The purpose of this study is to treat advanced or recurrent endometrial cancer, paclitaxel-containing regimen is the preferred chemotherapeutic regimen which is selected by most physicians. Docetaxel may have similar efficacy and more favorable treatment related toxicity profile as tested in epithelial ovarian cancer trials. Therefore, the investigators aimed to evaluate the efficacy and safety of docetaxel plus cisplatin in patients with advanced or recurrent endometrial cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
59
Asan Medical Center
Seoul, South Korea
RECRUITINGResponse rate
Time frame: 3 months after completion of study treatment
Progression-free survival
Time frame: 2 years after completion of study treatment
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Time frame: Before each chemotherapy, an expected average of 3 weeks
Quality of life
Time frame: 3 months after completion of study treatment
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