Clinical Trials Directory

Trials / Completed

CompletedNCT00453232

Combination Chemotherapy and Pegfilgrastim in Treating Men With Metastatic Germ Cell Tumors

Accelerated BEP Chemotherapy for Intermediate and High Risk Metastatic Germ Cell Tumor

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Cambridge University Hospitals NHS Foundation Trust · Academic / Other
Sex
Male
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as bleomycin, etoposide, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Colony-stimulating factors, such as pegfilgrastim, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Giving combination chemotherapy together with pegfilgrastim may kill more tumor cells. PURPOSE: This phase II trial is studying the side effects and how well giving combination chemotherapy together with pegfilgrastim works in treating men with metastatic germ cell tumors.

Detailed description

OBJECTIVES: Primary * Determine the feasibility of accelerated treatment comprising bleomycin, etoposide, cisplatin, and pegfilgrastim in men with metastatic germ cell tumors. * Determine the toxicity of this regimen (particularly with respect to renal, pulmonary, and neurological function) in these patients. Secondary * Determine the response rate in patients treated with this regimen. * Determine the progression-free survival of patients treated with this regimen. OUTLINE: This is a non-randomized, pilot study. Patients receive etoposide IV on days 1-3, cisplatin IV on days 1 and 2, and bleomycin IV over 2 hours on days 2, 6, and 10. Patients also receive pegfilgrastim subcutaneously on day 4. Treatment repeats every 14 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed periodically for 2 years. PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
BIOLOGICALbleomycin sulfate
BIOLOGICALpegfilgrastim
DRUGcisplatin
DRUGetoposide

Timeline

Start date
2004-08-01
Primary completion
2008-12-01
Completion
2009-01-01
First posted
2007-03-28
Last updated
2013-08-07

Locations

7 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00453232. Inclusion in this directory is not an endorsement.