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Combination Chemotherapy Compared With Hormone Therapy in Treating Patients With Recurrent, Stage III, or Stage IV Endometrial Cancer

Phase 3
Terminated
Conditions
Endometrial Cancer
Registration Number
NCT00016341
Lead Sponsor
Gynecologic Oncology Group
Brief Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Estrogen can stimulate the growth of tumor cells. Hormone therapy using tamoxifen and megestrol may fight endometrial cancer by blocking the absorption of estrogen. It is not yet known whether chemotherapy is more effective than hormone therapy in treating endometrial cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy with that of hormone therapy in treating patients who have recurrent, stage III, or stage IV endometrial cancer.

Detailed Description

OBJECTIVES:

* Compare the progression-free survival and response of patients with stage III or IV or recurrent endometrial cancer treated with doxorubicin, cisplatin, paclitaxel, and filgrastim (G-CSF) vs tamoxifen and megestrol.

* Compare the survival of patients treated with these regimens.

* Determine if progesterone receptor status provides information on whether patients are more likely to benefit from chemotherapy.

* Compare the toxicity profiles of these treatment regimens in these patients.

* Compare the quality of life of patients treated with these regimens.

OUTLINE: This is a randomized, cross-over, multicenter study. Patients are stratified according to progesterone receptor status (negative vs positive). Patients are randomized to 1 of 2 treatment arms.

* Arm I:Patients receive chemotherapy comprising doxorubicin IV over 15-30 minutes followed by cisplatin IV over 1 hour on day 1; paclitaxel IV over 3 hours on day 2; and filgrastim (G-CSF) subcutaneously beginning on day 3 and continuing for 10 days. Chemotherapy repeats every 21 days for up to 7 courses in the absence of disease progression or unacceptable toxicity.

* At time of disease progression, patients cross-over to hormonal therapy as in arm II.

* Arm II: Patients receive hormonal therapy comprising oral megestrol twice daily on weeks 1-3 followed by oral tamoxifen twice daily on weeks 4-6. Hormonal therapy repeats every 6 weeks in the absence of disease progression or unacceptable toxicity.

At time of disease progression, if patients have not previously been enrolled on arm I, patients cross-over to receive chemotherapy as in arm I.

Quality of life is assessed at baseline, 6 weeks, time of progression, and then after 6 weeks on cross-over therapy.

Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

PROJECTED ACCRUAL: Approximately 630 patients will be accrued for this study within 42 months.

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (50)

Jonsson Comprehensive Cancer Center, UCLA

🇺🇸

Los Angeles, California, United States

Rush-Presbyterian-St. Luke's Medical Center

🇺🇸

Chicago, Illinois, United States

Arthur G. James Cancer Hospital - Ohio State University

🇺🇸

Columbus, Ohio, United States

Fox Chase Cancer Center

🇺🇸

Philadelphia, Pennsylvania, United States

Indiana University Cancer Center

🇺🇸

Indianapolis, Indiana, United States

Fred Hutchinson Cancer Research Center

🇺🇸

Seattle, Washington, United States

University of Minnesota Cancer Center

🇺🇸

Minneapolis, Minnesota, United States

Duke Comprehensive Cancer Center

🇺🇸

Durham, North Carolina, United States

University of Mississippi Medical Center

🇺🇸

Jackson, Mississippi, United States

Cooper Hospital/University Medical Center

🇺🇸

Camden, New Jersey, United States

Cleveland Clinic Taussig Cancer Center

🇺🇸

Cleveland, Ohio, United States

Barbara Ann Karmanos Cancer Institute

🇺🇸

Detroit, Michigan, United States

University of Oklahoma College of Medicine

🇺🇸

Oklahoma City, Oklahoma, United States

Brookview Research, Inc.

🇺🇸

Nashville, Tennessee, United States

University of Alabama at Birmingham Comprehensive Cancer Center

🇺🇸

Birmingham, Alabama, United States

Chao Family Comprehensive Cancer Center

🇺🇸

Orange, California, United States

Community Hospital of Los Gatos

🇺🇸

Los Gatos, California, United States

University of Colorado Cancer Center

🇺🇸

Denver, Colorado, United States

H. Lee Moffitt Cancer Center and Research Institute

🇺🇸

Tampa, Florida, United States

Albert B. Chandler Medical Center, University of Kentucky

🇺🇸

Lexington, Kentucky, United States

Tufts University School of Medicine

🇺🇸

Boston, Massachusetts, United States

University of Massachusetts Memorial Medical Center

🇺🇸

Worcester, Massachusetts, United States

Mayo Clinic Cancer Center

🇺🇸

Rochester, Minnesota, United States

Ellis Fischel Cancer Center - Columbia

🇺🇸

Columbia, Missouri, United States

Cancer Center of Albany Medical Center

🇺🇸

Albany, New York, United States

State University of New York Health Science Center at Brooklyn

🇺🇸

Brooklyn, New York, United States

Roswell Park Cancer Institute

🇺🇸

Buffalo, New York, United States

State University of New York Health Sciences Center - Stony Brook

🇺🇸

Stony Brook, New York, United States

Memorial Sloan-Kettering Cancer Center

🇺🇸

New York, New York, United States

Comprehensive Cancer Center at Wake Forest University

🇺🇸

Winston-Salem, North Carolina, United States

Milton S. Hershey Medical Center

🇺🇸

Hershey, Pennsylvania, United States

Abington Memorial Hospital

🇺🇸

Abington, Pennsylvania, United States

Kimmel Cancer Center of Thomas Jefferson University - Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

Simmons Cancer Center - Dallas

🇺🇸

Dallas, Texas, United States

M.D. Anderson CCOP Research Base

🇺🇸

Houston, Texas, United States

Cancer Center at the University of Virginia

🇺🇸

Charlottesville, Virginia, United States

Fletcher Allen Health Care - Medical Center Campus

🇺🇸

Burlington, Vermont, United States

Tacoma General Hospital

🇺🇸

Tacoma, Washington, United States

Tom Baker Cancer Center - Calgary

🇨🇦

Calgary, Alberta, Canada

Ireland Cancer Center

🇺🇸

Cleveland, Ohio, United States

Barrett Cancer Center, The University Hospital

🇺🇸

Cincinnati, Ohio, United States

Holden Comprehensive Cancer Center at The University of Iowa

🇺🇸

Iowa City, Iowa, United States

Lineberger Comprehensive Cancer Center, UNC

🇺🇸

Chapel Hill, North Carolina, United States

University of Chicago Cancer Research Center

🇺🇸

Chicago, Illinois, United States

Washington University School of Medicine

🇺🇸

Saint Louis, Missouri, United States

Walter Reed Army Medical Center

🇺🇸

Washington, District of Columbia, United States

Schneider Children's Hospital at North Shore

🇺🇸

Manhasset, New York, United States

University of Pennsylvania Cancer Center

🇺🇸

Philadelphia, Pennsylvania, United States

University of Texas - MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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