- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00003156
Topotecan in Treating Patients With Recurrent or Refractory Cancer of the Uterus
Evaluation of Topotecan in the Treatment of Persistent or Recurrent Carcinosarcoma (Mixed Mesodermal Tumors) of the Uterus
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 topotecan in treating patients with recurrent or refractory cancer of the uterus.
Studieoversikt
Detaljert beskrivelse
OBJECTIVES: I. Estimate the antitumor activity of topotecan in patients with recurrent or refractory carcinosarcoma of the uterus who have failed standard therapy. II. Determine the nature and degree of toxic effects of topotecan in these patients.
OUTLINE: Patients receive topotecan IV over 30 minutes daily for 5 days. Treatment repeats every 3 weeks for a minimum of 1 course in the absence of disease progression or unacceptable toxicity. Patients with complete response, partial response, or stable disease continue treatment for at least three courses. Patients are followed every 4 months for 2 years, every 6 months for 3 years, and then periodically thereafter until death.
PROJECTED ACCRUAL: Approximately 25-40 patients will be accrued for this study within 2 years.
Studietype
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
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Alberta
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Calgary, Alberta, Canada, T2N 4N2
- Tom Baker Cancer Center - Calgary
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Alabama
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Birmingham, Alabama, Forente stater, 35294
- University of Alabama Comprehensive Cancer Center
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California
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Los Angeles, California, Forente stater, 90095-1781
- Jonsson Comprehensive Cancer Center, UCLA
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Los Gatos, California, Forente stater, 95032
- Community Hospital of Los Gatos
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Orange, California, Forente stater, 92868
- Chao Family Comprehensive Cancer Center
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District of Columbia
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Washington, District of Columbia, Forente stater, 20307-5000
- Walter Reed Army Medical Center
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Florida
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Tampa, Florida, Forente stater, 33612
- H. Lee Moffitt Cancer Center and Research Institute
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Illinois
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Chicago, Illinois, Forente stater, 60612
- Rush-Presbyterian-St. Luke's Medical Center
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Chicago, Illinois, Forente stater, 60637
- University of Chicago Cancer Research Center
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Indiana
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Indianapolis, Indiana, Forente stater, 46202-5265
- Indiana University Cancer Center
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Iowa
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Iowa City, Iowa, Forente stater, 52242
- University of Iowa Hospitals and Clinics
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Maryland
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Bethesda, Maryland, Forente stater, 20892
- Radiation Oncology Branch
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Massachusetts
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Boston, Massachusetts, Forente stater, 02111
- Tufts University School of Medicine
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Michigan
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Detroit, Michigan, Forente stater, 48201
- Barbara Ann Karmanos Cancer Institute
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Minnesota
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Minneapolis, Minnesota, Forente stater, 55455
- University of Minnesota Cancer Center
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Mississippi
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Jackson, Mississippi, Forente stater, 39216-4505
- University of Mississippi Medical Center
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Missouri
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Columbia, Missouri, Forente stater, 65203
- Ellis Fischel Cancer Center - Columbia
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Kansas City, Missouri, Forente stater, 64131
- CCOP - Kansas City
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Saint Louis, Missouri, Forente stater, 63110
- Washington University School of Medicine
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New York
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Albany, New York, Forente stater, 12208
- Cancer Center of Albany Medical Center
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Brooklyn, New York, Forente stater, 11203
- State University of New York Health Science Center at Brooklyn
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Manhasset, New York, Forente stater, 11030
- North Shore University Hospital
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Stony Brook, New York, Forente stater, 11790-7775
- State University of New York Health Sciences Center - Stony Brook
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North Carolina
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Chapel Hill, North Carolina, Forente stater, 27599-7295
- Lineberger Comprehensive Cancer Center, UNC
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Durham, North Carolina, Forente stater, 27710
- Duke Comprehensive Cancer Center
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Winston-Salem, North Carolina, Forente stater, 27157-1082
- Comprehensive Cancer Center of Wake Forest University Baptist Medical Center
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Ohio
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Cincinnati, Ohio, Forente stater, 45219
- Barrett Cancer Center, The University Hospital
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Cleveland, Ohio, Forente stater, 44195
- Cleveland Clinic Taussig Cancer Center
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Cleveland, Ohio, Forente stater, 44106-5065
- Ireland Cancer Center
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Columbus, Ohio, Forente stater, 43210
- Arthur G. James Cancer Hospital - Ohio State University
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Oklahoma
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Oklahoma City, Oklahoma, Forente stater, 73190
- University of Oklahoma College of Medicine
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Tulsa, Oklahoma, Forente stater, 74136
- CCOP - Sooner State
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Pennsylvania
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Abington, Pennsylvania, Forente stater, 19001
- Abington Memorial Hospital
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Hershey, Pennsylvania, Forente stater, 17033
- Milton S. Hershey Medical Center
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Philadelphia, Pennsylvania, Forente stater, 19111
- Fox Chase Cancer Center
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Philadelphia, Pennsylvania, Forente stater, 19104
- University of Pennsylvania Cancer Center
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Wynnewood, Pennsylvania, Forente stater, 19096
- CCOP - MainLine Health
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South Carolina
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Spartanburg, South Carolina, Forente stater, 29303
- CCOP - Upstate Carolina
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Tennessee
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Memphis, Tennessee, Forente stater, 38117
- CCOP - Baptist Cancer Institute
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Nashville, Tennessee, Forente stater, 37203
- Brookview Research, Inc.
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Texas
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Dallas, Texas, Forente stater, 75235-9154
- Simmons Cancer Center - Dallas
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Temple, Texas, Forente stater, 76508
- CCOP - Scott and White Hospital
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Vermont
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Burlington, Vermont, Forente stater, 05401
- Fletcher Allen Health Care
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Virginia
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Charlottesville, Virginia, Forente stater, 22908
- Cancer Center, University of Virginia HSC
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Washington
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Seattle, Washington, Forente stater, 98195-6043
- University of Washington Medical Center
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Tacoma, Washington, Forente stater, 98405
- Tacoma General Hospital
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
DISEASE CHARACTERISTICS: Histologically proven recurrent or refractory carcinosarcoma (mixed mesodermal tumors) of the uterus Measurable disease
PATIENT CHARACTERISTICS: Age: Not specified Performance Status: GOG 0-2 Life Expectancy: Not specified Hematopoietic: Platelet count at least 100,000/mm3 Absolute granulocyte count at least 1,500/mm3 Hepatic: Bilirubin no greater than 1.5 times upper limit of normal (ULN) SGOT no greater than 3 times ULN Alkaline phosphatase no greater than 3 times ULN Renal: Creatinine no greater than 1.5 mg/dL Creatinine clearance greater than 20 mL/min Other: No invasive malignancies within the past 5 years except nonmelanomatous skin cancer No significant infection
PRIOR CONCURRENT THERAPY: Biologic therapy: At least 3 weeks since prior biologic therapy Chemotherapy: At least 3 weeks since prior chemotherapy and recovered No prior topotecan or camptothecin therapy No more than 1 prior chemotherapy regimen (either single or combination chemotherapy) Endocrine therapy: At least 3 weeks since prior endocrine therapy Radiotherapy: At least 3 weeks since prior radiotherapy and recovered Surgery: Prior surgery allowed and recovered
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CDR0000065948
- GOG-130D
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