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Study of Fixed vs. Flexible Filgrastim to Accelerate Bone Marrow Recovery After Chemotherapy in Children With Cancer

Prospective and Randomized Study of Fixed Versus Flexible Prophylactic Administration of Granulocyte Colony-Stimulating Factor (G-CSF) in Children With Cancer

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01987596
Enrollment
23
Registered
2013-11-19
Start date
2013-08-31
Completion date
2018-06-30
Last updated
2020-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Choroid Plexus Tumor, Childhood Medulloblastoma, Childhood Pineoblastoma, Childhood Soft Tissue Sarcoma, Childhood Supratentorial Primitive Neuroectodermal Tumor, Neuroblastoma, Osteosarcoma, Recurrent/Refractory Childhood Hodgkin Lymphoma, Retinoblastoma, Unspecified Childhood Solid Tumor, Protocol Specific, Wilms Tumor and Other Childhood Kidney Tumors

Brief summary

This randomized phase III trial studies flexible administration of filgrastim after combination chemotherapy to see how well it works compared to fixed administration of filgrastim in decreasing side effects of chemotherapy in younger patients with cancer. Cancer chemotherapy frequently results in neutropenia (low blood counts) when patients are susceptible to severe infections. A medicine called G-CSF (filgrastim) stimulates bone marrow and daily filgrastim shots are commonly used to shorten neutropenic periods and decrease infections after chemotherapy. Since filgrastim is customarily used on a fixed schedule starting early after chemotherapy and there are data that early doses may not be needed, this study tests new flexible schedule of filgrastim to optimize its use by reducing the number of painful shots, cost of treatment, and filgrastim side effects in children with cancer receiving chemotherapy.

Detailed description

PRIMARY OBJECTIVES: I. To compare the effect of flexible vs. fixed administration of G-CSF (filgrastim) on the parameters of hematological recovery including duration of absolute neutrophil count (ANC) \< 500/uL; time to ANC recovery \>= 1,000/uL and time to platelet recovery \>= 75,000/uL in children receiving myelotoxic chemotherapy. SECONDARY OBJECTIVES: I. To compare the effect of flexible vs. fixed administration of G-CSF on the incidence of febrile neutropenia and number of hospital days on antibiotics following myelotoxic chemotherapy. II. To evaluate the number of days of platelet transfusion events after chemotherapy cycles with flexible vs. fixed administration of G-CSF. III. To evaluate on the incidence and duration of G-CSF-related side effects including extremities/back pain and headaches after chemotherapy courses followed by flexible vs. fixed administration of G-CSF. IV. To evaluate the peripheral blood progenitor responses and subsets of progenitor cells (cluster of differentiation \[CD\]34/41/61/117/10/19/11b/33) to chemotherapy followed by flexible vs. fixed administration of G-CSF. OUTLINE: CHEMOTHERAPY: Depending on their diagnosis patients are assigned to 1 of 3 chemotherapy regimens. ICE: Patients receive etoposide intravenously (IV) over 1 hour on days 1-3, ifosfamide IV over 3 hours on days 1-3, and carboplatin IV over 1 hour on day 4. Patients with recurrent Hodgkin lymphoma receive etoposide and ifosfamide on days 1-3 and carboplatin on day 3. ICT: Patients receive topotecan hydrochloride IV over 30 minutes on days 1-3, and ifosfamide and carboplatin as in ICE. OPEC: Patients receive vincristine sulfate on days 1, 8, and 15; etoposide IV over 1 hour on days 1-3; cyclophosphamide IV over 1 hour on days 1-2; and cisplatin IV over 6 hours on day 4. For all chemotherapy regimens, treatment repeats every 21 days for 2 courses. Patients are then randomized to 1 of 2 treatment arms. ARM I (fixed filgrastim): Patients receive filgrastim subcutaneously (SC) once daily (QD) started at 24 hours after completion of chemotherapy and stopped when ANC reaches at least 1,000/uL post nadir. ARM II (flexible filgrastim): Patients receive filgrastim SC QD started on the first day after chemotherapy when ANC falls below 1,000/uL and stopped when ANC reaches at least 1,000/uL post nadir. After completion of the first filgrastim treatment, patients cross-over to the other filgrastim arm and repeat the same course of chemotherapy as before. After completion of the second filgrastim treatment, chemotherapy treatment may continue for up to 5 (OPEC) or 6 (ICE, ICT) courses in the absence of disease progression or unacceptable toxicity.

Interventions

BIOLOGICALfilgrastim

Given SC once daily starting on day 1 after chemotherapy in Arm I (fixed) and on any day when ANC drops below 1000/mcl in Arm II (flexible)

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Children's Hospital of Michigan
CollaboratorOTHER
Barbara Ann Karmanos Cancer Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* Subjects must have or have had at initial diagnosis, histologic proof of their malignancy; young children with primary embryonal brain tumor treated according to Head Start protocol are eligible; subjects with bone marrow involvement are NOT eligible for study * Patients will receive repeated cycles of identical chemotherapy that will likely result in grades III-IV hematological toxicity; patients will be treated outside of Children's Oncology Group (COG) protocols with specific requirements for schedule of G-CSF administration; the following categories of patients treated at Children's Hospital of Michigan are eligible for this study: * Patients with brain tumors treated according to Head Start II protocol with vincristine, etoposide, cyclophosphamide, and cisplatin (OPEC) chemotherapy; * Patients with recurrent Hodgkin lymphoma treated with ICE (ifosfamide, carboplatin, etoposide) chemotherapy; * Patients with recurrent solid tumors including sarcomas, Wilms' tumor, neuroblastomas, or brain tumors treated with high dose ICE or ICT (ifosfamide, carboplatin, topotecan) chemotherapy * Patients with UH Wilms' tumor treated with CE (cyclophosphamide, etoposide); patients with neuroblastoma treated with CE (carboplatin, etoposide); * Patients with soft tissue sarcomas treated with IA (ifosfamide, doxorubicin); * Patients with osteosarcoma treated with high dose ifosfamide * Subjects must have fully recovered from the toxic effects of any prior therapy; at least 3 weeks should have elapsed since the last dose of chemotherapy (6 weeks in the case of nitrosourea containing therapy); subjects must have recovered from previous colony-stimulating factor therapy and have been off colony-stimulating factors (G-CSF, granulocyte macrophage colony-stimulating factor \[GM-CSF\], interleukin \[IL\]-11) for more than 10 days and off erythropoietin for 30 days * ANC \> 1000/uL * Platelet count \> 100,000/uL * Creatinine clearance or glomerular filtration rate (GFR) which is greater than or equal to 70 ml/min/1.73 m\^2 * Bilirubin less than 1.5 x normal limit (NL) * Serum glutamic oxaloacetic transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) less than 2.5 x NL for age * Subjects should have a normal ejection fraction (per institutional limits), no evidence of cardiac arrhythmias requiring therapy, and a fractional shortening of \> 28% * All subjects must have a life expectancy of 12 weeks or more * Diagnostic categories * Sarcoma (soft tissue and bone) * Kidney tumors * Brain tumors * Other solid tumors (gonadal and germ cell tumors, retinoblastoma, neuroblastoma, and miscellaneous tumors) * Hodgkin lymphoma * Performance status must be \> 60 from Lansky (age 1 to 16) or Karnofsky (age \> 16)

Exclusion criteria

* Subjects with any of the following will NOT be eligible for study: * Bone marrow involvement * Active myelogenous leukemia, or history of myelogenous leukemia * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Days to ANC Greater Than or Equal to 1,000/uL From the Start of ChemotherapyFrom the start of the course until the first date the ANC reaches >= 1,000/uL post nadir, assessed up to 1 yearTime in days until absolute neutrophil count (ANC) recovery to greater than or equal to 1,000/uL from the start of chemotherapy

Secondary

MeasureTime frameDescription
Cumulative GCSF Doseup until engraftmentCumulative GCSF dose - number of GCSF injections until ANC recovery greater than or equal to 1,000/uL from the start of chemotherapy
Days to First G-CSF Dosetime to ANC 1000Time (in days) to first G-CSF dose
Incidence of Febrile NeutropeniaUp to 1 yearoccurrence of febrile neutropenia

Countries

United States

Participant flow

Participants by arm

ArmCount
Arm I (Fixed Flexible Filgrastim Schedule)
Period 1 Fixed: Patients receive filgrastim SC QD once daily started at 24 hours after completion of chemotherapy and stopped when ANC reaches at least 1,000/uL post nadir. Period 2 Flexible: Patients receive filgrastim:SC once starting on day 1 after chemotherapy in Arm I (fixed) and on any day when ANC drops below 1000/mcl in Arm II (flexible)
11
Arm II (Flexible Fixed Filgrastim Schedule)
Period 1 Flexible: Patients receive filgrastim SC QD started on the first day after chemotherapy and on any day when ANC falls below 1,000/uL and stopped when ANC reaches at least 1,000/uL post nadir. Period 2 Fixed: Patients receive filgrastim: given SC once daily starting on day 1 after chemotherapy in and daily thereafter until ANC reaches at least 1,000/uL post nadir.
10
Total21

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyPhysician Decision10
Overall StudyProgressive Disease; missing all period01

Baseline characteristics

CharacteristicArm I (Fixed Flexible Filgrastim Schedule)TotalArm II (Flexible Fixed Filgrastim Schedule)
Age, Continuous16 years14 years11 years
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants1 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
10 Participants20 Participants10 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Black or African American
4 Participants8 Participants4 Participants
Race (NIH/OMB)
More than one race
3 Participants3 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
4 Participants9 Participants5 Participants
Region of Enrollment
United States
11 participants21 participants10 participants
Sex: Female, Male
Female
2 Participants7 Participants5 Participants
Sex: Female, Male
Male
9 Participants14 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 210 / 21
other
Total, other adverse events
4 / 211 / 21
serious
Total, serious adverse events
0 / 210 / 21

Outcome results

Primary

Days to ANC Greater Than or Equal to 1,000/uL From the Start of Chemotherapy

Time in days until absolute neutrophil count (ANC) recovery to greater than or equal to 1,000/uL from the start of chemotherapy

Time frame: From the start of the course until the first date the ANC reaches >= 1,000/uL post nadir, assessed up to 1 year

ArmMeasureValue (MEAN)
FixedDays to ANC Greater Than or Equal to 1,000/uL From the Start of Chemotherapy16.0 days
FlexibleDays to ANC Greater Than or Equal to 1,000/uL From the Start of Chemotherapy16.7 days
Secondary

Cumulative GCSF Dose

Cumulative GCSF dose - number of GCSF injections until ANC recovery greater than or equal to 1,000/uL from the start of chemotherapy

Time frame: up until engraftment

Population: Patients who had data for period 2

ArmMeasureValue (MEAN)
FixedCumulative GCSF Dose10.5 Doses
FlexibleCumulative GCSF Dose6.7 Doses
Comparison: two-period crossover design analysisp-value: <0.0001ANOVA
Secondary

Days to First G-CSF Dose

Time (in days) to first G-CSF dose

Time frame: time to ANC 1000

Population: All participants with period 2 data

ArmMeasureValue (MEAN)
FixedDays to First G-CSF Dose5.1 days
FlexibleDays to First G-CSF Dose9.5 days
Comparison: 2 treatment, 2 periiod cross-over analysisp-value: <0.0001ANOVA
Secondary

Incidence of Febrile Neutropenia

occurrence of febrile neutropenia

Time frame: Up to 1 year

Population: Each patient server as his/her own control

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
FixedIncidence of Febrile NeutropeniaYes5 Participants
FixedIncidence of Febrile NeutropeniaNo16 Participants
FlexibleIncidence of Febrile NeutropeniaYes6 Participants
FlexibleIncidence of Febrile NeutropeniaNo15 Participants
p-value: 1McNemar

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026