Comparison of Filgrastim and Filgrastim SD/01in Boosting White Cell Counts After Intensive Chemotherapy

Sponsor

National Cancer Institute (NCI) (NIH)

Overall Status

Completed

CT.gov ID

NCT00004853

Collaborator

(none)

Enrollment

Location

Arms

110.6

Duration (Months)

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Filgrastim (granulocyte colony-stimulating factor), which is administered by daily subcutaneous injection after cytotoxic chemotherapy, shortens the duration of chemotherapy-induced neutropenia and lowers the risk of infection. In children treated with dose-intensive chemotherapy, filgrastim reduces the duration of severe neutropenia and, as a result, has become a standard component of the treatment regimen. Filgrastim-SD/01 (AMGEN), which is produced by PEGylation of the amino-terminus of filgrastim, is a sustained duration form of granulocyte colony-stimulating factor. In phase I and phase II trials in adults, a single dose of Filgrastim-SD/01 appears to be equivalent to daily dosing of filgrastim in enhancing neutrophil recovery and has a comparable adverse event profile.

Dose-intensive vincristine/cyclophosphamide/doxorubicin (VDoxC) alternating with ifosfamide/etoposide (IE) has become standard therapy for children and adolescents with Ewing's sarcoma and other sarcomas treated at the POB/NCI and other cancer centers within the US. Supportive care measures used in children who are treated with this regimen include mesna to prevent oxazaphosphorine urotoxicity, dexrazoxane to reduce doxorubicin cardiotoxicity, and filgrastim to shorten the duration of neutropenia. The purpose of this randomized open label trial is to compare the tolerance, toxicity, and therapeutic effects of Filgrastim-SD/01 given as a single injection after chemotherapy to daily subcutaneous filgrastim in patients with newly diagnosed sarcoma. The pharmacokinetics of Filgrastim-SD/01 will also be compared to the pharmacokinetics of filgrastim. This trial will also be a platform for performing biological studies of these tumors and for detailed cardiac studies. High-risk patients who are treated on this front line trial and respond will also be candidates for a planned transplant protocol. A total of 34 patients (17 patients per treatment arm) will be entered onto the trial.

Condition or Disease	Intervention/Treatment	Phase
Ewing's Sarcoma Rhabdomyosarcoma MPNST Synovial Sarcoma High-risk Sarcoma	Biological: Filgrastim Biological: Filgrastim-SD/01	Phase 1

Detailed Description

Background:

Filgrastim (granulocyte colony-stimulating factor), which is administered by daily subcutaneous injection after cytotoxic chemotherapy, shortens the duration of chemotherapy-induced neutropenia and lowers the risk of infection.
In children treated with dose-intensive chemotherapy, Filgrastim reduces the duration of severe neutropenia and, as a result, has become a standard component of the treatment regimen.
Filgrastim-SD/01 (AMGEN), which is produced by PEGylation of the amino-terminus of Filgrastim, is a sustained duration form of granulocyte colony-stimulating factor.
In phase I and phase II trials in adults, a single dose of Filgrastim-SD/01 appears to be equivalent to daily dosing of Filgrastim in enhancing neutrophil recovery and has a comparable adverse event profile.
Dose-intensive vincristine/cyclophosphamide/doxorubicin (VDoxC) alternating with ifosfamide/etoposide (IE) has become standard therapy for children and adolescents with Ewing's sarcoma and other sarcomas treated at the POB/NCI and other cancer centers within the US.

Objectives:

Compare the tolerance, toxicity, and therapeutic effects of Filgrastim-SD/01 given as a single injection after chemotherapy to daily subcutaneous Filgrastim in patients with newly diagnosed sarcoma receiving multi-agent, dose intensive chemotherapy.
The pharmacokinetics of Filgrastim-SD/01 will also be compared to the pharmacokinetics of Filgrastim.
This trial will also be a platform for performing biological studies of these tumors study neutrophil function and CD34 mobilization, and for detailed cardiac studies.

Eligibility:

Children and young adults (less than or equal to 25 years) with previously untreated high-risk sarcomas (Ewing sarcoma, rhabdomyosarcoma, MPNST, and synovial sarcoma).
No evidence of tumor infiltration of the bone marrow.

Design:

Participants will be randomized (1:1) to receive a single dose of Filgrastim-SD/01 or daily filgrastim as a SQ injection after each cycle of chemotherapy.
Standard 5 drug dose-intensive chemotherapy with vincristine, doxorubicin, cyclophosphamide alternating with ifosfamide and etoposide will be administered.
Surgery or radiation for the primary tumor will occur after cycle 5.
A total of 34 patients (17 patients per treatment arm) will be entered onto the trial.

Study Design

Study Type:

Interventional

Actual Enrollment :

34 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Randomized Trial of Filgrastim-SD/01 vs. Filgrastim in Newly Diagnosed Children and Young Adults With Sarcoma Treated With Dose-Intensive Chemotherapy

Study Start Date :

Mar 3, 2000

Actual Primary Completion Date :

May 20, 2009

Actual Study Completion Date :

May 20, 2009

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 1 single dose of intervention after each cycle of Standard 5 drug dose-intensive chemotherapy	Biological: Filgrastim 5 microgram/kg/dose SC daily starting 24-36 hours after last dose of chemotherapy until post-nadir ANC >=10,000/microliter
Experimental: 2 single dose of interventionafter each cycle of Standard 5 drug dose-intensive chemotherapy	Biological: Filgrastim-SD/01 100 microgram/kg SC 24-36 hours after last dose of chemotherapy (single dose)

Arm

Intervention/Treatment

Experimental: 1

single dose of intervention after each cycle of Standard 5 drug dose-intensive chemotherapy

Biological: Filgrastim

5 microgram/kg/dose SC daily starting 24-36 hours after last dose of chemotherapy until post-nadir ANC >=10,000/microliter

Experimental: 2

single dose of interventionafter each cycle of Standard 5 drug dose-intensive chemotherapy

Biological: Filgrastim-SD/01

100 microgram/kg SC 24-36 hours after last dose of chemotherapy (single dose)

Outcome Measures

Primary Outcome Measures

Tolerance and toxicity [1 year]
PKs [1 year]

Secondary Outcome Measures

Compare neutrophil function []
Compare CD34 positive stem cell mobilization []
Compare days of febrile neutropenia, days on antibiotics, and inpatient days resulting from neutropenia []
Evaluate the role of functional cardiac MRI and serum troponin T levels in detecting early doxorubicin cardiotoxicity []
Assess methods of detecting minimal residual disease []
cDNA microarray analysis of gene expression, development of cell lines and xenotransplantation models, and exploration of apoptotic pathways []

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A to 25 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

INCLUSION CRITERIA:
Newly diagnosed histologically proven:
Ewing's sarcoma family of tumors, including peripheral neuroectodermal tumors;
Alveolar rhabdomyosarcoma;
Stage 3 or 4 embryonal rhabdomyosarcoma;
Malignant peripheral nerve sheath tumor that is unresectable, incompletely resected with bulk residual disease or metastatic;
Synovial cell sarcoma that is unresectable, incompletely resected with bulk residual disease, or metastatic.
Age equal to or less than 25 years at the time of diagnosis.
Normal cardiac function (ejection fraction by MUGA or ECHO that is within the institutional normal range).
Normal serum creatinine for age or creatinine clearance greater than 60 ml/min/1.73m(2).
Normal liver function (SGPT less than 5 times the upper limit of normal and bilirubin less than 2.5 times the upper limit of normal).
Normal hematologic function (absolute neutrophil count equal to or greater than 1500/microL, hemoglobin equal to or greater than 9.0 g/dl and platelet count equal to or greater than 100,000/microL).
Subjects of childbearing or child-fathering potential must be willing to use a medically acceptable form of birth control, which includes abstinence, while being treated on this study.

EXCLUSION CRITERIA:

Previous chemotherapy or radiotherapy.
Pregnant or breast feeding females because the chemotherapy administered on this trial could have a detrimental effect on the developing fetus or newborn.
Histological evidence of tumor infiltration of bone marrow.
Stage 1 or 2 embryonal rhabdomyosarcomas.