Decentrialz logo
  • HIPAA Compliant
  • ISO 27001 Certified
Find Trials
About UsContact
Become a Volunteer+1 877 705 1914

Status:

UNKNOWN

VNP40101M Followed by Cytarabine in Treating Older Patients With Acute Myeloid Leukemia

Lead Sponsor:

Vion Pharmaceuticals

Conditions:

Leukemia

Eligibility:

All Genders

60+ years

Phase:

PHASE2

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as VNP40101M and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Givin...

Detailed Description

OBJECTIVES: Primary * Determine the complete response rate in older patients with poor-risk, de novo acute myeloid leukemia treated with VNP40101M as induction therapy followed by cytarabine as cons...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed de novo acute myeloid leukemia (AML)
  • No acute promyelocytic leukemia \[t(15;17)\]
  • No favorable cytogenetics, including t(15;17), t(8;21), or inv 16
  • No secondary AML, defined as having a history of an antecedent hematologic disorder (myelodysplastic syndromes \[MDS\] or myeloproliferative disease), or history of prior chemotherapy or radiation for a disease other than AML
  • Must have ≥ 1 of the following poor-risk features:
  • Any of the following unfavorable cytogenetics:
  • Del (5q)/-5q
  • -7/del(7q)
  • Abnormal 3q, 9q, 11q, 20q, 21q, or 17p
  • t(6;9)
  • t(9;22)
  • Trisomy 8
  • Complex karyotypes (≥ 3 unrelated abnormalities)
  • At least 70 years of age
  • ECOG performance status (PS) of 2
  • Cardiac dysfunction\* that would limit the use of anthracycline therapy, as defined by any of the following:
  • Ejection fraction ≤ 50%
  • History of significant coronary artery disease, defined as ≥ 1 vessel stenosis requiring medical treatment, stent placement, or surgical bypass graft
  • History of congestive heart failure or myocardial infarction
  • Significant arrhythmia, including any of the following:
  • Atrial flutter (excluding atrial fibrillation)
  • Sick sinus syndrome
  • Ventricular arrhythmia
  • Heart valve disease
  • Mitral valve prolapse allowed
  • Other heart disease, at the discretion of the principal investigator
  • Pulmonary dysfunction not related to AML, defined by 1 of the following:
  • DLCO and/or FEV\_1 \< 80% and ≥ 50% normal range
  • Dyspnea on slight activity or at rest
  • Requires oxygen
  • Hepatic dysfunction related to chronic hepatitis or liver cirrhosis
  • Other organ dysfunction or comorbidity that precludes standard cytotoxic induction treatment (e.g., "3+7"), at the discretion of the principal investigator NOTE: \*Patients with a history of heart disease as defined above must be on appropriate medication and have their disease under control
  • No known CNS disease
  • PATIENT CHARACTERISTICS:
  • ECOG PS 0-2
  • AST and ALT ≤ 5 times upper limit of normal
  • Bilirubin ≤ 2.0 mg/dL
  • Creatinine ≤ 2.0 mg/dL
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 6 months after completion of study treatment
  • No active, uncontrolled infection
  • Patients with an infection who are under active treatment with antibiotics and whose infections are controlled are eligible
  • Chronic hepatitis allowed
  • No clinical evidence of ongoing second malignancy unrelated to AML or MDS
  • No evidence of left bundle branch block on screening ECG
  • No obligate use of cardiac pacemaker or atrial fibrillation
  • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • At least 24 hours since prior metronidazole
  • No prior low-dose, single-agent, cytotoxic chemotherapy (e.g., cytarabine, decitabine, or azacitidine)
  • No concurrent disulfiram
  • No other concurrent standard or investigational therapy for AML except for the following:
  • Concurrent hydroxyurea to control rising white blood cell counts
  • Dosage must be 4-6 grams daily for up to 4 days
  • Concurrent leukapheresis to control blast cell counts
  • Must be completed within the first 5 days of study therapy
  • No more than 2 procedures per day or 4 procedures total
  • Investigational supportive care agents (e.g., antimicrobials or antifungal agents), at the discretion of the protocol sponsor

Exclusion

    Key Trial Info

    Start Date :

    May 1 2006

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    Estimated Enrollment :

    85 Patients enrolled

    Trial Details

    Trial ID

    NCT00354276

    Start Date

    May 1 2006

    Last Update

    January 10 2014

    Active Locations (3)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (3 locations)

    1

    Jonsson Comprehensive Cancer Center at UCLA

    Los Angeles, California, United States, 90095-1781

    2

    Hopital Haut Leveque

    Pessac, France, 33604

    3

    University Hospital of Wales

    Cardiff, Wales, United Kingdom, CF14 4XW