Observation and/or Combination Chemotherapy After Surgery or Biopsy in Treating Young Patients With Extracranial Germ Cell Tumors

Last updated: September 16, 2013
Sponsor: Children's Cancer and Leukaemia Group
Overall Status: Trial Status Unknown

Phase

3

Condition

Vaginal Cancer

Germ Cell Tumors

Neoplasms

Treatment

N/A

Clinical Study ID

NCT00274950
CDR0000454553
EUDRACT-2004-002503-33
CCLG-GC-2005-04
EU-20584
  • Ages < 17
  • All Genders

Study Summary

RATIONALE: Sometimes, after surgery, the tumor may not need additional treatment until it progresses. In this case, observation may be sufficient. 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 after surgery may kill any remaining tumor cells.

PURPOSE: This phase III trial is studying how well observation and/or combination chemotherapy works after surgery or biopsy in treating young patients with extracranial germ cell tumors.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS:

  • Histologically* proven extracranial malignant germ cell tumor (GCT), including mature/immature teratoma, with or without elevated alpha-fetoprotein (AFP) or human chorionic gonadotropin (HCG) levels

  • Newly diagnosed disease

  • Patients with relapsed or progressive extracranial malignant GCT allowed if previously treated with carboplatin, etoposide, and bleomycin (JEB) chemotherapy

  • Patients relapsing following JEB are eligible for the study relapse strategy NOTE: *Patients with unequivocally raised AFP/HCG whose risk of biopsy is felt to be high can be diagnosed by clinical grounds, imaging, and markers

  • No intracranial GCTs

PATIENT CHARACTERISTICS:

  • Neutrophil count ≥ 1,000/mm^3

  • Platelet count ≥ 100,000/mm^3

  • Bilirubin ≤ 2 times upper limit of normal (ULN)

  • ALT ≤ 3 times ULN

  • Not pregnant or nursing

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics

  • No prior chemotherapy other than JEB

Study Design

Total Participants: 105
Study Start date:
May 01, 2005
Estimated Completion Date:

Study Description

OBJECTIVES:

  • Stratify and reduce treatment for pediatric patients with extracranial germ cell tumors while maintaining event-free survival.

  • Treat newly diagnosed patients with extracranial germ cell tumors requiring chemotherapy with a carboplatin-based strategy.

  • Develop a common strategy for the treatment of patients with recurrent or progressive extracranial germ cell tumors.

  • Register all cases of mature and immature teratoma.

  • Develop a common strategy for the management of immature and mature teratoma, including follow-up strategies to permit early detection of yolk sac recurrence.

OUTLINE: This is a multicenter study.

Patients who have not had prior biopsy or surgical resection undergo biopsy (if feasible) or surgical resection. Patients with mature or immature teratoma undergo observation. These patients who relapse (i.e., tumor regrowth) may undergo further surgical resection unless tumor markers are significantly elevated. If the tumor markers are significantly elevated, these patients proceed to JEB chemotherapy according to risk group. Patients with all other malignant germ cell tumors are assigned to 1 of 3 treatment groups according to risk.

  • Low-risk group: Patients with normal tumor markers undergo observation. Patients with rising tumor markers only AND no imageable tumor proceed to treatment as in the intermediate-risk group. Patients with rising tumor markers AND/OR imageable tumor are considered to have relapsed and proceed to treatment as in the intermediate- or high-risk group.

  • Intermediate-risk group: Patients receive JEB chemotherapy comprising etoposide IV over 4 hours on days 1-3, carboplatin IV over 1 hour on day 2, and bleomycin IV over 30 minutes on day 3. Treatment repeats every 21 days for 4 courses. Patients with residual tumors after completion of chemotherapy may undergo second-look surgery.

  • High-risk group: Patients receive JEB chemotherapy as in the intermediate-risk group for 6 courses. Patients with residual tumors after completion of chemotherapy may undergo second-look surgery.

  • Relapse therapy: Patients in the intermediate- or high-risk group who relapse after completion of JEB chemotherapy receive vinblastine IV on days 1 and 2, ifosfamide IV over 1 hour on days 1-5, and cisplatin IV on days 1-5. Treatment repeats every 21 days for 6 courses.

PROJECTED ACCRUAL: A total of 105 patients will be accrued for this study.

Connect with a study center

  • Our Lady's Hospital for Sick Children Crumlin

    Dublin, 12
    Ireland

    Site Not Available

  • Birmingham Children's Hospital

    Birmingham, England B4 6NH
    United Kingdom

    Site Not Available

  • Institute of Child Health at University of Bristol

    Bristol, England BS2 8AE
    United Kingdom

    Site Not Available

  • Addenbrooke's Hospital

    Cambridge, England CB2 2QQ
    United Kingdom

    Site Not Available

  • Leeds Cancer Centre at St. James's University Hospital

    Leeds, England LS9 7TF
    United Kingdom

    Site Not Available

  • Leicester Royal Infirmary

    Leicester, England LE1 5WW
    United Kingdom

    Site Not Available

  • Royal Liverpool Children's Hospital, Alder Hey

    Liverpool, England L12 2AP
    United Kingdom

    Site Not Available

  • Great Ormond Street Hospital for Children

    London, England WC1N 3JH
    United Kingdom

    Site Not Available

  • Royal London Hospital

    London, England E1 1BB
    United Kingdom

    Site Not Available

  • Royal Manchester Children's Hospital

    Manchester, England M27 4HA
    United Kingdom

    Site Not Available

  • Sir James Spence Institute of Child Health at Royal Victoria Infirmary

    Newcastle-Upon-Tyne, England NE1 4LP
    United Kingdom

    Site Not Available

  • Queen's Medical Centre

    Nottingham, England NG7 2UH
    United Kingdom

    Site Not Available

  • Children's Hospital - Sheffield

    Sheffield, England S10 2TH
    United Kingdom

    Site Not Available

  • Southampton General Hospital

    Southampton, England SO16 6YD
    United Kingdom

    Site Not Available

  • Royal Marsden - Surrey

    Sutton, England SM2 5PT
    United Kingdom

    Site Not Available

  • Royal Belfast Hospital for Sick Children

    Belfast, Northern Ireland BT12 6BE
    United Kingdom

    Site Not Available

  • Royal Aberdeen Children's Hospital

    Aberdeen, Scotland AB25 2ZG
    United Kingdom

    Site Not Available

  • Royal Hospital for Sick Children

    Edinburgh, Scotland EH9 1LF
    United Kingdom

    Site Not Available

  • Royal Hospital for Sick Children

    Glasgow, Scotland G3 8SJ
    United Kingdom

    Site Not Available

  • Childrens Hospital for Wales

    Cardiff, Wales CF14 4XW
    United Kingdom

    Site Not Available

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