Pyrazoloacridine and Stem Cell or Bone Marrow Transplantation in Treating Young Patients With High-Risk Neuroblastoma

NCT ID: NCT00053950

Last Updated: 2013-04-09

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 42 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-12-31

Brief Summary

This phase I trial is studying the side effects and best dose of pyrazoloacridine given together with peripheral stem cell or bone marrow transplantation in treating young patients with high-risk neuroblastoma. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell or bone marrow transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine the maximum tolerated dose (MTD) of PZA given as a single prolonged infusion (>= 6 hours) with autologous hematopoietic stem cell (aHSC) support to children with high risk neuroblastoma with recurrent or refractory disease.

II. To determine the dose limiting toxicity (DLT) of PZA given on this schedule.

III. To characterize the pharmacokinetics of PZA given on this schedule.

SECONDARY OBJECTIVES:

I. To obtain preliminary data on the antitumor activity of PZA within the confines of a Phase I study.

II. To determine the TP53 mutation status of tumor cells in bone marrow if > 10% are present; to evaluate expression of p53 and MDM2 proteins by flow cytometry if >= 0.1% to < 10% are present at study entry.

OUTLINE: This is a two-stage, dose-escalation study.

Patients without adequate cryopreserved hematopoietic stem cells undergo peripheral blood stem cell harvest or bone marrow harvest for autologous stem cells at least 2 weeks before study therapy.

Patients receive high-dose pyrazoloacridine (PZA) IV on day 0.

Cohort 1: Groups of 3-6 patients receive escalating doses of PZA at a fixed infusion time until the maximum tolerated dose (MTD) is determined.

Cohort 2: Groups of 3-6 patients receive PZA at the dose/hour established in cohort I at escalating infusion times until another MTD is determined.

In both cohorts the MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients receive filgrastim (G-CSF) IV or subcutaneously beginning on day 4 and continuing until blood counts recover. Patients also undergo reinfusion of stem cells over 15-30 minutes on day 4 as needed per protocol.

Patients are followed at days 28-35, every 3 months for 3 years, and then every 6 months thereafter.

Conditions

Disseminated Neuroblastoma; Recurrent Neuroblastoma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort I

Groups of 3-6 patients receive escalating doses of PZA at a fixed infusion time until the MTD is determined. In both cohorts the MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Patients receive G-CSF IV or subcutaneously beginning on day 4 and continuing until blood counts recover. Patients also undergo reinfusion of stem cells over 15-30 minutes on day 4 as needed per protocol.

Group Type: EXPERIMENTAL

pyrazoloacridine

Intervention Type: DRUG

Given IV

filgrastim

Intervention Type: BIOLOGICAL

Given IV or SC

autologous bone marrow transplantation

Intervention Type: PROCEDURE

Undergo autologous bone marrow transplantation

peripheral blood stem cell transplantation

Intervention Type: PROCEDURE

Undergo peripheral blood stem cell transplantation

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

pharmacological study

Intervention Type: OTHER

Correlative studies

Cohort II

Groups of 3-6 patients receive PZA at the dose/hour established in cohort I at escalating infusion times until another MTD is determined. In both cohorts the MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Patients receive G-CSF IV or subcutaneously beginning on day 4 and continuing until blood counts recover. Patients also undergo reinfusion of stem cells over 15-30 minutes on day 4 as needed per protocol.

Group Type: EXPERIMENTAL

pyrazoloacridine

Intervention Type: DRUG

Given IV

filgrastim

Intervention Type: BIOLOGICAL

Given IV or SC

autologous bone marrow transplantation

Intervention Type: PROCEDURE

Undergo autologous bone marrow transplantation

peripheral blood stem cell transplantation

Intervention Type: PROCEDURE

Undergo peripheral blood stem cell transplantation

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

pharmacological study

Intervention Type: OTHER

Correlative studies

Interventions

pyrazoloacridine

Given IV

Intervention Type: DRUG

filgrastim

Given IV or SC

Intervention Type: BIOLOGICAL

autologous bone marrow transplantation

Undergo autologous bone marrow transplantation

Intervention Type: PROCEDURE

peripheral blood stem cell transplantation

Undergo peripheral blood stem cell transplantation

Intervention Type: PROCEDURE

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

pharmacological study

Correlative studies

Intervention Type: OTHER

Other Intervention Names

PZA; G-CSF; Neupogen; ABMT; bone marrow transplantation, autologous; transplantation, autologous bone marrow; PBPC transplantation; PBSC transplantation; peripheral blood progenitor cell transplantation; transplantation, peripheral blood stem cell; pharmacological studies

Eligibility Criteria

Inclusion Criteria

• Patients must have a diagnosis of neuroblastoma (ICD-O morphology 9500/3) verified by histology and/or demonstration of clumps of tumor cells in bone marrow with elevated urinary catecholamine metabolites
• Patients must meet one of the two following disease status criteria to enter on study;

• Current or prior progressive disease (PD) by INRC criteria
• Either mixed response (MR) or no response (NR) by INRC criteria following completion of minimum of 4 courses of induction therapy
• Patients meeting disease status criteria in either category A or B must also have at least one of the following sites of disease present to enter on study:

• At least one tumor lesion on CT or MRI scan that is >= 20mm in at least one dimension (spiral CT lesion must be >= 10mm in at least one dimension)
• MIBG scan with positive uptake at a minimum of one site
• Bone marrow disease documented by standard histology of bilateral bone marrow aspirate and biopsy specimens
• Patients > 16 years of age: Karnofsky >= 50%; Patients =< 16 years of age: Lansky >= 50%; patients who are unable to walk because of paralysis, but who are up in a wheelchair will be considered ambulatory for the purpose of assessing the performance score; life expectancy must be >= 2 months for all patients
• Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study

• Chemotherapy and/or biologics: Must not have received treatment within 3 weeks of entry onto this study (4 weeks if prior nitrosureas
• Radiation: At least 4 weeks since last dose of radiation therapy to at least one lesion being used as criteria for study eligibility; only 2 weeks must elapse since the last dose of radiation (small port) to a lesion not used for study eligibility; at least 6 months must have elapsed since the last dose of prior craniospinal XRT and radiation to >= 50% of the pelvis or TBI
• Stem Cell Transplant (SCT): >= 9 months must have elapsed since autologous hematopoietic stem cell transplant (aHSCT)
• Prior MIBG therapy: At least 12 weeks must have elapsed since treatment with therapeutic doses of MIBG
• Study specific limitations on prior therapy: patients who have a history of allogeneic HSCT are not eligible
• Growth factor(s): At least 7 days since the last dose of any myeloid growth factor was given
• Any patient considered for this protocol must meet the following criteria for minimum number of autologous stem cells sufficient to rescue hematopoiesis; a combination of products may be used to meet this requirement
• All stem cell products infused on this protocol must meet the following criteria for tumor analysis: No tumor cells detectable by immunocytology OR for patients who had a PBSC collection done previously and no immunocytological testing was done on the product at the time of collection: This product may be used for infusion on this study if the patient's bilateral bone marrow aspirate and biopsy specimens can be shown to be tumor free by standard histology within 4 weeks of PBSC collection
• Glomerular filtration rate (GFR) using blood draw method or 12 hour urine collection for creatinine clearance >= 100 ml/min/1.73 m^2
• Serum creatinine =< 1.5 x upper limit of normal for age
• Normal ejection fraction (>= 55%) documented by echocardiogram or radionuclide MUGA evaluation OR normal fractional shortening (>= 27%) documented by echocardiogram
• Total bilirubin < 1.5 x upper limit of normal
• AST/ALT =< 3 x upper limit of normal
• Platelets >= 75,000/uL (transfusion independent)
• Hemoglobin >= 8 g/dl (transfusion allowed)
• Because evaluation of hematopoietic toxicity is essential to this study, the same criteria will be applied to patients with tumor infiltration of the bone marrow
• Normal lung function as manifested by no dyspnea at rest and no oxygen requirement

Exclusion Criteria

• No patients who are pregnant or lactating will be allowed to enter on study; pregnancy tests must be obtained in females who are post-menarchal; males and females of reproductive potential may not participate unless they have agreed to use an effective method of contraception while receiving therapy
• Patients with active infections requiring intravenous antivirals, antibiotics, or antifungals; patients on prolonged antifungal therapy are still eligible if they are culture negative and biopsy negative in suspected residual radiographic lesions and they meet other organ function criteria; patients who are known HIV seropositive with stable disease and lack of major health problems who are not on anti-retroviral therapy, may be eligible at the discretion of the Study Chair
• Prior treatment with Pyrazoloacridine (PZA)
• Prior history of allogeneic HSCT
• Neurologic Exclusions:

• Acute or chronic CNS disease
• History of seizures
• History of cerebral bleeding or stroke
• CNS parenchymal metastases as documented by head CT with contrast or head MRI with gadolinium performed within 30 days of study entry. Patients with epidural metastases causing mass effect on the brain are also excluded (skull metastases are allowed provided they are not associated with intracranial disease compressing or displacing the brain

• Minimum Eligible Age: 1 Year
• Maximum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Anna Butturini

Role: PRINCIPAL_INVESTIGATOR

New Approaches to Neuroblastoma Treatment (NANT)

Locations

New Approaches to Neuroblastoma Treatment (NANT)

Los Angeles, California, United States

Countries

United States

Other Identifiers

NANT N2002-01

Identifier Type: -

Identifier Source: secondary_id

P01CA081403

Identifier Type: NIH

Identifier Source: secondary_id

View Link

CHLA-NANT-N2002-01

Identifier Type: -

Identifier Source: secondary_id

CDR0000269644

Identifier Type: -

Identifier Source: secondary_id

NCI-2012-03166

Identifier Type: -

Identifier Source: org_study_id