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Topotecan, High-Dose Cyclophosphamide, Carboplatin, and an Autologous Peripheral Blood Cell Transplant in Treating Patients With Recurrent Ovarian Cancer or Primary Peritoneal Cancer

4. april 2019 oppdatert av: Mayo Clinic

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

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

Intervensjonell

Registrering (Forventet)

48

Fase

  • Fase 1

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 70 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

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

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Etterforskere

  • Studiestol: Mark R. Litzow, MD, Mayo Clinic
  • Hovedetterforsker: Lawrence A Solberg, M.D., Mayo Clinic

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. august 1998

Primær fullføring (Faktiske)

5. juni 2002

Studiet fullført (Faktiske)

4. mai 2016

Datoer for studieregistrering

Først innsendt

3. april 2008

Først innsendt som oppfylte QC-kriteriene

3. april 2008

Først lagt ut (Anslag)

4. april 2008

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

8. april 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. april 2019

Sist bekreftet

1. mars 2018

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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