Endometrial Cancer Clinical Trial
Official title:
A Randomized Study of Doxorubicin Plus Cisplatin Versus Doxorubicin Plus Cisplatin Plus 3-Hour Paclitaxel With G-CSF Support in Patients With Primary Stage III & IV or Recurrent Endometrial Carcinoma
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing
so they stop growing or die. Combining more than one drug may kill more tumor cells.
PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy
consisting of doxorubicin and cisplatin with or without paclitaxel and G-CSF in treating
patients who have stage III, stage IV, or recurrent endometrial cancer.
OBJECTIVES:
- Determine whether the addition of paclitaxel, using filgrastim (G-CSF) support, to
standard doxorubicin/cisplatin chemotherapy produces improvement in the frequency of
objective response, progression-free survival, or overall survival in patients with
stage III, stage IV, or recurrent endometrial carcinoma.
- Compare the toxicities of these two regimens in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2
treatment arms.
- Arm I: Patients receive doxorubicin IV over 15-30 minutes, followed immediately by
cisplatin IV over 1 hour.
- Arm II: Patients receive doxorubicin and cisplatin as in arm I on day 1. On day 2,
patients receive paclitaxel IV over 3 hours. Patients also receive filgrastim (G-CSF)
subcutaneously beginning on day 3 and continuing for at least 10 days.
Courses are repeated every 21 days. Treatment continues for up to 7 courses in the absence
of disease progression or unacceptable toxicity.
Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then
annually thereafter.
PROJECTED ACCRUAL: A total of 240 patients (120 per arm) will be accrued for this study
within 21 months.
;
Allocation: Randomized, Primary Purpose: Treatment
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