Fallopian Tube Cancer Clinical Trial
Official title:
Randomized Phase III Trial of Conventional Paclitaxel and Carboplatin Versus Dose Dense Weekly Paclitaxel and Carboplatin in Patients With Newly Diagnosed Stage II-IV Mullerian Carcinoma
The purpose of the study is to compare progression-free survival of conventional paclitaxel and carboplatin vs weekly paclitaxel and carboplatin in patients with newly diagnosed stage II-IV ovarian epithelial, primary peritoneal, or fallopian tube cancer.
This is a randomized, multicenter study. Patients are stratified according to residual
disease 1 cm or less vs more than 1cm, stage II vs III vs IV, and histology (clear cell or
mucinous vs. serous or others). Patients are randomized to one of two treatment arms.
Arm I: Patients receive paclitaxel IV over 3 hours and carboplatin IV over 60 minutes on day
1 for 6-9 cycles.
Arm II: Patients receive paclitaxel IV over 1 hour days 1, 8, and 15 and carboplatin IV over
60 minutes on day 1 for 6-9 cycles.
In both arms, cycles repeat 6 cycles every 21 days in the absence of disease progression or
unacceptable toxicity. Additional 3 cycles are given if clinical partial or complete response
after 6 cycles.
PROJECTED ACCRUAL: A total 600 patients (300 per treatment arm) will be accrued for this
study within 3 years. Assuming median progression-free survivals of 16 months and 21 months
and a recruitment period of 3 years this can be achieved by recruiting 600 patients designed
to have 80 % detect to a difference between the two arms at the two-sided 5% level of
statistical significance.
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