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Status unknownNCT00287950Updated Sep 17, 2013

Combination Chemotherapy, Surgery, and Radiation Therapy in Treating Infants With Neuroblastoma

An interventional study of carboplatin and cisplatin in Neuroblastoma, sponsored by Children's Cancer and Leukaemia Group. Status unknown at 22 sites in 2 countries. Open to participants aged Up to 1 Year. Per ClinicalTrials.gov, last updated 2013-09-17.

Sponsored by Children's Cancer and Leukaemia Group · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2006), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Non-randomized
Ages
Up to 1 Year
Sex
All
01

Study summary

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. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving chemotherapy and radiation therapy after surgery may kill any tumor cells that remain after surgery. Sometimes, the tumor may not need any treatment until it progresses. In this case, observation may be sufficient.

PURPOSE: This clinical trial is studying how well giving combination chemotherapy together with surgery and radiation therapy works in treating infants with neuroblastoma.

Read the detailed description

OBJECTIVES:

  • Register all children \< 12 months of age diagnosed with neuroblastoma.
  • Evaluate possible prognostic factors in these patients with particular reference to the collection of biological material.
  • Correlate outcome with factors other than stage in these patients.
  • Determine criteria to modify treatment for some children with advanced disease without impairing survival.

OUTLINE: This is a nonrandomized, multicenter study. Patients are assigned to 1 of 4 treatment groups according to disease stage.

  • Group 1 (stage 1, 2A, or 2B disease): Patients undergo surgical resection of the tumor. Patients with paraspinal tumors may receive chemotherapy* to shrink the tumor before undergoing surgery. Patients with local recurrence after surgery proceed to treatment as in group 3. Patients with metastatic recurrence after surgery proceed to treatment as in group 4.
  • Group 2 (stage 4S disease): Patients undergo observation only. Patients with hepatomegaly or progressive disease may receive chemotherapy*. Patients who do not respond to chemotherapy may undergo up to 4 courses of radiotherapy.
  • Group 3 (stage 3 disease): Patients receive OPEC chemotherapy comprising vincristine IV and cyclophosphamide IV on day 1, cisplatin IV continuously over 24 hours on day 1, and etoposide IV over 4 hours on day 3 during courses 1, 3, and 5. Patients receive OJEC chemotherapy comprising vincristine IV, cyclophosphamide IV, etoposide IV over 4 hours, and carboplatin IV over 1 hour on day 1 during courses 2, 4, and 6. Courses repeat every 3 weeks with alternating OPEC and OJEC chemotherapy for 6 courses. Patients with residual disease then receive 4 additional courses of alternating OPEC and OJEC chemotherapy. Patients whose tumor becomes resectable after either 6 or 10 courses of chemotherapy undergo surgery. Patients with residual disease after 10 courses of chemotherapy are assessed by regular scans. Patients with disease progression on scans undergo radiotherapy. Patients with ganglioneuroma or total necrosis only with no evidence of neuroblastoma after either 6 or 10 courses of chemotherapy receive no further treatment.
  • Group 4 (stage 4 disease): Patients receive alternating courses of OPEC and OJEC for 6 courses as in group 3. Patients who do not achieve metastatic complete response (CR) receive 4 additional courses of alternating OPEC and OJEC chemotherapy. Patients achieving metastatic CR after either 6 or 10 courses of chemotherapy undergo surgery to remove the tumor. Patients with macroscopic residual disease on resected specimen receive 4 additional courses of alternating OPEC and OJEC chemotherapy and then undergo biopsy. Patients with residual disease on biopsy are assessed by regular scans. Patients with disease progression on scans undergo radiotherapy. Patients with ganglioneuroma or total necrosis only after surgery with or without the 4 additional courses of chemotherapy receive no further treatment.

NOTE: * OJEC chemotherapy with a lower dose of carboplatin

After completion of study treatment, patients are followed periodically.

PROJECTED ACCRUAL: A total of 120 patients will be accrued for this study.

02

Conditions studied

  • Neuroblastoma

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Keywords

  • disseminated neuroblastoma
  • localized resectable neuroblastoma
  • localized unresectable neuroblastoma
  • regional neuroblastoma
  • stage 4S neuroblastoma
03

In context

Neuroblastoma

625 studies on the registry are indexed under Neuroblastoma; 122 are open to participants now.

This study's planned enrollment of 120 is above the median of 32 across 475 interventional studies indexed under Neuroblastoma.

Browse Neuroblastoma studies →

Lead sponsor

Children's Cancer and Leukaemia Group is the lead sponsor of 44 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 1 Year
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed newly diagnosed neuroblastoma

    • Any stage disease
    • No previously treated disease
    • Must be diagnosed before the first birthday
  • Must be able to start treatment before reaching 13 months of age

PATIENT CHARACTERISTICS:

  • Not specified

PRIOR CONCURRENT THERAPY:

  • Not specified
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Masking
None (open label)
Enrollment
120 participants (estimated)

Interventions

  • Drugcarboplatin
  • Drugcisplatin
  • Drugcyclophosphamide
  • Drugetoposide
  • Drugvincristine sulfate
  • Procedureadjuvant therapy
  • Procedureconventional surgery
  • Procedureneoadjuvant therapy
  • Radiationradiation therapy
06

Study locations

22 sites
  • Our Lady's Hospital for Sick Children
    Dublin, 12, Ireland
  • Birmingham Children's Hospital
    Birmingham, England B4 6NH, United Kingdom
  • Institute of Child Health at University of Bristol
    Bristol, England BS2 8AE, United Kingdom
  • Addenbrooke's Hospital at Cambridge University Hospitals NHS Foundation Trust
    Cambridge, England CB2 2QQ, United Kingdom
  • Leeds Cancer Centre at St. James's University Hospital
    Leeds, England LS9 7TF, United Kingdom
  • Leicester Royal Infirmary
    Leicester, England LE1 5WW, United Kingdom
  • Royal Liverpool Children's Hospital, Alder Hey
    Liverpool, England L12 2AP, United Kingdom
  • Royal London Hospital
    London, England E1 1BB, United Kingdom
  • Great Ormond Street Hospital for Children NHS Trust
    London, England WC1N 3JH, United Kingdom
  • Meyerstein Institute of Oncology at University College of London Hospitals
    London, England WIT 3AA, United Kingdom
  • Central Manchester and Manchester Children's University Hospitals NHS Trust
    Manchester, England M27 4HA, United Kingdom
  • Sir James Spence Institute of Child Health
    Newcastle-Upon-Tyne, England NE1 4LP, United Kingdom
  • Queen's Medical Centre
    Nottingham, England NG7 2UH, United Kingdom
  • Oxford Radcliffe Hospital
    Oxford, England 0X3 9DU, United Kingdom
  • Children's Hospital - Sheffield
    Sheffield, England S10 2TH, United Kingdom
  • Southampton General Hospital
    Southampton, England SO16 6YD, United Kingdom
  • Royal Marsden NHS Foundation Trust - Surrey
    Sutton, England SM2 5PT, United Kingdom
  • Royal Belfast Hospital for Sick Children
    Belfast, Northern Ireland BT12 6BE, United Kingdom
  • Royal Aberdeen Children's Hospital
    Aberdeen, Scotland AB25 2ZG, United Kingdom
  • Royal Hospital for Sick Children
    Edinburgh, Scotland EH9 1LF, United Kingdom
  • Royal Hospital for Sick Children
    Glasgow, Scotland G3 8SJ, United Kingdom
  • Childrens Hospital for Wales
    Cardiff, Wales CF14 4XW, United Kingdom
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00287950
Lead sponsor
Children's Cancer and Leukaemia Group
First posted
Feb 7, 2006
Start date
Sep 1992
Last update
Sep 17, 2013

Study contacts

Penelope Brock, MD, PhD
study chair · University College London Hospitals
Mary P. Gerrard, MBChB, FRCP, FRCPCH
Children's Hospital - Sheffield
Andrew David J. Pearson, MD, FRCP, DCh
University of Newcastle Upon-Tyne
S. J. Keith Holmes, DO
St. George's Hospital
Ann Barrett
University of Glasgow
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Dec 2006. You cannot join it, but the record below documents what was studied.

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