RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of aminopterin in treating patients who have refractory or recurrent endometrial cancer.
OBJECTIVES: I. Estimate the antitumor activity of aminopterin in patients with persistent, recurrent, or refractory endometrial carcinoma who have failed prior first line cytotoxic chemotherapy. II. Determine the quantitative and qualitative toxic effects of aminopterin in this patient population. III. Determine the overall patient survival and time to progression of these patients. IV. Assess the pharmacokinetic profile of these patients. OUTLINE: Patients receive oral aminopterin every 12 hours twice weekly. Treatment continues for up to 15 months in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months until death. PROJECTED ACCRUAL: A total of 15-25 patients will be accrued for this study.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Division of Gynecologic Oncology
St Louis, Missouri, United States
East Carolina University School of Medicine
Greenville, North Carolina, United States
Gynecologic Oncologists of NE Ohio
Akron, Ohio, United States
Simmons Cancer Center - Dallas
Dallas, Texas, United States
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Texas Oncology, P.A.
Dallas, Texas, United States
University of Wisconsin Comprehensive Cancer Center
Madison, Wisconsin, United States