Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

BMS-354825 in Treating Patients With Chronic Phase Chronic Myelogenous Leukemia That Is Resistant to Imatinib Mesylate

30 juli 2020 uppdaterad av: Jonsson Comprehensive Cancer Center

A Phase I Dose-Escalation Study To Determine The Safety, Pharmacokinetics, And Pharmacodynamics Of BMS-354825 In The Treatment Of Patients With Chronic Phase Chronic Myelogenous Leukemia Who Have Hematologic Resistance To Imatinib Mesylate (Gleevec

RATIONALE: BMS-354825 may stop the growth of cancer cells by stopping the enzymes necessary for cancer cell growth.

PURPOSE: This phase I trial is studying the side effects and best dose of BMS-354825 in treating patients with chronic phase chronic myelogenous leukemia that is resistant to imatinib mesylate.

Studieöversikt

Status

Avslutad

Betingelser

Intervention / Behandling

Detaljerad beskrivning

OBJECTIVES:

  • Determine the maximum tolerated dose, maximum administered dose, dose-limiting toxicity, and a recommended phase II dose of BMS-354825 in patients with chronic phase chronic myelogenous leukemia who have hematologic resistance to imatinib mesylate.
  • Determine the safety and tolerability of this drug in these patients.
  • Determine the plasma pharmacokinetics of this drug in these patients.
  • Determine, preliminarily, the efficacy of this drug, in terms of hematologic, cytogenetic, and molecular responses in these patients.

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

Patients receive oral BMS-354825 once daily on days 1-5. Courses repeat every 7 days for at least 3 months in the absence of disease progression or unacceptable toxicity. Patients may receive further treatment in the absence of disease progression.

Cohorts of 3-6 patients receive escalating doses of BMS-354825 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.

Once the MTD is determined, 20 additional patients receive treatment as in phase I at the MTD of BMS-354825.

Patients are followed for at least 30 days.

PROJECTED ACCRUAL: Approximately 50 patients (30 for phase I and 20 for phase II) will be accrued for this study within 12-18 months.

Studietyp

Interventionell

Inskrivning (Faktisk)

42

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • California
      • Los Angeles, California, Förenta staterna, 90095-1781
        • Jonsson Comprehensive Cancer Center at UCLA

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

INCLUSION CRITERIA:

  • Diagnosis of Philadelphia chromosome positive, chronic phase chronic myelogenous leukemia (CML) meeting all of the following criteria*:
  • Less than 15% blasts in peripheral blood and bone marrow
  • Less than 20% basophils in peripheral blood
  • Less than 30% blasts and promyelocytes in peripheral blood and bone marrow
  • Platelet count at least 100,000/mm^3 NOTE: *Patients who previously met the criteria for accelerated phase or blast phase CML, responded to treatment, and currently meet the criteria for chronic phase CML are eligible
  • Primary or acquired hematologic resistance to imatinib mesylate OR intolerance to imatinib mesylate defined as follows:
  • Primary hematologic resistance is defined as failure to reach complete hematologic response (CHR) with a dose of 400 mg/day continued for at least 3 months

    • Patients with hematological progression (i.e., WBC at least 10,000/mm^3 and rising consistently on at least 2 consecutive measurements obtained at least 14 days apart) while receiving imatinib mesylate of 400 mg/day are eligible if they have received less than 3 months of therapy
  • Acquired hematologic resistance is defined as achieving a CHR, but subsequently developing a rising WBC to at least 10,000/mm^3

    • WBC must be at least 10,000/mm^3 and rising on at least 2 measurements obtained at least 14 days apart with at least 1 of these measurements greater than 15,000/mm^3
  • Intolerance is defined as having discontinued imatinib mesylate due to nonhematologic toxicity of any grade

    • CD4^+ T-cell count at least 350/mm^3
  • 18 and over
  • ECOG 0-1
  • Life expectancy, At least 6 months.
  • Hepatic

    • Bilirubin no greater than 1.5 mg/dL
    • ALT and AST no greater than 2.0 times upper limit of normal (ULN)
  • Renal

    • Creatinine no greater than 1.5 times ULN
    • Potassium normal*
    • Magnesium normal*
    • Serum calcium or ionized calcium at least lower limit of normal NOTE: *Patients with low levels may be repleted to be eligible
  • Negative pregnancy test
  • Fertile patients must use effective contraception for 1 month before, during, and 1 month after study participation
  • More than 14 days since prior interferon
  • More than 14 days since prior cytarabine
  • More than 3 days since prior hydroxyurea
  • More than 28 days since other prior investigational or antineoplastic agents
  • More than 7 days since prior imatinib mesylate
  • At least 5 days or 5 half-lives since prior medications that inhibit platelet function, including the following:
  • Aspirin
  • Dipyridamole
  • Epoprostenol
  • Eptifibatide
  • Clopidogrel
  • Cilostazol
  • Abciximab
  • Ticlopidine
  • At least 5 days or 5 half-lives since prior anticoagulants such as warfarin or heparin/low molecular weight heparin (e.g., danaparoid, dalteparin, tinzaparin, enoxaparin)
  • At least 5 days or 5 half-lives since prior drugs accepted to have a risk of causing torsades de pointes, including the following:
  • Class IA antiarrhythmic agents (e.g., quinidine, procainamide, or disopyramide)
  • Class III antiarrhythmic agents (e.g., amiodarone, sotalol, ibutilide, or dofetilide)
  • Macrolide antibiotics (e.g., erythromycin or clarithromycin)
  • Antipsychotics (e.g., chlorpromazine, haloperidol, thioridazine, or pimozide)
  • Tricyclic antidepressants
  • Cisapride
  • Bepridil
  • Inapsine
  • Methadone
  • Arsenic
  • Concurrent anagrelide for thrombocytosis due to CML allowed

Exclusion Criteria:

  • extramedullary involvement (other than liver or spleen)
  • significant bleeding disorder unrelated to CML
  • acquired bleeding disorder within the past year (e.g., acquired antifactor VIII antibodies)
  • congenital bleeding disorders (e.g., von Willebrand disease)
  • uncontrolled or significant cardiovascular disease
  • uncontrolled angina within the past 6 months
  • congestive heart failure within the past 6 months
  • myocardial infarction within the past 12 months
  • history of clinically significant ventricular arrhythmias (e.g., ventricular tachycardia, ventricular fibrillation, or torsades de pointes)
  • history of second or third degree heart block (may be eligible if patient has a pacemaker)
  • diagnosed or suspected congenital long QT syndrome
  • prolonged QTc interval on pre-entry EKG (i.e., greater than 450 msec)
  • heart rate less than 50/minute on pre-entry EKG
  • uncontrolled hypertension
  • vasculitis
  • pregnant or nursing
  • gastrointestinal tract bleeding within the past 6 months
  • connective tissue disorders
  • other serious uncontrolled medical disorder or active infection that would impair the ability to receive study therapy
  • dementia or altered mental status that would preclude giving informed consent
  • evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, EKG, or clinical laboratory determinations unrelated to CML
  • prisoners or patients who are compulsorily detained (e.g., involuntary incarceration for treatment of either a psychiatric or physical [e.g., infectious disease] illness)
  • concurrent drugs accepted to have a risk of causing torsades de pointes
  • other concurrent treatment for CML
  • concurrent dolasetron or droperidol
  • concurrent anticoagulants
  • concurrent medications that inhibit platelet function

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Maskning: Ingen (Open Label)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Huvudutredare: Charles Sawyers, MD, Jonsson Comprehensive Cancer Center

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 november 2003

Primärt slutförande (Faktisk)

1 oktober 2006

Avslutad studie (Faktisk)

1 oktober 2006

Studieregistreringsdatum

Först inskickad

8 juli 2003

Först inskickad som uppfyllde QC-kriterierna

8 juli 2003

Första postat (Uppskatta)

9 juli 2003

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

3 augusti 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 juli 2020

Senast verifierad

1 augusti 2012

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera