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Randomized Phase II/III Study of Taxol/Paclitaxel-BEP Versus BEP in Patients With Intermediate Prognosis Germ Cell Cancer (NCT00003643)

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which regimen of combination chemotherapy may be more effective for germ cell cancer. PURPOSE: This randomized phase II/III trial is studying two different regimens of combination chemotherapy and comparing how well they work in treating men with germ cell cancer.
  • Biological: bleomycin sulfate
    • Biological: filgrastim
      • Drug: cisplatin
        • Drug: etoposide
          • Drug: paclitaxel
            Ages eligible for Study
            16 Years to 50 Years
            Genders eligible for Study
            Accepts Healthy Volunteers

            Phase II

            - Compare the complete response rates in men with intermediate prognosis germ cell cancer treated with bleomycin, cisplatin, and etoposide (BEP) vs bleomycin, cisplatin, etoposide, and paclitaxel (T-BEP).

            - Define the toxicity profile of T-BEP in these patients.

            Phase III

            - Compare the disease-free survival of patients treated with these regimens.

            - Compare the complete response rates and overall survival of patients treated with these regimens.

            - Compare symptoms and aspects of quality of life at baseline and after treatment in patients treated with these regimens.

            - Compare the acute and intermediate (1-2 years) side effects of these regimens in these patients.

            OUTLINE: This is a randomized, multicenter study. Patients are stratified according to histology (seminoma vs non-seminoma) and hospital. Patients are randomized to 1 of 2 treatment arms.

            - Arm I: Patients receive cisplatin IV and etoposide IV on days 1-5 and bleomycin IV on days 1, 8, and 15.

            - Arm II: Patients receive cisplatin, etoposide, and bleomycin as in arm I and paclitaxel IV over 3 hours on day 1. Patients also receive filgrastim (G-CSF) subcutaneously on days 6-15.

            In both arms, treatment repeats every 3 weeks for a total of 4 courses in the absence of disease progression or unacceptable toxicity.

            Quality of life is assessed before treatment randomization and at 1 and 2 years after randomization.

            Patients are followed monthly for 1 year, every 2 months for 1 year, every 3 months for 1 year, every 6 months for 1 year, and then annually thereafter.

            PROJECTED ACCRUAL: A total of 84-164 patients (42-82 per treatment arm) will be accrued for the phase II study. A total of 498 patients (249 per treatment arm) will be accrued for the phase III study. Accrual will be completed within 4 years.

            69 locations

            Ⅱ, Ⅲ
            30 September, 1998
            04 March, 2012
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