- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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.
Panoramica dello studio
Descrizione dettagliata
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.
Tipo di studio
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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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, Stati Uniti, 35294
- University of Alabama Comprehensive Cancer Center
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Arizona
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Phoenix, Arizona, Stati Uniti, 85006-2726
- CCOP - Greater Phoenix
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California
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Los Angeles, California, Stati Uniti, 90033-0800
- USC/Norris Comprehensive Cancer Center
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Los Angeles, California, Stati Uniti, 90095-1781
- Jonsson Comprehensive Cancer Center, UCLA
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Orange, California, Stati Uniti, 92868
- Chao Family Comprehensive Cancer Center
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Palo Alto, California, Stati Uniti, 94304
- Women's Cancer Center
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Colorado
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Denver, Colorado, Stati Uniti, 80262
- University of Colorado Cancer Center
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District of Columbia
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Washington, District of Columbia, Stati Uniti, 20307-5000
- Walter Reed Army Medical Center
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Washington, District of Columbia, Stati Uniti, 20007
- Vincent T. Lombardi Cancer Research Center, Georgetown University
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Florida
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Tampa, Florida, Stati Uniti, 33612
- H. Lee Moffitt Cancer Center and Research Institute
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Georgia
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Atlanta, Georgia, Stati Uniti, 30322
- Emory University Hospital - Atlanta
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Hawaii
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Honolulu, Hawaii, Stati Uniti, 96813
- MBCCOP - Hawaii
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Illinois
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Chicago, Illinois, Stati Uniti, 60612-7323
- MBCCOP - University of Illinois at Chicago
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Chicago, Illinois, Stati Uniti, 60612
- Rush-Presbyterian-St. Luke's Medical Center
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Chicago, Illinois, Stati Uniti, 60637
- University of Chicago Cancer Research Center
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Decatur, Illinois, Stati Uniti, 62526
- CCOP - Central Illinois
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Evanston, Illinois, Stati Uniti, 60201
- CCOP - Evanston
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Indiana
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Indianapolis, Indiana, Stati Uniti, 46202-5265
- Indiana University Cancer Center
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Iowa
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Des Moines, Iowa, Stati Uniti, 50309-1016
- CCOP - Iowa Oncology Research Association
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Iowa City, Iowa, Stati Uniti, 52242
- University of Iowa Hospitals and Clinics
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Kentucky
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Lexington, Kentucky, Stati Uniti, 40536-0084
- Albert B. Chandler Medical Center, University of Kentucky
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Maryland
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Baltimore, Maryland, Stati Uniti, 21287
- Johns Hopkins Oncology Center
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Bethesda, Maryland, Stati Uniti, 20892
- Radiation Oncology Branch
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Bethesda, Maryland, Stati Uniti, 20892
- Medicine Branch
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02111
- Tufts University School of Medicine
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Worcester, Massachusetts, Stati Uniti, 01655
- University of Massachusetts Memorial Medical Center
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Michigan
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Ann Arbor, Michigan, Stati Uniti, 48106
- CCOP - Ann Arbor Regional
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Detroit, Michigan, Stati Uniti, 48201
- Barbara Ann Karmanos Cancer Institute
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Minnesota
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Minneapolis, Minnesota, Stati Uniti, 55455
- University of Minnesota Cancer Center
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Mississippi
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Jackson, Mississippi, Stati Uniti, 39216-4505
- University of Mississippi Medical Center
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Keesler AFB, Mississippi, Stati Uniti, 39534-2576
- Keesler Medical Center - Keesler AFB
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Missouri
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Kansas City, Missouri, Stati Uniti, 64131
- CCOP - Kansas City
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Saint Louis, Missouri, Stati Uniti, 63110
- Washington University School of Medicine
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Montana
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Billings, Montana, Stati Uniti, 59101
- CCOP - Montana Cancer Consortium
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Nebraska
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Omaha, Nebraska, Stati Uniti, 68131
- CCOP - Missouri Valley Cancer Consortium
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Nevada
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Las Vegas, Nevada, Stati Uniti, 89106
- CCOP - Southern Nevada Cancer Research Foundation
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New Jersey
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Camden, New Jersey, Stati Uniti, 08103
- Cooper Hospital/University Medical Center
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New York
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Albany, New York, Stati Uniti, 12208
- Cancer Center of Albany Medical Center
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Brooklyn, New York, Stati Uniti, 11203
- State University of New York Health Science Center at Brooklyn
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Manhasset, New York, Stati Uniti, 11030
- North Shore University Hospital
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New York, New York, Stati Uniti, 10021
- Memorial Sloan-Kettering Cancer Center
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Rochester, New York, Stati Uniti, 14642
- University of Rochester Cancer Center
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Stony Brook, New York, Stati Uniti, 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, Stati Uniti, 27599-7295
- Lineberger Comprehensive Cancer Center, UNC
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Durham, North Carolina, Stati Uniti, 27710
- Duke Comprehensive Cancer Center
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Winston-Salem, North Carolina, Stati Uniti, 27157-1082
- Comprehensive Cancer Center of Wake Forest University Baptist Medical Center
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Ohio
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Cincinnati, Ohio, Stati Uniti, 45219
- Barrett Cancer Center, The University Hospital
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Cleveland, Ohio, Stati Uniti, 44195
- Cleveland Clinic Cancer Center
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Cleveland, Ohio, Stati Uniti, 44106-5065
- Ireland Cancer Center
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Columbus, Ohio, Stati Uniti, 43210
- Arthur G. James Cancer Hospital - Ohio State University
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Oklahoma
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Oklahoma City, Oklahoma, Stati Uniti, 73190
- University of Oklahoma College of Medicine
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Tulsa, Oklahoma, Stati Uniti, 74136
- CCOP - Sooner State
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Oregon
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Portland, Oregon, Stati Uniti, 97213
- CCOP - Columbia River Program
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Pennsylvania
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Abington, Pennsylvania, Stati Uniti, 19001
- Abington Memorial Hospital
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Hershey, Pennsylvania, Stati Uniti, 17033
- Milton S. Hershey Medical Center
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Philadelphia, Pennsylvania, Stati Uniti, 19111
- Fox Chase Cancer Center
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Philadelphia, Pennsylvania, Stati Uniti, 19107
- Pennsylvania Hospital
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Philadelphia, Pennsylvania, Stati Uniti, 19104
- University of Pennsylvania Cancer Center
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Philadelphia, Pennsylvania, Stati Uniti, 19107
- Kimmel Cancer Center of Thomas Jefferson University - Philadelphia
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Wynnewood, Pennsylvania, Stati Uniti, 19096
- CCOP - MainLine Health
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South Carolina
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Charleston, South Carolina, Stati Uniti, 29425-0721
- Medical University of South Carolina
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Greenville, South Carolina, Stati Uniti, 29615
- CCOP - Greenville
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Spartanburg, South Carolina, Stati Uniti, 29303
- CCOP - Upstate Carolina
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Tennessee
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Memphis, Tennessee, Stati Uniti, 38117
- CCOP - Baptist Cancer Institute
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Nashville, Tennessee, Stati Uniti, 37203
- Brookview Research, Inc.
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Texas
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Dallas, Texas, Stati Uniti, 75235-9154
- Simmons Cancer Center - Dallas
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Houston, Texas, Stati Uniti, 77030
- University of Texas - MD Anderson Cancer Center
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Temple, Texas, Stati Uniti, 76508
- CCOP - Scott and White Hospital
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Virginia
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Charlottesville, Virginia, Stati Uniti, 22908
- Cancer Center, University of Virginia HSC
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Washington
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Seattle, Washington, Stati Uniti, 98195-6043
- University of Washington Medical Center
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Tacoma, Washington, Stati Uniti, 98405
- Tacoma General Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Cattedra di studio: Allan Covens, MD, Toronto Sunnybrook Regional Cancer Centre
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- CDR0000067139
- GOG-0180
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .