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Spots Global Cancer Trial Database for VNP40101M Followed by Cytarabine in Treating Older Patients With Acute Myeloid Leukemia

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Trial Identification

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

Official Title: A Phase II Study of Cloretazine® (VNP40101M) for Elderly Patients With De Novo Poor Risk Acute Myelogenous Leukemia

Study ID: NCT00354276

Conditions

Leukemia

Study Description

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. Giving VNP40101M followed by cytarabine may kill more cancer cells. PURPOSE: This phase II trial is studying how well VNP40101M followed by cytarabine works in treating older patients with acute myeloid leukemia.

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 consolidation therapy. Secondary * Determine the probability of overall survival, leukemia-free survival, and progression-free survival of patients treated with this regimen. * Determine the safety of this regimen in these patients. OUTLINE: This is an open-label, multicenter study. * Induction therapy: Patients receive VNP40101M IV over 60 minutes on day 1 (course 1). Patients without evidence of disease progression who have responding but residual disease receive a second course of VNP40101M once between days 35-60. Patients achieving complete response or partial response after induction therapy proceed to consolidation therapy. * Consolidation therapy: Beginning between days 45-90, patients receive cytarabine IV continuously over 5 days (course 1). Patients may receive a second course of cytarabine at the discretion of the investigator. After completion of study treatment, patients are followed periodically for up to 36 months. PROJECTED ACCRUAL: A total of 85 patients will be accrued for this study.

Eligibility

Minimum Age: 60 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Jonsson Comprehensive Cancer Center at UCLA, Los Angeles, California, United States

Hopital Haut Leveque, Pessac, , France

University Hospital of Wales, Cardiff, Wales, United Kingdom

Contact Details

Name: Bonny L. Johnson, RN, MSN

Affiliation: Vion Pharmaceuticals

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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