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Spots Global Cancer Trial Database for Oxaliplatin in Treating Patients With Persistent or Recurrent Endometrial Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Oxaliplatin in Treating Patients With Persistent or Recurrent Endometrial Cancer

Official Title: Phase II Evaluation of Oxaliplatin in the Treatment of Recurrent or Persistent Endometrial Carcinoma

Study ID: NCT00071929

Interventions

oxaliplatin

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, work in different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of oxaliplatin in treating patients who have persistent or recurrent endometrial cancer.

Detailed Description: OBJECTIVES: * Determine the antitumor activity of oxaliplatin in terms of response rate in patients with persistent or recurrent endometrial carcinoma that is refractory to curative or established therapy. * Determine the nature and degree of toxicity of this treatment regimen in these patients. OUTLINE: This is a multicenter study. Patients receive oxaliplatin IV over 2 hours on day 1. Treatment repeats every 3 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years and then every 6 months for 3 years. PROJECTED ACCRUAL: Approximately 19-51 patients will be accrued for this study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama, United States

CCOP - Western Regional, Arizona, Phoenix, Arizona, United States

Chao Family Comprehensive Cancer Center at University of California Irvine Cancer Center, Orange, California, United States

University of Colorado Cancer Center at University of Colorado Health Sciences Center, Denver, Colorado, United States

New Britain General Hospital, New Britain, Connecticut, United States

CCOP - Christiana Care Health Services, Newark, Delaware, United States

MBCCOP - University of Illinois at Chicago, Chicago, Illinois, United States

University of Chicago Cancer Research Center, Chicago, Illinois, United States

CCOP - Central Illinois, Decatur, Illinois, United States

CCOP - Evanston, Evanston, Illinois, United States

CCOP - Carle Cancer Center, Urbana, Illinois, United States

Saint Joseph Regional Medical Center, South Bend, Indiana, United States

Kansas Masonic Cancer Research Institute at the University of Kansas Medical Center, Kansas City, Kansas, United States

CCOP - Michigan Cancer Research Consortium, Ann Arbor, Michigan, United States

CCOP - Grand Rapids, Grand Rapids, Michigan, United States

CCOP - Kalamazoo, Kalamazoo, Michigan, United States

CCOP - Metro-Minnesota, Saint Louis Park, Minnesota, United States

University of Mississippi Medical Center, Jackson, Mississippi, United States

Ellis Fischel Cancer Center at University of Missouri - Columbia, Columbia, Missouri, United States

CCOP - Kansas City, Kansas City, Missouri, United States

CCOP - Cancer Research for the Ozarks, Springfield, Missouri, United States

CCOP - Missouri Valley Cancer Consortium, Omaha, Nebraska, United States

SUNY Downstate Medical Center, Brooklyn, New York, United States

Long Island Cancer Center at Stony Brook University Hospital, Stony Brook, New York, United States

Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill, Chapel Hill, North Carolina, United States

Ireland Cancer Center, Cleveland, Ohio, United States

Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, United States

Mount Carmel West Hospital, Columbus, Ohio, United States

University of Oklahoma College of Medicine, Oklahoma City, Oklahoma, United States

CCOP - Columbia River Oncology Program, Portland, Oregon, United States

Abington Memorial Hospital, Abington, Pennsylvania, United States

CCOP - Geisinger Clinic and Medical Center, Danville, Pennsylvania, United States

Penn State Cancer Institute at Milton S. Hershey Medical Center, Hershey, Pennsylvania, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

Magee-Womens Hospital, Pittsburgh, Pennsylvania, United States

Southeast Gynecologic Oncology Associates, Knoxville, Tennessee, United States

Vanderbilt-Ingram Cancer Center at Vanderbilt Medical Center, Nashville, Tennessee, United States

CCOP - Scott and White Hospital, Temple, Texas, United States

Contact Details

Name: Paula M. Fracasso, MD, PhD

Affiliation: Washington University Siteman Cancer Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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