Sunitinib in Treating Patients With Myelodysplastic Syndromes or Chronic Myelomonocytic Leukemia

NCT ID: NCT00451048

Last Updated: 2018-09-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-02-28
• Study Completion Date: 2012-10-31

Brief Summary

This phase II trial is studying how well sunitinib works in treating patients with myelodysplastic syndromes or chronic myelomonocytic leukemia. Sunitinib may stop the growth of abnormal cells by blocking some of the enzymes needed for cell growth.

Detailed Description

OBJECTIVES:

I. Determine the overall response rate (complete response, partial response, or hematological improvement) in patients with intermediate-2 or high-risk myelodysplastic syndromes or chronic myelomonocytic leukemia treated with sunitinib malate.

II. Determine the duration of response in patients treated with this drug. III. Determine the overall survival of patients treated with this drug. IV. Determine the progression-free survival of patients treated with this drug. V. Determine the time to disease progression in patients treated with this drug.

VI. Determine the toxicity of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive oral sunitinib malate once daily on days 1-28. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed at 3-4 weeks and then monthly thereafter.

Conditions

Chronic Myelomonocytic Leukemia; de Novo Myelodysplastic Syndromes; Myelodysplastic Syndromes; Secondary Myelodysplastic Syndromes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients will receive sunitinib malate (SU11248) by mouth once a day. Treatment may continue for as long as benefit is shown.

Group Type: EXPERIMENTAL

sunitinib malate

Intervention Type: DRUG

Given orally

Interventions

sunitinib malate

Given orally

Intervention Type: DRUG

Other Intervention Names

SU11248; sunitinib; Sutent

Eligibility Criteria

Inclusion Criteria

• MDS syndromes meeting 1 of the following: Intermediate-2 disease, high-risk disease (IPSS score>=1.5)
• CMML: WBC>12,000/mm^3, Intermediate-2 disease with WBC=<12,000/mm^3, high-risk disease (IPSS score>=1.5) with WBC=<12,000/mm^3
• Patients with insufficient/inadequate metaphases for cytogenetic analysis are eligible if bone marrow blasts are >10% and/or 2-3 cytopenias are present
• No known brain metastases
• Life expectancy>12 weeks
• ECOG PS 0-2/Karnofsky PS 60-100%
• Calcium=<3.0 mmol/L
• Bilirubin normal
• AST and ALT=<2.5 times upper limit of normal
• Creatinine normal/creatinine clearance>=60 mL/min

Exclusion Criteria

• No history of significant ECG abnormalities including but not limited to: ventricular arrhythmias (ventricular tachycardia, ventricular fibrillation>=3 beats in a row); QTc prolongation (i.e.QTc interval>=500msec)
• No history of allergic reaction to compounds of similar chemical/biological composition to sunitinib malate
• No NYHA class III-IV congestive heart failure
• Patients with history of NYHA class II congestive heart failure who are asymptomatic on treatment are eligible
• No abdominal fistula/G perforation/intraabdominal abscess within past 28 days
• No serious cardiovascular disease within past 12 months including: cerebrovascular accident or transient ischemic attack, myocardial infarction, cardiac arrhythmia, stable or unstable angina, symptomatic congestive heart failure, coronary or peripheral artery bypass graft or stenting
• No pulmonary embolism within past 12 months
• No uncontrolled hypertension (systolic BP>=140 mmHg/diastolic BP>=90 mmHg)
• No condition impairing ability to swallow/retain sunitinib malate tablets including: GI tract disease resulting in inability to take oral medication, requirement for IV alimentation, prior surgical procedures affecting absorption, active peptic ulcer disease
• No serious/nonhealing wound, ulcer, or bone fracture
• No uncontrolled pre-existing thyroid abnormality
• No concurrent uncontrolled illness including ongoing/active infection
• No psychiatric illness/social situation that would preclude study participation
• Not pregnant/nursing
• Negative pregnancy test
• Fertile patients must use effective barrier contraception
• 4 weeks since prior major surgery
• Prior central thoracic radiotherapy that included heart in radiotherapy port allowed provided NYHA congestive heart failure=<class II
• Prior anthracycline exposure allowed provided NYHA congestive heart failure=<class II
• No other prior therapy for MDS/CMML except epoetin alfa, darbepoetin alfa, filgrastim or sargramostim
• At least 2 weeks since prior epoetin alfa
• At least 4 weeks since prior darbepoetin alfa
• No other prior antiangiogenic agents including but not limited to: bevacizumab, sorafenib tosylate, pazopanib hydrochloride, AZD2171, vatalanib, VEGF Trap
• More than 7 days since prior and no concurrent potent CYP3A4 inhibitors
• More than 12 days since prior and no concurrent potent CYP3A4 inducers including: Rifampin, Rifabutin, Carbamazepine, Phenobarbital, Phenytoin, Hypericum perforatum, Efavirenz, Tipranavir
• No concurrent birth control patch/oral birth control pills/depot/injectable birth control methods
• No concurrent therapeutic coumarin-derivative anticoagulants
• Low dose(=<2mg) warfarin for prophylaxis of thrombosis allowed
• Low molecular weight heparin allowed if INR=<1.5
• No concurrent agents with proarrhythmic potential including: Terfenadine, Quinidine, Procainamide, Disopyramide, Sotalol, Probucol, Bepridil, Haloperidol, Risperidone, Indapamide, Flecainide acetate
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No other concurrent investigational agents

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Karen Yee

Role: PRINCIPAL_INVESTIGATOR

University Health Network-Princess Margaret Hospital

Locations

Roswell Park Cancer Institute

Buffalo, New York, United States

London Regional Cancer Program

London, Ontario, Canada

Odette Cancer Centre- Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

University Health Network-Princess Margaret Hospital

Toronto, Ontario, Canada

Countries

United States; Canada

Other Identifiers

PHL-063

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

CDR0000535656

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

N01CM62203

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2009-00211

Identifier Type: -

Identifier Source: org_study_id