Ixabepilone in Treating Young Patients With Solid Tumors or Leukemia That Haven't Responded to Therapy

You may be eligible if

• DISEASE CHARACTERISTICS:
• Meets 1 of the following criteria:
• * Histologically confirmed solid tumor (closed to accrual as of 10/4/2007) that relapsed after or failed to respond to front-line curative therapy and for which no other potentially curative treatment options exist
• * Curative therapy may include surgery, radiotherapy, chemotherapy, or any combination of these modalities
• * Eligible tumor types include, but are not limited to, the following:
• * Rhabdomyosarcoma
• * Other soft tissue sarcomas
• * Ewing's sarcoma family of tumors
• * Osteosarcoma
• * Neuroblastoma
• * Wilms' tumor
• * Hepatic tumors
• * Germ cell tumors
• * Primary brain tumors
• * Histologic confirmation may be waived for brain stem or optic glioma
• * Diagnosis of relapsed or refractory leukemia
• * Patients with refractory or second or greater relapsed leukemia must have \> 25% blasts in the bone marrow (M3 bone marrow) with or without active extramedullary disease (except for leptomeningeal disease)
• * Relapsed after or failed to respond to frontline curative therapy and no other potentially curative therapy (e.g., radiotherapy, chemotherapy, or any combination of these modalities) exists
• * Patients with acute promyelocytic leukemia must be refractory to treatment with retinoic acid and arsenic trioxide
• * Patients with Philadelphia chromosome positive chronic myelogenous leukemia must be refractory to imatinib
• No active CNS leukemia (CNS3)
• PATIENT CHARACTERISTICS:
• Age:
• 2 to 18 (solid tumor patients \[closed to accrual as of 10/4/2007\])
• 1 to 21 (leukemia patients)
• Performance status:
• For patients age 11 to 21:
• * Karnofsky 50-100%
• For patients age 1 to 10:
• * Lansky 50-100%
• Life expectancy:
• Not specified
• Hematopoietic:
• Platelet count at least 100,000/mm\^3 (20,000/mm\^3 for leukemia patients)
• Hemoglobin ≥ 8.0 g/dL
• Hepatic:
• Bilirubin less than 1.5 times upper limit of normal (ULN)
• SGOT and SGPT less than 2.5 times ULN
• No hepatic dysfunction that would preclude study
• Renal:
• Creatinine normal for age OR
• Creatinine clearance at least 60 mL/min
• No renal dysfunction that would preclude study
• Other:
• No known severe prior hypersensitivity reaction to agents containing Cremophor EL
• No clinically significant unrelated systemic illness (e.g., serious infections or other organ dysfunction) that would preclude study
• No grade 2 or greater preexisting sensory neuropathy
• More than 2 month since prior and no concurrent evidence of graft vs host disease
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• PRIOR CONCURRENT THERAPY:
• Biologic therapy:
• Recovered from all therapy-related acute toxic effects (leukemia patients only)
• Prior epoetin alfa allowed
• At least 3 days since other prior colony-stimulating factors (e.g., filgrastim (G-CSF), sargramostim (GM-CSF), or interleukin-11 (IL-11))
• At least 6 months since prior bone marrow transplantation
• At least 2 months since prior stem cell transplantation or rescue (leukemia patients)
• At least 7 days since prior therapy with a biological agent and hematopoietic growth factor with the exception of erythropoietin
• More than 3 weeks since prior monoclonal antibody therapy (leukemia patients only)
• No concurrent GM-CSF or IL-11
• No concurrent immunotherapy
• Chemotherapy:
• See Disease Characteristics
• Recovered from all therapy-related acute toxic effects (leukemia patients only)
• At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas)
• No other concurrent anticancer chemotherapy
• Endocrine therapy:
• Concurrent corticosteroids allowed for the control of symptoms related to tumor-associated edema in patients with brain tumors
• Patients with brain tumors must be on a stable or tapering dose of corticosteroids for 7 days before baseline scan is performed for the purpose of assessing response to study therapy
• Must be on a stable or tapering dose of corticosteroids for 7 days prior to study entry (leukemia patients only)
• Radiotherapy:
• See Disease Characteristics
• Recovered from all therapy-related acute toxic effects (leukemia patients only)
• At least 4 weeks since prior radiotherapy
• More than 2 weeks since prior local palliative radiotherapy (leukemia patients only)
• More than 3 months since prior total-body irradiation, craniospinal radiotherapy, or radiotherapy to ≥50% of the pelvis (leukemia patients only)
• More than 6 weeks since prior other substantial bone marrow radiotherapy (leukemia patients only)
• No prior extensive radiotherapy (e.g., craniospinal irradiation, total body irradiation, or radiotherapy to more than half of the pelvis)
• No concurrent anticancer radiotherapy
• Surgery:
• See Disease Characteristics
• Other:
• Recovered from prior therapy
• At least 30 days since any prior investigational anticancer therapy
• At least 1 week since prior known inhibitors of CYP3A4, including any of the following:
• * Antibiotics (i.e., clarithromycin, erythromycin, or troleandomycin)
• * Anti-HIV agents (i.e, delaviridine, nelfinavir, amprenavir, ritonavir, idinavir, saquinavir, or lopinavir)
• * Anti-fungals (i.e., itraconazole, ketoconazole, fluconazole \[doses \> 3mg/kg/day\], or voriconazole)
• * Anti-depressants (i.e., nefaxodone or fluovoxamine)
• * Calcium channel blockers (i.e., verapamil or diltiazem)
• * Anti-emetics (i.e., aprepitant \[Emend®\])
• * Miscellaneous agents (i.e., amiodarone)
• * Grapefruit juice
• No other concurrent investigational agents
• No concurrent St. John's Wort
• No concurrent known inhibitors of CYP3A4, including grapefruit juice
• Concurrent other agents inducing CYP3A4 allowed