Neuroblastoma Clinical Trial
Official title:
Randomized Study of Radiotherapy in Patients With Stage 2B/3 (INSS) Neuroblastoma in Children Over 1 Year of Age
RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor
cells, either by killing the cells or by stopping them from dividing. Giving more than one
drug (combination chemotherapy) may kill more tumor cells. Giving combination chemotherapy
before surgery may make the tumor smaller and reduce the amount of normal tissue that needs
to be removed. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving
radiation therapy after surgery may kill any tumor cells that remain. It is not yet know
whether combination chemotherapy followed by surgery alone is more effective than
combination chemotherapy followed by surgery and radiation therapy in treating
neuroblastoma.
PURPOSE: This randomized phase III trial is studying combination chemotherapy followed by
surgery to see how well it works compared to combination chemotherapy followed by surgery
and radiation therapy in treating young patients with stage II or stage III neuroblastoma.
OBJECTIVES:
- Compare the local control and event-free and overall survival of young patients with
stage IIB and III neuroblastoma treated with neoadjuvant combination chemotherapy
followed by surgery with vs without radiotherapy.
- Determine the toxic effects of these regimen in these patients.
OUTLINE: This is a multicenter, randomized study.
- Induction combination chemotherapy: Patients receive vincristine IV and
cyclophosphamide IV on day 1. Patients also receive cisplatin IV continuously over 24
hours on day 1 and etoposide IV over 4 hours on day 2 during courses 1, 3, and 5 and
carboplatin IV over 1 hour and etoposide IV over 4 hours on day 1 during courses 2 and
4. Treatment repeats every 21 days for 5 courses in the absence of disease progression
or unacceptable toxicity. Patients then proceed to surgery unless complete resection
was done during initial staging and complete response was maintained.
- Surgery: Patients undergo biopsy or surgical resection of the tumor 2-3 weeks after
completion of induction combination chemotherapy.
- Post-surgical treatment: Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive two additional courses of combination chemotherapy
comprising vincristine, cisplatin, etoposide, and cyclophosphamide in course 6 and
vincristine, carboplatin, etoposide, and cyclophosphamide in course 7.
- Arm II: Patients undergo radiotherapy 2-4 weeks after surgery. Beginning 3 weeks
after completion of radiotherapy, patients receive chemotherapy as in arm I After
completion of study treatment, patients are evaluated periodically.
PROJECTED ACCRUAL: A total of 150 patients will be accrued for this study.
;
Allocation: Randomized, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00492167 -
Beta-Glucan and Monoclonal Antibody 3F8 in Treating Patients With Metastatic Neuroblastoma
|
Phase 1 | |
Completed |
NCT04474678 -
Quality Improvement Project - "My Logbook! - I Know my Way Around!"; ("Mein Logbuch - Ich Kenne Mich Aus!")
|
N/A | |
Terminated |
NCT00801931 -
Double Cord Blood Transplant for Patients With Malignant and Non-malignant Disorders
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT03107988 -
NANT 2015-02: A Phase 1 Study of Lorlatinib (PF-06463922)
|
Phase 1 | |
Recruiting |
NCT04253015 -
A Post-Authorisation Safety Study Patient Registry of Patients With Neuroblastoma Being Treated With Dinutuximab Beta
|
||
Terminated |
NCT00788125 -
Dasatinib, Ifosfamide, Carboplatin, and Etoposide in Treating Young Patients With Metastatic or Recurrent Malignant Solid Tumors
|
Phase 1/Phase 2 | |
Completed |
NCT03273712 -
Dosimetry-Guided, Peptide Receptor Radiotherapy (PRRT) With 90Y-DOTA- tyr3-Octreotide (90Y-DOTATOC)
|
Phase 2 | |
Recruiting |
NCT02933333 -
G-CSF Alone or Combination With GM-CSF on Prevention and Treatment of Infection in Children With Malignant Tumor
|
Phase 4 | |
Recruiting |
NCT00588068 -
Molecular Characterization of Neuroblastic Tumor: Correlation With Clinical Outcome
|
||
Recruiting |
NCT04301843 -
Eflornithine (DFMO) and Etoposide for Relapsed/Refractory Neuroblastoma
|
Phase 2 | |
Completed |
NCT00026780 -
Eligibility Screening for a NCI Pediatric Oncology Branch Research Study
|
||
Recruiting |
NCT04040088 -
An Investigational Scan (68Ga-DOTATATE PET/CT) in Diagnosing Pediatric Metastatic Neuroendocrine Tumors
|
Early Phase 1 | |
Recruiting |
NCT06057948 -
A Study of a Vaccine in Combination With Beta-glucan in People With Neuroblastoma
|
Phase 2 | |
Not yet recruiting |
NCT06335745 -
PediCARE Health Equity Intervention in High-Risk Neuroblastoma
|
N/A | |
Recruiting |
NCT02559778 -
Pediatric Precision Laboratory Advanced Neuroblastoma Therapy
|
Phase 2 | |
Completed |
NCT02441062 -
Impact of Ga-68 DOTATOC PET-CT Imaging in Management of Neuroendocrine Tumors
|
Phase 2 | |
Active, not recruiting |
NCT02245997 -
Local Control With Reduced-dose Radiotherapy for High-Risk Neuroblastoma
|
N/A | |
Not yet recruiting |
NCT01156350 -
Haplo-identical Hematopoietic Stem Cell Transplantation Following Reduced-intensity Conditioning in Children With Neuroblastoma
|
Phase 2 | |
Active, not recruiting |
NCT01192555 -
Allogeneic Tumor Cell Vaccination With Oral Metronomic Cytoxan in Patients With High-Risk Neuroblastoma
|
Phase 1/Phase 2 | |
Completed |
NCT01222780 -
To Evaluate the Safety, Activity and Pharmacokinetics of Marqibo in Children and Adolescents With Refractory Cancer
|
Phase 1 |