Sorafenib in Treating Young Patients With Relapsed or Refractory Solid Tumors or Leukemia

A Phase I/II Study of the Raf Kinase and Receptor Tyrosine Kinase Inhibitor Sorafenib (BAY 43-9006, NSC# 724772) in Children With Refractory Solid Tumors or Refractory Leukemias

This phase I/II trial is studying the side effects and best dose of sorafenib in treating young patients with relapsed or refractory solid tumors or leukemia. Sorafenib 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.

Study Overview

• Status: Completed
• Conditions: Juvenile Myelomonocytic Leukemia; Recurrent Disease; Recurrent Childhood Acute Lymphoblastic Leukemia; Recurrent Childhood Acute Myeloid Leukemia; Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive; Childhood Solid Neoplasm; Chronic Myelogenous Leukemia, BCR-ABL1 Positive; Philadelphia Chromosome Negative, BCR-ABL1 Positive Chronic Myelogenous Leukemia; Blastic Phase; Childhood Acute Promyelocytic Leukemia With PML-RARA
• Intervention / Treatment: Other: Laboratory Biomarker Analysis; Other: Pharmacological Study; Drug: Sorafenib Tosylate

Detailed Description

PRIMARY OBJECTIVES:

I. Determine the maximum-tolerated dose (MTD) and recommended phase II dose of sorafenib in pediatric patients with relapsed or refractory solid tumors.

II. Determine whether pediatric patients with relapsed or refractory leukemia can tolerate the MTD of sorafenib for solid tumors.

III. Determine the tolerability, active N-oxide metabolite, pharmacodynamics, and activity of sorafenib a the MTD in a subset of patients with acute myeloid leukemia (AML) and FLT3-ITD mutation.

IV. Determine the toxicities of this drug in these patients. V. Determine the pharmacokinetics of this drug in these patients.

SECONDARY OBJECTIVES:

I. Determine, preliminarily, the antitumor activity of this drug within the confines of a phase I trial.

II. Assess the biologic effect of sorafenib on circulating endothelial cells (CEC), circulating CEC precursors (CECP), VEGF, and VEGF-2 in peripheral blood.

III. Assess the gene expression, proteomic profile, and ERK phosphorylation in blasts of patients with refractory leukemia treated with this regimen.

IV. Assess the effect of sorafenib on solid tumor vascularity and tumor blood flow using dynamic contrast-enhanced MRI (DEMRI) in patients with measurable soft tissue tumors.

V. Analyze tumor samples and leukemic blasts for the presence of ras, raf, or FLT3 (leukemias) mutations.

VI. Analyze the plasma inhibitory activity for FLT3 phosphorylation in peripheral blood of patients with AML and FLT3-ITD mutation.

VII. Determine the tolerability, pharmacokinetics of sorafenib and sorafenib?s active N-oxide metabolite, pharmacodynamics, and activity of sorafenib administered at the MTD for refractory leukemias in a subset of patients with AML and FLT3-ITD mutation.

VIII. Analyze the plasma inhibitory activity for FLT3 phosphorylation in peripheral blood samples obtained at the time of PK studies in patients with FLT3-ITD mutation AML.

OUTLINE: This is a dose-escalation, multicenter study. Patients are stratified according to diagnosis (malignant solid tumor vs leukemia).

STRATUM I(REFRACTORY SOLID TUMOR PATIENTS): Patients receive oral sorafenib twice daily on days 1-28. Treatment repeats every 28 days for up to 24 courses in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of sorafenib until the maximum-tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity (DLT). Once the MTD is determined, up to 6 additional patients under 12 years of age may be treated at the MTD. The MTD dose level is also expanded to enroll up to 6 patients with refractory leukemia.

STRATUM II (REFRACTORY LEUKEMIA PATIENTS): A cohort of 3-6 patients with leukemia receives treatment as in stratum 1 at the MTD determined in stratum 1. If 2 of 3 or 2 of 6 patients experience a DLT at the solid tumor MTD, sorafenib is reduced by one dose level. The leukemia MTD is defined as the dose at which < 1/3 of patients experience DLT during course 1 of treatment.

STRATUM III (ACUTE MYELOID LEUKEMIA AND FLT3-ITD MUTATION PATIENTS): Patients receive sorafenib as in stratum 1 at the MTD determined in stratum 2. Patients undergo blood sample collection for pharmacokinetics, pharmacodynamics (in leukemia blasts only), circulating endothelial cells (CEC), circulating CEC precursors (CECP), VEGF and VEGF-2 , gene expression, proteomic profile, ERK phosphorylation, and FLT3 phosphorylation activity. Tumor tissue samples may also be analyzed for the presence of ras, raf, or FLT3.

After completion of study treatment, patients are followed periodically.

• Study Type: Interventional
• Enrollment (Actual): 70
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• Canada
  • Ontario
    • Toronto, Ontario, Canada, M5G 1X8
      • Hospital for Sick Children
  • Quebec
    • Montreal, Quebec, Canada, H3T 1C5
      • Centre Hospitalier Universitaire Sainte-Justine
• United States
  • Alabama
    • Birmingham, Alabama, United States, 35233
      • University of Alabama at Birmingham Cancer Center
  • California
    • Orange, California, United States, 92868
      • Children's Hospital of Orange County
    • Palo Alto, California, United States, 94304
      • Lucile Packard Children's Hospital Stanford University
  • District of Columbia
    • Washington, District of Columbia, United States, 20010
      • Children's National Medical Center
  • Illinois
    • Chicago, Illinois, United States, 60611
      • Lurie Children's Hospital-Chicago
  • Indiana
    • Indianapolis, Indiana, United States, 46202
      • Indiana University/Melvin and Bren Simon Cancer Center
    • Indianapolis, Indiana, United States, 46202
      • Riley Hospital for Children
  • Maryland
    • Bethesda, Maryland, United States, 20892
      • National Institutes of Health Clinical Center
  • Massachusetts
    • Boston, Massachusetts, United States, 02215
      • Dana-Farber Cancer Institute
  • Michigan
    • Ann Arbor, Michigan, United States, 48109
      • C S Mott Children's Hospital
  • Minnesota
    • Minneapolis, Minnesota, United States, 55455
      • University of Minnesota/Masonic Cancer Center
  • Missouri
    • Saint Louis, Missouri, United States, 63110
      • Washington University School of Medicine
  • New York
    • New York, New York, United States, 10032
      • Columbia University/Herbert Irving Cancer Center
    • Syracuse, New York, United States, 13210
      • State University of New York Upstate Medical University
  • Ohio
    • Cincinnati, Ohio, United States, 45229
      • Cincinnati Children's Hospital Medical Center
  • Oregon
    • Portland, Oregon, United States, 97239
      • Oregon Health and Science University
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19104
      • Children's Hospital of Philadelphia
    • Pittsburgh, Pennsylvania, United States, 15224
      • Children's Hospital of Pittsburgh of UPMC
  • Tennessee
    • Memphis, Tennessee, United States, 38105
      • St. Jude Children's Research Hospital
  • Texas
    • Dallas, Texas, United States, 75390
      • UT Southwestern/Simmons Cancer Center-Dallas
    • Houston, Texas, United States, 77030
      • Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
  • Washington
    • Seattle, Washington, United States, 98105
      • Seattle Children's Hospital
  • Wisconsin
    • Milwaukee, Wisconsin, United States, 53226
      • Children's Hospital of Wisconsin

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 2 years to 21 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Diagnosis of 1 of the following:

  • Histologically confirmed malignant solid tumor at original diagnosis or relapse

    • Measurable or evaluable disease by CT scan or MRI

  • Histologically confirmed leukemia, including 1 of the following:

    • Acute lymphoblastic leukemia (ALL)

      • Greater than 25% blasts in the bone marrow (M3 bone marrow)

    • Acute myeloid leukemia (AML)

      • Greater than 25% blasts in the bone marrow (M3 bone marrow)

    • AML and FLT3-ITD mutation

      • Patients must have ? 5% blasts in the bone marrow
      • Active extramedullary disease (except leptomeningeal disease) allowed

    • Juvenile myelomonocytic leukemia (JMML) meeting the following criteria:

      • Peripheral blood monocytosis > 1,000/mm^3
      • Blasts (including promonocytes) are < 20% of the WBCs in the blood and of the nucleated bone marrow cells
      • No Philadelphia chromosome (Ph) or BCR/ABL fusion gene

      • Has ? 2 of the following additional diagnostic criteria:

        • Hemoglobin F increased for age
        • Immature granulocytes in the peripheral blood
        • WBC > 10,000/mm^3
        • Clonal chromosomal abnormality (e.g., may be monosomy 7)
        • Sargramostim (GM-CSF) hypersensitivity of myeloid progenitors in vitro

    • Chronic myelogenous leukemia (CML) in blast crisis

      • Greater than 25% blasts in the bone marrow (M3 bone marrow)
      • Patients with Ph-positive CML must be refractory to imatinib mesylate

• Relapsed or refractory disease

  • Patients with acute promyelocytic leukemia (APL) must be refractory to treatment with tretinoin and arsenic trioxide
• Standard curative therapies or therapies proven to prolong survival with an acceptable quality of life do not exist
• Active extramedullary disease, except active leptomeningeal leukemia, allowed
• No brain tumors or known brain metastases
• Karnofsky performance status (PS) 50-100% (for patients > 10 years of age)
• Lansky PS 50-100% (for patients ? 10 years of age)

• Patients with solid tumors must have adequate bone marrow function, as defined by the following:

  • Absolute neutrophil count ? 1,000/mm^3
  • Platelet count ? 75,000/mm^3 (transfusion independent)
  • Hemoglobin ? 8.0 g/dL (red blood cell [RBC] transfusions allowed)

• Patients with leukemia may have abnormal blood counts but must meet the following criteria:

  • Platelet count ? 20,000/mm^3 (platelet transfusions allowed)
  • Hemoglobin ? 8.0 g/L (RBC transfusions allowed)

• Patients with acute myeloid leukemia and FLT3-ITD mutation

  • Platelet count ? 20,000/mm^3
• Lipase and amylase normal

• Creatinine clearance or radioisotope glomerular filtration rate ? 70 mL/min OR creatinine normal based on age as follows:

  • No greater than 0.8 mg/dL (for patients 5 years of age and under)
  • No greater than 1.0 mg/dL (for patients 6-10 years of age)
  • No greater than 1.2 mg/dL (for patients 11-15 years of age)
  • No greater than 1.5 mg/dL (for patients over 15 years of age)

• Patients with solid tumors must meet the following criteria:

  • Bilirubin normal for age
  • ALT normal for age (for the purpose of this study, the upper limit of normal [ULN] for ALT is 45 ?/L)
  • Serum albumin ? 2 g/dL

• Patients with leukemia must meet the following criteria:

  • Bilirubin (sum of conjugated + unconjugated) ? 1.5 times ULN for age
  • ALT ? 5.0 times ULN for age (? 225 ?/L) (for the purpose of this study, the ULN for ALT is 45 ?/L)
  • Serum albumin ? 2 g/dL
• Albumin ? 2 g/dL
• PT, PTT, and INR normal (for patients on prophylactic anticoagulation)
• No evidence of dyspnea at rest
• No exercise intolerance
• Pulse oximetry >94% on room air, if there is clinical indication for determination
• Diastolic blood pressure ? the 95th percentile for age and gender (height included for AML and FLT3-ITD mutation patients)
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No uncontrolled infection
• Able to swallow tablets
• No evidence of bleeding diathesis
• No other medical condition or situation that would preclude study compliance
• No known Gilbert syndrome
• Fully recovered from prior chemotherapy, immunotherapy, or radiotherapy (for patients with solid tumors)
• Recovered from the non-hematologic toxic effects of all prior therapy (for patients with leukemia)
• Recovered from acute non-hematologic toxic effects of all prior anti-cancer chemotherapy (for patients with AML and FLT3-ITD mutation)
• At least 7 days since prior hematopoietic growth factors
• At least 7 days since prior biologic agents
• At least 2 weeks since prior local palliative radiotherapy (small port)
• At least 3 months since prior total-body irradiation, craniospinal radiotherapy, or radiation to ? 50% of the pelvis
• At least 6 weeks since other prior substantial bone marrow radiation (e.g., skull, spine, pelvis, ribs)

• At least 3 months since prior stem cell transplantation or rescue (for patients with solid tumors)

  • No evidence of active graft-vs-host disease
• At least 3 months since prior myeloablative therapy followed by bone marrow or stem cell transplantation (for patients with leukemia)

• At least 3 weeks since prior myelosuppressive chemotherapy (6 weeks for nitrosoureas) (for patients with solid tumors)

  • At least 24 hours since prior nitrosoureas (for patients with AML and FLT3-ITD mutation)
• At least 2 weeks since prior chemotherapy (for patients with leukemia)
• At least 3 weeks since prior monoclonal antibody therapy
• No prior sorafenib
• No other concurrent investigational drugs

• No other concurrent anticancer agents or therapies, including chemotherapy, radiotherapy, immunotherapy, or biologic therapy

  • Concurrent maintenance-like chemotherapy for patients with AML and FLT3-ITD mutation allowed

• No concurrent administration of any of the following:

  • Cytochrome P450 enzyme-inducing antiepileptic drugs (e.g., phenytoin, carbamazepine, or phenobarbital)
  • Rifampin
  • Grapefruit juice
  • Hypericum perforatum (St. John wort)

• No concurrent therapeutic anticoagulation

  • Concurrent prophylactic anticoagulation (e.g., low-dose warfarin) of venous or arterial access devices allowed provided the requirements for PT, INR, or PTT are met

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment (sorafenib tosylate); Patients receive oral sorafenib twice daily on days 1-28. Treatment repeats every 28 days for up to 24 courses in the absence of disease progression or unacceptable toxicity.	Other: Laboratory Biomarker Analysis; Correlative studies; Other: Pharmacological Study; Correlative studies; Drug: Sorafenib Tosylate; Given orally; Other Names: BAY 54-9085; Nexavar; BAY 43-9006 Tosylate; sorafenib

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Patients With Treatment-related Dose Limiting Toxicity in Cycle 1 by Dose Level	Number of patients with treatment-related dose limiting toxicities in cycle 1, as defined by study protocol, stratified by dose level.	Up to 28 days
Number of Patients With Treatment-related Adverse Events	Number of patients with treatment-related adverse events stratified by dose level through study completion.	Up to 2 years
Area Under the Plasma Concentration Versus Time Curve (AUC) of Sorafenib	Area under the plasma concentration versus time curve (AUC) of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with refractory solid tumors or leukemias.	During cycle 1 or cycle 2 after at least 14 consecutive days of sorafenib administration Pre-dose, 0.5, 1, 2, 3, 5, 8 hours post dose
Clearance (Cl) of Sorafenib	Clearance of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with refractory solid tumors or leukemias.	During cycle 1 or cycle 2 after at least 14 consecutive days of sorafenib administration Pre-dose, 0.5, 1, 2, 3, 5, 8 hours post dose
Half-life of Sorafenib	Half-life of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with refractory solid tumors or leukemias.	During cycle 1 or cycle 2 after at least 14 consecutive days of sorafenib administration Pre-dose, 0.5, 1, 2, 3, 5, 8 hours post dose
Maximum Serum Concentration (Cmax) of Sorafenib	Maximum serum concentration (Cmax) of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with refractory solid tumors or leukemias.	During cycle 1 or cycle 2 after at least 14 consecutive days of sorafenib administration Pre-dose, 0.5, 1, 2, 3, 5, 8 hours post dose
Number of Patients With Treatment-related Dose Limiting Toxicities in Later Cycles by Dose Level	Number of patients with treatment-related dose limiting toxicities in later cycles, as defined by study protocol, stratified by dose level.	Up to 2 years
Area Under the Plasma Concentration Versus Time Curve (AUC) of Sorafenib	Area under the plasma concentration versus time curve (AUC) of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with AML and FLT3-ITD mutation.	8 hours post dose on day 1 of cycle 1
Clearance (Cl) of Sorafenib	Clearance of Sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with AML and FLT3-ITD mutation.	8 hours post dose on day 1 of cycle 1
Half-life of Sorafenib	Half-life of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with AML and FLT3-ITD mutation.	8 hours post dose on day 1 of cycle 1
Volume of Distribution at Steady State (Vss) of Sorafenib	Volume of distribution at steady state (Vss) of sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with refractory solid tumors, leukemia, or AML and FLT3-ITD mutation.	8 hours post dose on day 1 of cycle 1
Maximum Serum Concentration (Cmax) of Sorafenib	Maximum serum concentration (Cmax) of Sorefenib administered orally as tablets, BID approximately every 12 hours for cycles of 28 days with no rest period between cycles to children with AML and FLT3-ITD mutation.	8 hours post dose on day 1 of cycle 1

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Patients Who Respond Using RECIST Criteria	Frequency (%) of patients with Partial Response (PR) or Complete Response (CR) using the RECIST criteria by study part and dose level	Up to 2 years
Mean Concentration of VEGF2	Mean concentration of VEGF2 in peripheral blood sample.	28 days
Pharmacodynamics (PD) Blood Flow Part C	Pharmacodynamics: tumor blood flow in patients with AML and FLT3-ITD mutation using dynamic contrast enhanced MRI (DEMRI) (Part C).	1 week prior to enrollment, then every 28 days
Number of Patients With DEMRI	Assess effect on tumor blood flow via DEMRI in patients with measurable soft tissue tumors.	Up to 2 years
Leukemia Mutations	Analyze tumor samples and leukemic blasts from patients entered on this study for the presence of ras, raf, or FLT3 (leukemia) mutations.	1 week prior to enrollment
Plasma Inhibitory Activity (PIA)	Analyze the plasma inhibitory activity (PIA) for FLT3 phosphorylation in peripheral blood samples obtained at the time of PK studies in patients with FLT3-ITD mutation AML (Part C).	1 week prior to enrollment and then every 28 days

Collaborators and Investigators

• Sponsor: National Cancer Institute (NCI)
• Investigators: Principal Investigator: Brigitte C Widemann, COG Phase I Consortium

Study record dates

Study Major Dates

• Study Start (Actual): May 30, 2006
• Primary Completion (Actual): March 16, 2012
• Study Completion (Actual): December 10, 2012

Study Registration Dates

• First Submitted: September 30, 2011
• First Submitted That Met QC Criteria: September 30, 2011
• First Posted (Estimate): October 3, 2011

Study Record Updates

• Last Update Posted (Actual): February 2, 2021
• Last Update Submitted That Met QC Criteria: January 13, 2021
• Last Verified: January 1, 2021

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Immune System Diseases; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Disease Attributes; Bone Marrow Diseases; Hematologic Diseases; Myeloproliferative Disorders; Myelodysplastic-Myeloproliferative Diseases; Leukemia, Lymphoid; Chromosome Aberrations; Translocation, Genetic; Leukemia, Myeloid, Acute; Leukemia; Leukemia, Myeloid; Recurrence; Leukemia, Myelomonocytic, Juvenile; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Leukemia, Promyelocytic, Acute; Philadelphia Chromosome; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antineoplastic Agents; Protein Kinase Inhibitors; Sorafenib
• Other Study ID Numbers: NCI-2009-00358 (Registry Identifier: CTRP (Clinical Trial Reporting Program)); U01CA097452 (U.S. NIH Grant/Contract); 06-C-0233; CDR0000483040; COG-ADVL0413; NCI-06-C-0233; 060233; ADVL0413 (Other Identifier: CTEP)