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Etoposide, Carboplatin, and Bleomycin in Treating Young Patients Undergoing Surgery For Malignant Germ Cell Tumors

Active, not recruiting
04/01/1989 to Present
100
N/A
Interventional

Conditions

  • Brain and Central Nervous System Tumors
  • Childhood Germ Cell Tumor
  • Extragonadal Germ Cell Tumor
  • Ovarian cancer

Eligibility

15 and younger
No
DISEASE CHARACTERISTICS:
- Histologically proven malignant germ cell tumors at all stages
- Testicular tumors
- Stage I - Confined to testes
- Stage II - Confined to testes and retroperitoneal/abdominal lymph nodes
- Stage III - Supradiaphragmatic nodal disease (mediastinal and/or
supraclavicular)
- Stage IV - Extralymphatic spread (liver, lung, bone, brain, skin, etc.)
- Ovarian, uterine, vaginal, and sacrococcygeal tumors
- Stage I - Confined to ovary/uterus/vagina/pre- and postsacral area
- Stage II - Spread limited to the pelvis
- Stage III - Spread limited to the abdomen (excluding liver)
- Stage IV - Spread to liver or beyond the abdominal cavity
- Abdominal, retroperitoneal, and thoracic primary tumors
- Stage I - Confined to site of origin and resectable
- Stage II - Local spread
- Stage III - Extensive spread confined to one side of the diaphragm
(excluding the liver)
- Stage IV - Tumor spread to the liver, to both sides of the diaphragm,
and/or to bones, bone marrow, brain, etc.
- Intracranial germ cell tumor cases allowed even if an alternative protocol is
being followed
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- No prior chemotherapy

Purpose

OBJECTIVES:

- Determine the toxic effects of etoposide, carboplatin, and bleomycin in young patients
with malignant germ cell tumors.

OUTLINE: Patients are assigned to one of two treatment arms based on their tumor type
(testicular vs ovarian, uterine, vaginal, sacrococcygeal, retroperitoneal, or thoracic).

- Group 1 (testicular tumors): Patients undergo radical orchiectomy. Patients with stage
I tumors and alpha-fetoprotein (AFP) decreasing at the expected rate receive no further
treatment unless there is a subsequent rise in the AFP or a clinical recurrence.
Patients with stage II-IV tumors receive etoposide IV over 1 hour on days 1-3,
carboplatin IV over 1 hour on day 2, and bleomycin IV over 15 minutes on day 3.
Treatment repeats every 21- 28 days for at least 4 courses in the absence of disease
progression or unacceptable toxicity. Residual teratoma may be removed, if indicated,
after completion of chemotherapy.

- Group 2 (ovarian, uterine, vaginal, sacrococcygeal, retroperitoneal, or thoracic germ
cell tumors): Patients undergo surgical removal or biopsy of the tumor. Patients then
receive etoposide, carboplatin, and bleomycin as above. Patients may then undergo
further surgery at the discretion of the principal investigator.

After completion of study treatment, patients are followed periodically.

PROJECTED ACCRUAL: A total of 100 patients will be accrued for this study.

Interventions

  • Biological: bleomycin sulfate
  • Drug: carboplatin
  • Drug: etoposide
  • Procedure: conventional surgery

Officials

  • A. Oakhill, MD
    Study Chair, Bristol Royal Hospital for Children
  • Michael Sokal
    Nottingham City Hospital NHS Trust
  • P. Gornall, MD
    Birmingham Children's Hospital

Locations

  • Childrens Hospital for Wales
    Cardiff, Wales, CF14 4XW, United Kingdom
    Active, not recruiting
  • Royal Hospital for Sick Children
    Glasgow, Scotland, G3 8SJ, United Kingdom
    Active, not recruiting
  • Royal Hospital for Sick Children
    Edinburgh, Scotland, EH9 1LF, United Kingdom
    Active, not recruiting
  • Royal Aberdeen Children's Hospital
    Aberdeen, Scotland, AB25 2ZG, United Kingdom
    Active, not recruiting
  • Royal Belfast Hospital for Sick Children
    Belfast, Northern Ireland, BT12 6BE, United Kingdom
    Active, not recruiting
  • Royal Marsden NHS Foundation Trust - Surrey
    Sutton, England, SM2 5PT, United Kingdom
    Active, not recruiting
  • Southampton General Hospital
    Southampton, England, SO16 6YD, United Kingdom
    Active, not recruiting
  • Children's Hospital - Sheffield
    Sheffield, England, S10 2TH, United Kingdom
    Active, not recruiting
  • Oxford Radcliffe Hospital
    Oxford, England, 0X3 9DU, United Kingdom
    Active, not recruiting
  • Queen's Medical Centre
    Nottingham, England, NG7 2UH, United Kingdom
    Active, not recruiting
  • Sir James Spence Institute of Child Health
    Newcastle-Upon-Tyne, England, NE1 4LP, United Kingdom
    Active, not recruiting
  • Central Manchester and Manchester Children's University Hospitals NHS Trust
    Manchester, England, M27 4HA, United Kingdom
    Active, not recruiting

Sponsors

  • Children's Cancer and Leukaemia Group
    Lead Sponsor
  • United States: Federal Government

Links

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