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

A Phase I Study of High-dose Pyrazoloacridine (PZA) (NSC 366140) Supported With Autologous Hematopoietic Stem Cell Rescue in Children With Recurrent or Resistant Neuroblastoma (IND # 36325)

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.

Study Overview

• Status: Terminated
• Conditions: Recurrent Neuroblastoma; Disseminated Neuroblastoma
• Intervention / Treatment: Other: laboratory biomarker analysis; Other: pharmacological study; Biological: filgrastim; Drug: pyrazoloacridine; Procedure: autologous bone marrow transplantation; Procedure: peripheral blood stem cell transplantation

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.

• Study Type: Interventional
• Enrollment (Actual): 42
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • California
    • Los Angeles, California, United States, 90027-6016
      • New Approaches to Neuroblastoma Treatment (NANT)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 year to 30 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 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.	Other: laboratory biomarker analysis; Correlative studies; Other: pharmacological study; Correlative studies; Other Names: pharmacological studies; Biological: filgrastim; Given IV or SC; Other Names: G-CSF; Neupogen; Drug: pyrazoloacridine; Given IV; Other Names: PZA; Procedure: autologous bone marrow transplantation; Undergo autologous bone marrow transplantation; Other Names: ABMT; bone marrow transplantation, autologous; transplantation, autologous bone marrow; Procedure: peripheral blood stem cell transplantation; Undergo peripheral blood stem cell transplantation; Other Names: PBPC transplantation; PBSC transplantation; peripheral blood progenitor cell transplantation; transplantation, peripheral blood stem cell
Experimental: 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.	Other: laboratory biomarker analysis; Correlative studies; Other: pharmacological study; Correlative studies; Other Names: pharmacological studies; Biological: filgrastim; Given IV or SC; Other Names: G-CSF; Neupogen; Drug: pyrazoloacridine; Given IV; Other Names: PZA; Procedure: autologous bone marrow transplantation; Undergo autologous bone marrow transplantation; Other Names: ABMT; bone marrow transplantation, autologous; transplantation, autologous bone marrow; Procedure: peripheral blood stem cell transplantation; Undergo peripheral blood stem cell transplantation; Other Names: PBPC transplantation; PBSC transplantation; peripheral blood progenitor cell transplantation; transplantation, peripheral blood stem cell

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Maximum tolerated dose determined by dose-limiting toxicities by NCI Common Toxicity Criteria	28 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Survival		Up to 4 years
Time to engraftment (hematopoietic recovery)	Will be summarized with tables and with Kaplan-Meier plots.	Up to 4 years
Response by RECIST or MIBG-scans		28 days
Time to progression		Up to 4 years
Time to failure		Time from start of treatment until death for any cause or disease progression, assessed up to 4 years
Pharmacokinetic (such as AUC, Cmax, Tmax, and clearance in the plasma) determinations	Will be summarized by dose level with simple summary statistics: means (possibly after transformation) or medians, ranges, and standard deviations.	3, 24, 72,and 192 hours after starting infusion

Collaborators and Investigators

• Sponsor: National Cancer Institute (NCI)
• Investigators: Principal Investigator: Anna Butturini, New Approaches to Neuroblastoma Treatment (NANT)

Study record dates

Study Major Dates

• Study Start: December 1, 2002
• Primary Completion (Actual): March 1, 2007

Study Registration Dates

• First Submitted: February 5, 2003
• First Submitted That Met QC Criteria: February 5, 2003
• First Posted (Estimate): February 6, 2003

Study Record Updates

• Last Update Posted (Estimate): April 9, 2013
• Last Update Submitted That Met QC Criteria: April 8, 2013
• Last Verified: April 1, 2013

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neoplasms, Glandular and Epithelial; Neoplasms, Neuroepithelial; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms, Nerve Tissue; Neuroectodermal Tumors, Primitive; Neuroectodermal Tumors, Primitive, Peripheral; Neuroblastoma; Antineoplastic Agents; NSC 366140
• Other Study ID Numbers: NCI-2012-03166; P01CA081403 (U.S. NIH Grant/Contract); NANT N2002-01; CHLA-NANT-N2002-01; CDR0000269644