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- Klinische proef NCT00003946
Danazol in Treating Patients With Advanced or Recurrent Endometrial Cancer
Phase II Study of Danazol in Advanced or Recurrent Endometrial Cancer
RATIONALE: Hormone therapy may be an effective treatment for endometrial cancer.
PURPOSE: Phase II trial to study the effectiveness of danazol in treating patients with advanced or recurrent endometrial cancer.
Studie Overzicht
Gedetailleerde beschrijving
OBJECTIVES: I. Assess the antitumor activity of danazol in patients with advanced or recurrent endometrial cancer. II. Determine the nature and toxicity of danazol in these patients.
OUTLINE: Patients receive oral danazol 4 times per day for at least 4 weeks. Patients with partial response, complete response, or stable disease continue treatment in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years, every 6 months for 2 years, and then annually thereafter.
PROJECTED ACCRUAL: A total of 23-56 patients will be accrued for this study within 26 months.
Studietype
Fase
- Fase 2
Contacten en locaties
Studie Locaties
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Ontario
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Kingston, Ontario, Canada, K7L 3N6
- NCIC-Clinical Trials Group
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Toronto, Ontario, Canada, M4N 3M5
- Toronto Sunnybrook Regional Cancer Centre
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Alabama
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Birmingham, Alabama, Verenigde Staten, 35294
- University of Alabama Comprehensive Cancer Center
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Arizona
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Phoenix, Arizona, Verenigde Staten, 85006-2726
- CCOP - Greater Phoenix
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California
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Los Angeles, California, Verenigde Staten, 90033-0800
- USC/Norris Comprehensive Cancer Center
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Los Angeles, California, Verenigde Staten, 90095-1781
- Jonsson Comprehensive Cancer Center, UCLA
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Orange, California, Verenigde Staten, 92868
- Chao Family Comprehensive Cancer Center
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Palo Alto, California, Verenigde Staten, 94304
- Women's Cancer Center
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Colorado
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Denver, Colorado, Verenigde Staten, 80262
- University of Colorado Cancer Center
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District of Columbia
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Washington, District of Columbia, Verenigde Staten, 20307-5000
- Walter Reed Army Medical Center
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Washington, District of Columbia, Verenigde Staten, 20007
- Vincent T. Lombardi Cancer Research Center, Georgetown University
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Florida
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Tampa, Florida, Verenigde Staten, 33612
- H. Lee Moffitt Cancer Center and Research Institute
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Georgia
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Atlanta, Georgia, Verenigde Staten, 30322
- Emory University Hospital - Atlanta
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Hawaii
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Honolulu, Hawaii, Verenigde Staten, 96813
- MBCCOP - Hawaii
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Illinois
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Chicago, Illinois, Verenigde Staten, 60612-7323
- MBCCOP - University of Illinois at Chicago
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Chicago, Illinois, Verenigde Staten, 60612
- Rush-Presbyterian-St. Luke's Medical Center
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Chicago, Illinois, Verenigde Staten, 60637
- University of Chicago Cancer Research Center
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Decatur, Illinois, Verenigde Staten, 62526
- CCOP - Central Illinois
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Evanston, Illinois, Verenigde Staten, 60201
- CCOP - Evanston
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Indiana
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Indianapolis, Indiana, Verenigde Staten, 46202-5265
- Indiana University Cancer Center
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Iowa
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Des Moines, Iowa, Verenigde Staten, 50309-1016
- CCOP - Iowa Oncology Research Association
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Iowa City, Iowa, Verenigde Staten, 52242
- University of Iowa Hospitals and Clinics
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Kentucky
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Lexington, Kentucky, Verenigde Staten, 40536-0084
- Albert B. Chandler Medical Center, University of Kentucky
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Maryland
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Baltimore, Maryland, Verenigde Staten, 21287
- Johns Hopkins Oncology Center
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Bethesda, Maryland, Verenigde Staten, 20892
- Radiation Oncology Branch
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Bethesda, Maryland, Verenigde Staten, 20892
- Medicine Branch
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Massachusetts
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Boston, Massachusetts, Verenigde Staten, 02111
- Tufts University School of Medicine
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Worcester, Massachusetts, Verenigde Staten, 01655
- University of Massachusetts Memorial Medical Center
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Michigan
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Ann Arbor, Michigan, Verenigde Staten, 48106
- CCOP - Ann Arbor Regional
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Detroit, Michigan, Verenigde Staten, 48201
- Barbara Ann Karmanos Cancer Institute
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Minnesota
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Minneapolis, Minnesota, Verenigde Staten, 55455
- University of Minnesota Cancer Center
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Mississippi
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Jackson, Mississippi, Verenigde Staten, 39216-4505
- University of Mississippi Medical Center
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Keesler AFB, Mississippi, Verenigde Staten, 39534-2576
- Keesler Medical Center - Keesler AFB
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Missouri
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Kansas City, Missouri, Verenigde Staten, 64131
- CCOP - Kansas City
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Saint Louis, Missouri, Verenigde Staten, 63110
- Washington University School of Medicine
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Montana
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Billings, Montana, Verenigde Staten, 59101
- CCOP - Montana Cancer Consortium
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Nebraska
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Omaha, Nebraska, Verenigde Staten, 68131
- CCOP - Missouri Valley Cancer Consortium
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Nevada
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Las Vegas, Nevada, Verenigde Staten, 89106
- CCOP - Southern Nevada Cancer Research Foundation
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New Jersey
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Camden, New Jersey, Verenigde Staten, 08103
- Cooper Hospital/University Medical Center
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New York
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Albany, New York, Verenigde Staten, 12208
- Cancer Center of Albany Medical Center
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Brooklyn, New York, Verenigde Staten, 11203
- State University of New York Health Science Center at Brooklyn
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Manhasset, New York, Verenigde Staten, 11030
- North Shore University Hospital
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New York, New York, Verenigde Staten, 10021
- Memorial Sloan-Kettering Cancer Center
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Rochester, New York, Verenigde Staten, 14642
- University of Rochester Cancer Center
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Stony Brook, New York, Verenigde Staten, 11790-9832
- State University of New York Health Sciences Center - Stony Brook
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North Carolina
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Chapel Hill, North Carolina, Verenigde Staten, 27599-7295
- Lineberger Comprehensive Cancer Center, UNC
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Durham, North Carolina, Verenigde Staten, 27710
- Duke Comprehensive Cancer Center
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Winston-Salem, North Carolina, Verenigde Staten, 27157-1082
- Comprehensive Cancer Center of Wake Forest University Baptist Medical Center
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Ohio
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Cincinnati, Ohio, Verenigde Staten, 45219
- Barrett Cancer Center, The University Hospital
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Cleveland, Ohio, Verenigde Staten, 44195
- Cleveland Clinic Cancer Center
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Cleveland, Ohio, Verenigde Staten, 44106-5065
- Ireland Cancer Center
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Columbus, Ohio, Verenigde Staten, 43210
- Arthur G. James Cancer Hospital - Ohio State University
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Oklahoma
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Oklahoma City, Oklahoma, Verenigde Staten, 73190
- University of Oklahoma College of Medicine
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Tulsa, Oklahoma, Verenigde Staten, 74136
- CCOP - Sooner State
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Oregon
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Portland, Oregon, Verenigde Staten, 97213
- CCOP - Columbia River Program
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Pennsylvania
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Abington, Pennsylvania, Verenigde Staten, 19001
- Abington Memorial Hospital
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Hershey, Pennsylvania, Verenigde Staten, 17033
- Milton S. Hershey Medical Center
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Philadelphia, Pennsylvania, Verenigde Staten, 19111
- Fox Chase Cancer Center
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Philadelphia, Pennsylvania, Verenigde Staten, 19107
- Pennsylvania Hospital
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Philadelphia, Pennsylvania, Verenigde Staten, 19104
- University of Pennsylvania Cancer Center
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Philadelphia, Pennsylvania, Verenigde Staten, 19107
- Kimmel Cancer Center of Thomas Jefferson University - Philadelphia
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Wynnewood, Pennsylvania, Verenigde Staten, 19096
- CCOP - MainLine Health
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South Carolina
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Charleston, South Carolina, Verenigde Staten, 29425-0721
- Medical University of South Carolina
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Greenville, South Carolina, Verenigde Staten, 29615
- CCOP - Greenville
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Spartanburg, South Carolina, Verenigde Staten, 29303
- CCOP - Upstate Carolina
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Tennessee
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Memphis, Tennessee, Verenigde Staten, 38117
- CCOP - Baptist Cancer Institute
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Nashville, Tennessee, Verenigde Staten, 37203
- Brookview Research, Inc.
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Texas
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Dallas, Texas, Verenigde Staten, 75235-9154
- Simmons Cancer Center - Dallas
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Houston, Texas, Verenigde Staten, 77030
- University of Texas - MD Anderson Cancer Center
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Temple, Texas, Verenigde Staten, 76508
- CCOP - Scott and White Hospital
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Virginia
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Charlottesville, Virginia, Verenigde Staten, 22908
- Cancer Center, University of Virginia HSC
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Washington
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Seattle, Washington, Verenigde Staten, 98195-6043
- University of Washington Medical Center
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Tacoma, Washington, Verenigde Staten, 98405
- Tacoma General Hospital
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
DISEASE CHARACTERISTICS: Histologically proven advanced or recurrent endometrial cancer that is not amenable to curative surgery or radiotherapy Measurable disease Tumor at least 1.0 cm by 1.0 cm per x-ray or physical exam OR Tumor at least 2.0 cm by 2.0 cm per CT scan, MRI, or ultrasound
PATIENT CHARACTERISTICS: Age: Not specified Performance status: GOG 0-2 Life expectancy: Not specified Hematopoietic: WBC at least 3000/mm3 Platelet count at least 100,000/mm3 No history of porphyria Hepatic: Bilirubin no greater than 1.5 times normal SGOT no greater than 3 times normal Alkaline phosphatase no greater than 3 times normal Renal: Creatinine no greater than 2 mg/dL Other: No concurrent or prior malignancy within past 5 years (except nonmelanoma skin cancer) or for which patient received chemotherapy Not pregnant or nursing Fertile patients must use effective contraception Must have tissue available for estrogen receptor/ progesterone receptor analysis
PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior chemotherapy Endocrine therapy: Not specified Radiotherapy: At least 3 weeks since prior radiotherapy and recovered Surgery: At least 3 weeks since prior surgery and recovered
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
Medewerkers en onderzoekers
Sponsor
Medewerkers
Onderzoekers
- Studie stoel: Allan Covens, MD, Toronto Sunnybrook Regional Cancer Centre
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- CDR0000067139
- GOG-0180
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .