vein thrombosis, or other thromboembolic

- Current treatment with therapeutic doses of anticoagulant (low dose Coumadin up to 2
mg PO daily for deep vein thrombosis prophylaxis is allowed).

- Hypertension that cannot be controlled by medications (>150/100 mmHg despite optimal
medical therapy).

- Pre existing thyroid abnormality of thyroid function that cannot be maintained in the
normal range with medication.

- Ongoing cardiac dysrhythmias of NCI CTCAE Grade >=2, atrial fibrillation of any
Grade, or prolongation of the QTc interval to >450 msec for males or >470 msec for

- Other severe acute or chronic medical or psychiatric condition, or laboratory
abnormality that may increase the risk associated with study participation or study
drug administration, or may interfere with the interpretation of study results, and
in the judgment of the investigator would make the patient inappropriate for entry
into this study.

Type of Study:


Study Design:

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

Outcome Measure:

Definition of a recommended Phase III dose and determination CTC version 3.0 grade 3-5 non-hematological toxicities of SU11248 in combination with standard induction and consolidation chemotherapy

Outcome Time Frame:

April 2011

Safety Issue:


Principal Investigator

Walter Fiedler

Investigator Role:

Principal Investigator

Investigator Affiliation:

Universitätsklinikum Hamburg-Eppendorf


Germany: Federal Institute for Drugs and Medical Devices

Study ID:

AMLSG 10/07



Start Date:

August 2008

Completion Date:

Related Keywords:

  • Acute Myeloid Leukemia
  • AML
  • FLT3
  • acute myeloid leukemia
  • FLT 3 inhibitor
  • FLT3 mutated AML
  • Leukemia
  • Leukemia, Myeloid, Acute
  • Leukemia, Myeloid