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OSI-7904L and Oxaliplatin in Treating Patients With Refractory or Recurrent Advanced Colorectal Cancer

A Phase I Study of OSI-7904L In Combination With Oxaliplatin In Patients With Advanced Colo-Rectal Cancer

RATIONALE: OSI-7904L may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Drugs used in chemotherapy, such as oxaliplatin, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining OSI-7904L with oxaliplatin may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of OSI-7904L and oxaliplatin in treating patients with refractory or recurrent advanced colorectal cancer.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

OBJECTIVES:

Primary

  • Determine the dose-limiting toxicity of OSI-7904L and oxaliplatin in patients with refractory or recurrent advanced colorectal cancer.
  • Determine the maximum tolerated dose of this regimen in these patients.
  • Determine a safe dose for this regimen in these patients.

Secondary

  • Determine the pharmacokinetic profile of this regimen in these patients.
  • Determine the safety profile of this regimen in these patients.
  • Determine the antitumor activity of this regimen in these patients.

OUTLINE: This is a nonrandomized, multicenter, open-label, dose-escalation study.

Patients receive oxaliplatin IV over 2 hours followed by OSI-7904L IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of OSI-7904L and oxaliplatin until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity. A maximum of 12 patients receive treatment at the MTD.

Patients are followed every 8 weeks.

PROJECTED ACCRUAL: A total of 3-25 patients will be accrued for this study.

Studietype

Intervensjonell

Registrering (Faktiske)

15

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • England
      • Manchester, England, Storbritannia, M20 4BX
        • Christie Hospital N.H.S. Trust
      • Hannover, Tyskland, D-30625
        • Medizinische Hochschule Hannover

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 og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

DISEASE CHARACTERISTICS:

  • Histologically confirmed colorectal cancer

    • Radiologic evidence of advanced disease
  • At least 1 measurable lesion at least 20 mm OR at least 10 mm by spiral CT scan

    • Indicator lesions in a previously irradiated field are allowed provided the irradiated lesion has clearly progressed OR a new lesion has developed in the irradiated field
  • Failed 1, and only 1, line of prior chemotherapy for advanced/metastatic disease

    • Disease progression during chemotherapy OR within 6 months after completion of treatment
  • No symptomatic brain metastases meeting any of the following criteria:

    • Unstable
    • Inadequately controlled with fixed-dose oral steroids
    • Potentially life-threatening
    • Required radiotherapy with the past 28 days

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • ECOG 0-2

Life expectancy

  • Not specified

Hematopoietic

  • Neutrophil count > 1,500/mm^3
  • Platelet count > 100,000/mm^3

Hepatic

  • AST and ALT < 2.5 times upper limit of normal (ULN) (5 times ULN if liver metastases are present)
  • Bilirubin < 1.5 times ULN
  • No hepatitis
  • No cirrhosis

Renal

  • Creatinine < 1.5 times ULN

Other

  • Not pregnant
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 months after study participation
  • HIV negative
  • No preexisting neuropathy ≥ grade 2
  • No active or uncontrolled infection
  • No other serious illness or medical condition
  • No chronic alcohol abuse
  • No known hypersensitivity to systemic liposomal formulations or compounds chemically related to OSI-7904L or oxaliplatin
  • No prior psychiatric or neurologic condition that would preclude study compliance or giving informed consent

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • At least 21 days since prior immunotherapy
  • At least 21 days since prior monoclonal antibody therapy

Chemotherapy

  • See Disease Characteristics
  • At least 21 days since prior chemotherapy and recovered*
  • No prior oxaliplatin NOTE: *Alopecia allowed

Endocrine therapy

  • See Disease Characteristics
  • At least 21 days since prior hormonal therapy

Radiotherapy

  • See Disease Characteristics
  • At least 21 days since prior radiotherapy and recovered
  • No prior radiotherapy to more than 25% of bone marrow reserve

Surgery

  • Recovered from prior surgery

Other

  • At least 21 days since prior tyrosine kinase inhibitor therapy
  • More than 21 days since prior investigational agents
  • No other concurrent anticancer therapy
  • No other concurrent investigational agents

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Masking: Ingen (Open Label)

Hva måler studien?

Primære resultatmål

Resultatmål
Maximum tolerated dose and recommended dose for future trials as measured by CTC v3.0

Sekundære resultatmål

Resultatmål
Safety profile as measured by CTC v3.0
Response as measured by RECIST every 6 weeks (2 courses)
Pharmacodynamics as measured by drug concentration in the blood during course 1
Time to progression as measured by Kaplan Meier and RECIST every 6 weeks during treatment and then every 8 weeks

Samarbeidspartnere og etterforskere

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

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

1. februar 2004

Primær fullføring (Faktiske)

1. august 2005

Datoer for studieregistrering

Først innsendt

7. april 2004

Først innsendt som oppfylte QC-kriteriene

7. april 2004

Først lagt ut (Anslag)

8. april 2004

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

12. juni 2013

Siste oppdatering sendt inn som oppfylte QC-kriteriene

11. juni 2013

Sist bekreftet

1. juni 2013

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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