- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00652691
Topotecan, High-Dose Cyclophosphamide, Carboplatin, and an Autologous Peripheral Blood Cell Transplant in Treating Patients With Recurrent Ovarian Cancer or Primary Peritoneal Cancer
A Dose Seeking Trial of Topotecan Combined With High-Dose Cyclophosphamide and Carboplatin With Peripheral Blood Stem Cell Transplant for the Treatment of Relapsed Ovarian Cancer and Primary Peritoneal Cancer
RATIONALE: Giving colony-stimulating factors, such as G-CSF help stem cells move from the patient's bone marrow to the blood so they can be collected and stored. Combination chemotherapy is then given to prepare the bone marrow for the stem cell transplant. The stem cells are returned to the patient to replace the blood-forming cells that were destroyed by the chemotherapy.
PURPOSE: This randomized trial is studying the side effects and best dose of topotecan when given together with high-dose cyclophosphamide, and carboplatin followed by an autologous peripheral blood stem cell transplant in treating patients with recurrent ovarian cancer or primary peritoneal cancer.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
OBJECTIVES:
- To determine the maximum tolerated dose of topotecan hydrochloride combined with high-dose cyclophosphamide and carboplatin in the setting of autologous peripheral blood stem cell transplantation for relapsed, recurrent, or persistent ovarian epithelial or primary peritoneal cavity cancer.
- To assess the toxicity of this regimen.
OUTLINE: This is a dose escalation study of topotecan.
- Autologous hematopoietic stem cell collection: Patients receive filgrastim subcutaneously (SC) daily for 5 days. Patients undergo leukapheresis per standard practice until a minimum of 2 x10^6 CD34+ cells/kg are collected and cryopreserved.
- High-dose chemotherapy: Patients receive topotecan hydrochloride IV, cyclophosphamide IV, and carboplatin IV over 8 hours on days -6 to -3.
- Autologous peripheral stem cell reinfusion: Patients undergo autologous peripheral blood stem cell transplantation on day 0. Patients also receive sargramostim SC daily beginning on day 5 and continuing until blood counts recover.
After completion of study therapy, patients are followed monthly for 3 months, every 3 months for 2 years, and then every 6 months for 5 years.
Studietype
Registrering (Forventet)
Fase
- Fase 1
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
DISEASE CHARACTERISTICS:
Histologically confirmed ovarian epithelial or primary peritoneal cavity cancer
Recurrent, relapsed, or persistent disease meeting 1 or more of the following criteria:
- Patients with a positive second-look laparotomy who are not candidates for higher priority GOG protocols
- Largest mass of recurrent disease ≤ 0.2 cm achieved by surgery or chemotherapy
- Achievement of complete response to 1 prior regimen of platinum-based chemotherapy with relapse > 6 months from last chemotherapy
- Achievement of partial response to 1 platinum-based chemotherapy regimen prior to study
- Histological proof of disease recurrence with or without a rising serum CA-125 level (relapsed or recurrent disease)
The following histological cell types are allowed:
- Clear-cell adenocarcinoma
- Endometrioid adenocarcinoma
- Mixed epithelial carcinoma
- Mucinous adenocarcinoma
- Serous adenocarcinoma
- Undifferentiated carcinoma
- Must have unilateral bone marrow aspirate and biopsy with cytogenetics without evidence of metastatic ovarian carcinoma by conventional morphology within 1 month of registration
- Not eligible for GOG-164
PATIENT CHARACTERISTICS:
- ECOG performance status 0-2
- Creatinine ≤ 1.5 mg/dL
- Total bilirubin ≤ 2.0 mg/dL (≤ 5.0 mg/dL with metastatic disease)
- AST ≤ 2 times upper limit of normal (ULN) (≤ 600 units/mL with metastatic disease)
- Alkaline phosphatase ≤ 2 times ULN (unless related to metastatic disease)
- ANC ≥ 1,000/mm^3
- Platelets ≥ 100,000/mm^3
- Cardiac ejection fraction ≥ 45% by rest ECHO or MUGA
- FEV_1 ≥ 50% of predicted
- HIV negative
- No uncontrolled infection
No severe medical or psychiatric illness, including any of the following:
- Renal failure
- Brittle insulin dependent diabetes mellitus
- Congestive heart failure
- History of myocardial infarction within the past 3 months
- Significant arrhythmia requiring medication
- Poorly controlled hypertension (diastolic blood pressure >100 mm Hg)
- History of hospitalization for severe depression or psychosis
- Significant non-neoplastic pulmonary disease
- Current alcohol or drug abuse.
- Active infection
- Active peptic ulcer disease
- No prior malignancy within the past 5 years except adequately treated basal cell or squamous cell carcinoma of the skin or in situ cervical carcinoma
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No more than 1 prior treatment regimen for this cancer
- More than 3 weeks since surgery
- No prior topotecan hydrochloride
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
Hva måler studien?
Primære resultatmål
Resultatmål |
---|
Maximum tolerated dose of topotecan hydrochloride
|
Toxicity according to NCI criteria
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Studiestol: Mark R. Litzow, MD, Mayo Clinic
- Hovedetterforsker: Lawrence A Solberg, M.D., Mayo Clinic
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Neoplasmer etter histologisk type
- Neoplasmer
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Karsinom
- Neoplasmer, kjertel og epitel
- Genitale neoplasmer, kvinnelige
- Sykdommer i det endokrine systemet
- Sykdommer i eggstokkene
- Adnexal sykdommer
- Gonadal lidelser
- Neoplasmer i endokrine kjertel
- Neoplasmer i eggstokkene
- Karsinom, ovarieepitel
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Enzymhemmere
- Antirevmatiske midler
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Antineoplastiske midler, Alkylering
- Alkyleringsmidler
- Myeloablative agonister
- Topoisomerasehemmere
- Topoisomerase I-hemmere
- Cyklofosfamid
- Karboplatin
- Topotekan
Andre studie-ID-numre
- 976101 (Annen identifikator: Mayo Clinic Cancer Center)
- P30CA015083 (U.S. NIH-stipend/kontrakt)
- 1056-98 (Annen identifikator: Mayo Clinic IRB)
Legemiddel- og utstyrsinformasjon, studiedokumenter
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