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| ID | Type | Description | Link |
|---|---|---|---|
| MC058F | |||
| CDR0000560703 | Registry Identifier | PDQ (Physician Data Query) | |
| N01CM62205 | U.S. NIH Grant/Contract | View source |
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This phase II trial is studying how well sunitinib works in treating patients with relapsed multiple myeloma. Sunitinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the cancer
PRIMARY OBJECTIVES:
I. To assess the number of responses in patients with relapsed multiple myeloma treated with sunitinib (sunitinib malate).
SECONDARY OBJECTIVES:
I. To assess the toxicity of sunitinib malate in patients with relapsed multiple myeloma.
II. To assess time to progression after initial response to sunitinib malate.
OUTLINE:
Patients receive oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed every 3-6 months for up to 3 years.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment (kinase inhibitor therapy) | Experimental | Patients receive 37.5 mg oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| sunitinib malate | Drug | Oral 37.5 mg each day of the 6-week cycle (continuous dosing). |
|
| Measure | Description | Time Frame |
|---|---|---|
| The Number of Confirmed Responses (Complete Response [CR], Very Good Partial Response [VGPR], or Partial Response [PR]) | A confirmed response is defined as a patient who has achieved response and maintained it on two consecutive evaluations at least 2 weeks apart. A Complete Response (CR) is defined as the complete disappearance of an M-protein and fewer than 5% bone marrow plasmacytosis. A Hematologic Very good partial response (VGPR) is defined as having a ≥ 90% reduction of M-protein from serum, a Urine M-spike to be ≤ 100 mg/24 hours, and a disappearance of soft tissue plasmacytomas. A Partial Response (PR) is defined as having a 50-89% reduction in the level of the serum monoclonal protein, a reduction in 24-hour urinary light chain excretion either by ≥90% or to <200 mg, and a ≥ 50% reduction in size of soft tissue plasmacytoma. | Every 6 weeks from the first initiation of therapy up to 72 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Event-free Survival | The distribution of progression-free survival will be estimated using the method of Kaplan-Meier. | Time from registration to progression or death due to any cause, assessed up to 3 years |
| Duration of Response |
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Inclusion Criteria:
Diagnosis of relapsed multiple myeloma
Measurable disease as defined by at least one of the following:
Not a candidate for stem cell transplantation OR have undergone prior stem cell collection
Eastern Cooperative Oncology Group (ECOG) performance status 0-2
Life expectancy ≥ 3 months
Absolute neutrophil count ≥ 1,000/microliter (mcL)
Platelets ≥ 75,000/mcL
Hemoglobin ≥ 8 g/dL
Total serum bilirubin normal
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x upper limit of normal
Creatinine < 2.5 mg/dL
Negative pregnancy test for women of childbearing potential
No more than 4 prior therapies
Prior anthracycline exposure or central thoracic radiotherapy that included the heart in the radiotherapy port allowed provided patient has a New York Heart Association (NYHA) class II or better cardiac function on baseline ECHO or multiple gated acquisition scan (MUGA)
Concurrent bisphosphonates allowed
At least 7 days since prior and no concurrent cytochrome P450 3A4 (CYP3A4) inhibitors
At least 12 days since prior and no concurrent CYP3A4 inducers
Exclusion Criteria:
Pregnant or nursing women
History of allergic reactions attributed to compounds of similar chemical or biologic composition to sunitinib malate
History of serious ventricular arrhythmia or corrected QT interval (QTc) prolongation
Poorly controlled hypertension
Any condition that impairs the ability to swallow and retain sunitinib malate tablets
Patients with a preexisting thyroid abnormality who are unable to maintain thyroid function in the normal range with medication
Other active malignancy except nonmelanoma skin cancer or carcinoma in situ of the cervix or breast
Concurrent uncontrolled illness including, but not limited to, ongoing or active infections or psychiatric illness/social situations that would limit compliance with study requirements
Patients who have not recovered from adverse events of prior therapy
Chemotherapy or radiotherapy ≤ 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to study entry
Any major surgery ≤ 4 weeks prior to study entry
Nonmyelosuppressive agents ≤ 2 weeks prior to study entry
Any other prior antiangiogenic agents
Concurrent high-dose corticosteroids
Concurrent therapeutic doses of coumarin-derivative anticoagulants
Concurrent agents with proarrhythmic potential
Concurrent combination antiretroviral therapy for HIV-positive patients
Any other concurrent investigational agents or anticancer therapy
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| Name | Affiliation | Role |
|---|---|---|
| Shaji Kumar | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic Cancer Research Consortium | Rochester | Minnesota | 55905 | United States |
All 13 participants were analyzed.
Thirteen participants were accrued from September 2007 to December 2008.
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| ID | Title | Description |
|---|---|---|
| FG000 | Treatment (Kinase Inhibitor Therapy) | Patients receive oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Treatment (Kinase Inhibitor Therapy) | Patients receive oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Median |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | The Number of Confirmed Responses (Complete Response [CR], Very Good Partial Response [VGPR], or Partial Response [PR]) | A confirmed response is defined as a patient who has achieved response and maintained it on two consecutive evaluations at least 2 weeks apart. A Complete Response (CR) is defined as the complete disappearance of an M-protein and fewer than 5% bone marrow plasmacytosis. A Hematologic Very good partial response (VGPR) is defined as having a ≥ 90% reduction of M-protein from serum, a Urine M-spike to be ≤ 100 mg/24 hours, and a disappearance of soft tissue plasmacytomas. A Partial Response (PR) is defined as having a 50-89% reduction in the level of the serum monoclonal protein, a reduction in 24-hour urinary light chain excretion either by ≥90% or to <200 mg, and a ≥ 50% reduction in size of soft tissue plasmacytoma. | All 13 participants were evaluable for a response | Posted | Number | participants | Every 6 weeks from the first initiation of therapy up to 72 weeks |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Treatment (Kinase Inhibitor Therapy) | Patients receive oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hemoglobin decreased | Blood and lymphatic system disorders | MedDRA 10 | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hemoglobin decreased | Blood and lymphatic system disorders | MedDRA 10 | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Shaji Kumar, M.D. | Mayo Clinic Cancer Center | kumar.shaji@mayo.edu |
| ID | Term |
|---|---|
| D009101 | Multiple Myeloma |
| ID | Term |
|---|---|
| D054219 | Neoplasms, Plasma Cell |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D020141 | Hemostatic Disorders |
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| ID | Term |
|---|---|
| D000077210 | Sunitinib |
| ID | Term |
|---|---|
| D011758 | Pyrroles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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The distribution of duration of response will be estimated using the method of Kaplan-Meier.
| From the documentation of response until the date of progression |
| Toxicity | Assessed per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0. Included are the toxicities at least possibly related to the study drug. | From the time of first treatment to up to 30 days after the last day of study drug treatment |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Treatment (Kinase Inhibitor Therapy) |
Patients receive oral sunitinib malate once daily on days 1-42. Treatment repeats every 42 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
|
|
| Secondary | Event-free Survival | The distribution of progression-free survival will be estimated using the method of Kaplan-Meier. | Posted | Median | 95% Confidence Interval | months | Time from registration to progression or death due to any cause, assessed up to 3 years |
|
|
|
| Secondary | Duration of Response | The distribution of duration of response will be estimated using the method of Kaplan-Meier. | No analysis was done because there were no confirmed responses. | Posted | From the documentation of response until the date of progression |
|
|
| Secondary | Toxicity | Assessed per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0. Included are the toxicities at least possibly related to the study drug. | Posted | Number | participants | From the time of first treatment to up to 30 days after the last day of study drug treatment |
|
|
|
| 5 |
| 13 |
| 13 |
| 13 |
| Left ventricular dysfunction | Cardiac disorders | MedDRA 10 | Systematic Assessment |
|
| Vomiting | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Pain | General disorders | MedDRA 10 | Systematic Assessment |
|
| Pneumonia | Infections and infestations | MedDRA 10 | Systematic Assessment |
|
| Creatinine increased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Leukocyte count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Neutrophil count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Platelet count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Protein urine positive | Renal and urinary disorders | MedDRA 10 | Systematic Assessment |
|
| Renal failure | Renal and urinary disorders | MedDRA 10 | Systematic Assessment |
|
| Dyspnea | Respiratory, thoracic and mediastinal disorders | MedDRA 10 | Systematic Assessment |
|
| Hypoxia | Respiratory, thoracic and mediastinal disorders | MedDRA 10 | Systematic Assessment |
|
| Hypothyroidism | Endocrine disorders | MedDRA 10 | Systematic Assessment |
|
| Constipation | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Diarrhea | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Dyspepsia | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Ear, nose and throat examination abnormal | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Gastritis | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Nausea | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Oral pain | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Vomiting | Gastrointestinal disorders | MedDRA 10 | Systematic Assessment |
|
| Edema limbs | General disorders | MedDRA 10 | Systematic Assessment |
|
| Fatigue | General disorders | MedDRA 10 | Systematic Assessment |
|
| Fever | General disorders | MedDRA 10 | Systematic Assessment |
|
| Amylase increased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Leukocyte count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Lipase increased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Neutrophil count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Platelet count decreased | Investigations | MedDRA 10 | Systematic Assessment |
|
| Weight loss | Investigations | MedDRA 10 | Systematic Assessment |
|
| Anorexia | Metabolism and nutrition disorders | MedDRA 10 | Systematic Assessment |
|
| Serum calcium decreased | Metabolism and nutrition disorders | MedDRA 10 | Systematic Assessment |
|
| Bone pain | Musculoskeletal and connective tissue disorders | MedDRA 10 | Systematic Assessment |
|
| Dizziness | Nervous system disorders | MedDRA 10 | Systematic Assessment |
|
| Taste alteration | Nervous system disorders | MedDRA 10 | Systematic Assessment |
|
| Dyspnea | Respiratory, thoracic and mediastinal disorders | MedDRA 10 | Systematic Assessment |
|
| Hemorrhage nasal | Respiratory, thoracic and mediastinal disorders | MedDRA 10 | Systematic Assessment |
|
| Hand-and-foot syndrome | Skin and subcutaneous tissue disorders | MedDRA 10 | Systematic Assessment |
|
| Rash desquamating | Skin and subcutaneous tissue disorders | MedDRA 10 | Systematic Assessment |
|
| Skin hypopigmentation | Skin and subcutaneous tissue disorders | MedDRA 10 | Systematic Assessment |
|
| Hypertension | Vascular disorders | MedDRA 10 | Systematic Assessment |
|
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| D014652 |
| Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D010265 | Paraproteinemias |
| D001796 | Blood Protein Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D006474 | Hemorrhagic Disorders |
| D008232 | Lymphoproliferative Disorders |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D007211 |
| Indoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| Title | Measurements |
|---|---|
|