NeuroblastomaPhase 1NCT00084422
N2001-03: CEP-701 in Treating Young Patients With Recurrent or Refractory High-Risk Neuroblastoma
A Phase 1 study testing lestaurtinib in people with Neuroblastoma, run by New Approaches to Neuroblastoma Therapy Consortium at 12 sites in 2 countries.
Trial summary
RATIONALE: CEP-701 may stop the growth of tumor cells by blocking the enzymes necessary for their growth. PURPOSE: This phase I trial is studying the side effects and best dose of CEP-701 in treating young patients with recurrent or refractory high-risk neuroblastoma. Read more about this study
- Who is it for?
- Ages 1 day to 30 years
- Conditions the study is for
- Neuroblastoma
- What is being tested?
- lestaurtinib
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 47 participants
- Where
- 12 sitesin 2 countries
- Study dates
- Aug 2003to Feb 2011
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 day to 30 years
- All sexes
- No healthy volunteers
- Child, Adult
DISEASE CHARACTERISTICS:
- Diagnosis of neuroblastoma confirmed by at least 1 of the following:
- Histology
- Demonstrates clumps of tumor cells in the bone marrow with elevated urinary catecholamine metabolites
- Recurrent or resistant/refractory disease
- Neuroblastoma metastatic to the bone marrow with granulocytopenia, anemia, and/or thrombocytopenia allowed
- High-risk disease
- Patients in first response after completion of a prior front-line myeloablative regimen OR who were medically ineligible to receive a front-line myeloablative regimen must meet at least 1 of the following criteria:
- Viable neuroblastoma determined by biopsy of a persistent lesion as seen on CT scan, MRI, or metaiodobenzylguanidine (MIBG) scan
- If lesion was irradiated, biopsy must be performed at least 4 weeks after completion of prior radiotherapy
- Morphologic evidence of tumor in bone marrow
- Second or greater response (without histologic confirmation) allowed
- Meets at least 1 of the following criteria:
- At least 1 unidimensionally measurable lesion on CT scan, MRI, or X-ray
- At least 20 mm by conventional techniques OR at least 10 mm by spiral CT scan
- MIBG scan with positive uptake at a minimum of 1 site
- Bone marrow with tumor cells on routine morphology (not by NSE staining only) of bilateral aspirate and/or biopsy AND/OR at least 5 tumor cells/10^6 mononuclear cells in the bone marrow by immunocytologic analysis of 2 consecutive bone marrows performed at least 1 day but no more than 4 weeks apart
PATIENT CHARACTERISTICS:
Age
- 21 and under at diagnosis
Performance status
- Karnofsky 50-100% (for patients > 16 years of age)
- Lansky 50-100% (for patients ≤ 16 years of age)
Life expectancy
- More than 2 months
Hematopoietic
- See Disease Characteristics
- Absolute neutrophil count ≥ 1,000/mm^3
- Platelet count ≥ 50,000/mm^3 (transfusion independent)
- Hemoglobin ≥ 8.0 g/dL (red blood cell transfusions allowed)
Hepatic
- ALT and AST ≤ 3.0 times upper limit of normal (ULN)
- Total bilirubin ≤ 1.5 times ULN
Renal
- Creatinine ≤ 1.5 times normal OR
- Creatinine clearance or radioisotope glomerular filtration rate ≥ 60 mL/min
Cardiovascular
- Ejection fraction ≥ 50% by echocardiogram or MUGA OR
- Fractional shortening ≥ 28% or above lower limit of normal by echocardiogram
Pulmonary
- Lung function normal
- No dyspnea at rest
- No exercise intolerance
- No supplemental oxygen requirement
Other
- Not pregnant
- Negative pregnancy test
- Fertile patients must use effective contraception
- No uncontrolled infection
- No other concurrent illness that would preclude study treatment
PRIOR CONCURRENT THERAPY:
Biologic therapy
- See Chemotherapy
- At least 2 weeks since prior biologic or non-myelosuppressive therapy and recovered
- More than 7 days since prior growth factors
- No prior allogeneic stem cell transplantation AND no extensive chronic graft-versus-host disease
- No concurrent growth factors except filgrastim (G-CSF) or sargramostim (GM-CSF) administered for neutropenia lasting for more than 7 days or for confirmed or clinical septicemia associated with neutropenia
Chemotherapy
- At least 3 months since prior myeloablative chemotherapy with stem cell transplantation
- At least 2 weeks since prior chemotherapy and recovered
Endocrine therapy
- No concurrent corticosteroid therapy except replacement therapy for adrenal insufficiency or treatment for increased intracranial pressure
Radiotherapy
- See Disease Characteristics
- Recovered from prior radiotherapy
- At least 6 weeks since prior therapeutic-dose MIBG
- At least 6 weeks since prior craniospinal or other radiotherapy involving significant bone marrow (i.e., total pelvis or total abdomen)
- At least 4 weeks since prior radiotherapy to any site biopsied
- At least 2 weeks since prior local palliative radiotherapy (small port)
Surgery
- Not specified
Other
- No prior CEP-701
- No concurrent administration of any of the following CYP3A4 inhibitors:
- Cyclosporine
- Clotrimazole
- Ketoconazole
- Erythromycin
- Clarithromycin
- Troleandomycin
- HIV protease inhibitors
- Nefazodone
- Itraconazole
- Voriconazole
Trial locations and contacts
12 sites in 2 countries.
12 sites in 2 countries
United States11 sites
University of Michigan Comprehensive Cancer Center
Ann Arbor, Michigan, 48109
AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Egleston Campus
Atlanta, Georgia, 30322
Children's Hospital Boston
Boston, Massachusetts, 02115
University of Chicago Comer Children's Hospital
Chicago, Illinois, 60637
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229-3039
Childrens Hospital Los Angeles
Los Angeles, California, 90027-0700
Morgan Stanley Children's Hospital of New York-Presbyterian
New York, New York, 10032
Lucille Salter Packer Children's Hospital, Stanford University
Palo Alto, California, 94305
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, 19104-4318
UCSF Helen Diller Family Comprehensive Cancer Center
San Francisco, California, 94143
Children's Hospital and Regional Medical Center - Seattle
Seattle, Washington, 98105
About this study
Official title: A Phase I Study Of CEP-701 In Patients With Refractory Neuroblastoma (IND # 67,722)
RATIONALE: CEP-701 may stop the growth of tumor cells by blocking the enzymes necessary for their growth.
PURPOSE: This phase I trial is studying the side effects and best dose of CEP-701 in treating young patients with recurrent or refractory high-risk neuroblastoma.
Read the detailed description
OBJECTIVES:
Primary
- Determine the maximum tolerated dose of CEP-701 in pediatric patients with recurrent or refractory high-risk neuroblastoma.
- Determine the dose-limiting toxicity of this drug in these patients.
- Determine the pharmacokinetic behavior of this drug in these patients.
Secondary
- Determine the degree of TrkB tyrosine kinase inhibition activity present in the serum of patients treated with this drug.
- Correlate the degree of TrkB tyrosine kinase inhibition activity in these patients with dose level, pharmacokinetics, and antitumor activity data of this drug.
- Determine the antitumor activity of this drug in these patients.
OUTLINE: This is an open-label, dose-escalation, multicenter study.
Patients receive oral CEP-701 twice daily* on days 1-5, 8-12, 15-19, and 22-26. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
NOTE: *On day 1 of course 1 only, patients receive oral CEP-701 once instead of twice.
Cohorts of 3-6 patients receive escalating doses of CEP-701 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, the dose level is expanded up to 9 patients.
PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.
- Conditions
- Neuroblastoma
- Being tested
- lestaurtinib
- Keywords
- recurrent neuroblastoma
- Medical subject headings
- Neuroblastoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
lestaurtinibDrug
Also called CEP-701
Given orally twice daily x 5 consecutive days followed by a two day rest. 28 days = 1 treatment course. Courses repeated indefinitely without gap provided patient has recovered course from toxicities and no DLTs. Dose level assigned according to the planned dose escalation schedule.
| Study group | Role | What they receive |
|---|---|---|
| Single Group | Experimental | Not described Receives: Drug: lestaurtinib |
What is being measured
The primary outcome is the main question the study is designed to answer.
To determine the maximum tolerated dose (MTD) of CEP-701 given on a twice daily chronic administration schedule (two days on , two days off) to children with high risk relapsed or residual neuroblastoma.
Measured: Within 28 days of treatment at each dose level.
To determine dose limiting toxicities (DLTs) of CEP-701 given on this schedule
Measured: Within first 28 days of therapy.
To characterize the pharmacokinetic (PK) behavior of CEP-701 in children with residual or refractory high-risk neuroblastoma.
Participation in PK studies is voluntary and not a requirement for study entry.
Measured: Days 1,5 and 26 of first course only.
Secondary outcomes (2)
To determine the degree of TrkB tyrosine kinase inhibition activity present in the serum of patients treated with CEP-701, and correlate these findings with dose level, pharmacokinetic and anti-tumor activity data.
Measured: Days 1,5 and 26 of first course only.
To define the antitumor activity of CEP-701, within the confines of a Phase I study.
Measured: Evaluation at end of courses 1, 2, 4 and then every 4 courses until patient goes off therapy.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jun 2004 (estimated)
- Study startAug 2003
- Primary completionSep 2009
- Study completionFeb 2011
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for NeuroblastomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 47 participants (actual)
Sponsor and investigators
- Lead sponsor
- New Approaches to Neuroblastoma Therapy Consortium
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Sponsor
- Investigators
- John M. Maris, MD, Principal investigator, Children's Hospital of PhiladelphiaGarrett M. Brodeur, MD, Study chair, Children's Hospital of Philadelphia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00084422
- Sponsor's protocol ID
- CDR0000363630
- Other IDs
- P01CA081403, NANT-2001-03
- Status last verified
- Apr 2023
- First submitted
- 10 Jun 2004
- Last updated
- 10 Apr 2023
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Minturn JE, Villablanca J, Yanik GA, et al.: Phase I trial of lestaurtinib for children with refractory neuroblastoma (NB): A New Approach to Neuroblastoma Therapy (NANT) Consortium study. [Abstract] J Clin Oncol 28 (Suppl 15): A-9532, 2010.
Maris J, Minturn J, Evans A, et al.: Phase I trial of the orally bioavailable TRK tyrosine kinase inhibitor CEP-701 in refractory neuroblastoma: a New Approaches to Neuroblastoma Therapy (NANT) study. [Abstract] Pediatr Blood Cancer 45 (4 Suppl 1): A-0.129, 416, 2005.
Study at a glance
From the registry record, last updated by the sponsor on 10 Apr 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase I Study Of CEP-701 In Patients With Refractory Neuroblastoma (IND # 67,722)
- ClinicalTrials.gov ID
- NCT00084422
- Acronym / sponsor ID
- CDR0000363630
- Conditions
- Neuroblastoma
- Keywords
- recurrent neuroblastoma
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 47 participants (actual)
- Lead sponsor
- New Approaches to Neuroblastoma Therapy ConsortiumUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Study start
- Aug 2003
- Primary completion
- Sep 2009 (actual)
- Study completion
- Feb 2011 (actual)
- First posted
- 11 Jun 2004 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
RATIONALE: CEP-701 may stop the growth of tumor cells by blocking the enzymes necessary for their growth.
PURPOSE: This phase I trial is studying the side effects and best dose of CEP-701 in treating young patients with recurrent or refractory high-risk neuroblastoma.
Detailed description
OBJECTIVES:
Primary
- Determine the maximum tolerated dose of CEP-701 in pediatric patients with recurrent or refractory high-risk neuroblastoma.
- Determine the dose-limiting toxicity of this drug in these patients.
- Determine the pharmacokinetic behavior of this drug in these patients.
Secondary
- Determine the degree of TrkB tyrosine kinase inhibition activity present in the serum of patients treated with this drug.
- Correlate the degree of TrkB tyrosine kinase inhibition activity in these patients with dose level, pharmacokinetics, and antitumor activity data of this drug.
- Determine the antitumor activity of this drug in these patients.
OUTLINE: This is an open-label, dose-escalation, multicenter study.
Patients receive oral CEP-701 twice daily* on days 1-5, 8-12, 15-19, and 22-26. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
NOTE: *On day 1 of course 1 only, patients receive oral CEP-701 once instead of twice.
Cohorts of 3-6 patients receive escalating doses of CEP-701 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, the dose level is expanded up to 9 patients.
PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Single Group | Experimental | Drug: lestaurtinib |
Who may qualify
- Ages
- 1 day to 30 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| lestaurtinibAlso: CEP-701Given orally twice daily x 5 consecutive days followed by a two day rest. 28 days = 1 treatment course. Courses repeated indefinitely without gap provided patient has recovered course from toxicities and no DLTs. Dose level assigned according to the planned dose escalation schedule. | Drug | Single Group |
Primary outcome
To determine the maximum tolerated dose (MTD) of CEP-701 given on a twice daily chronic administration schedule (two days on , two days off) to children with high risk relapsed or residual neuroblastoma.
Time frame: Within 28 days of treatment at each dose level.
To determine dose limiting toxicities (DLTs) of CEP-701 given on this schedule
Time frame: Within first 28 days of therapy.
To characterize the pharmacokinetic (PK) behavior of CEP-701 in children with residual or refractory high-risk neuroblastoma.
Time frame: Days 1,5 and 26 of first course only.
Participation in PK studies is voluntary and not a requirement for study entry.
2 secondary outcomes
To determine the degree of TrkB tyrosine kinase inhibition activity present in the serum of patients treated with CEP-701, and correlate these findings with dose level, pharmacokinetic and anti-tumor activity data.
Time frame: Days 1,5 and 26 of first course only.
To define the antitumor activity of CEP-701, within the confines of a Phase I study.
Time frame: Evaluation at end of courses 1, 2, 4 and then every 4 courses until patient goes off therapy.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Apr 2023.
- Results publicationMinturn JE, Villablanca J, Yanik GA, et al.: Phase I trial of lestaurtinib for children with refractory neuroblastoma (NB): A New Approach to Neuroblastoma Therapy (NANT) Consortium study. [Abstract] J Clin Oncol 28 (Suppl 15): A-9532, 2010.
- Results publicationMaris J, Minturn J, Evans A, et al.: Phase I trial of the orally bioavailable TRK tyrosine kinase inhibitor CEP-701 in refractory neuroblastoma: a New Approaches to Neuroblastoma Therapy (NANT) study. [Abstract] Pediatr Blood Cancer 45 (4 Suppl 1): A-0.129, 416, 2005.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John M. Maris, MD principal investigator
Children's Hospital of Philadelphia
Garrett M. Brodeur, MD study chair
Children's Hospital of Philadelphia
12 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing lestaurtinib in people with Neuroblastoma, run by New Approaches to Neuroblastoma Therapy Consortium at 12 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in United States, Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To determine the maximum tolerated dose (MTD) of CEP-701 given on a twice daily chronic administration schedule (two days on , two days off) to children with high risk relapsed or residual neuroblastoma. (time frame: Within 28 days of treatment at each dose level.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00084422, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2023.