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Completed

NCT Number: NCT01188174

Clofarabine/Ara-C Treatment Combined With Reduced-intensity Conditioning Allogeneic Stem Cell Transplantation for Acute Myeloid Leukemia in Primary Treatment Failure

The present trial will establish a prospective sequential Allogeneic Stem Cell Transplantation (allo-SCT) treatment combining both salvage chemotherapy and Reduced Intensity Conditioning (RIC) for primary treatment failure Acute Myeloid Leukemia (AML), to which future innovative strategies can be compared.

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Key information

Conditions

AML

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

CHU de Bordeaux, Bordeaux, France

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About this study

Primary Endpoint: To improve the 2 year overall survival in patients with primary treatment failure

  • Secondary Endpoints:
  • Feasibility of early transplantation within a multicenter trial
  • Leukemia-free survival (LFS) at 2 years from transplantation
  • Leukemia Response rate at day +30, +90 and 6 months
  • Cumulative incidence of relapse, death from leukemia, and non-relapse mortality (NRM)
  • Incidence and severity of acute and chronic Graft-versus-Host disease
  • Feasibility and safety of early discontinuation of immunosuppressive therapy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed diagnosis of AML in the status of primary induction failure (i.e. persistent leukemia after 2 courses of induction chemotherapy or persisting bone marrow hypoplasia fol-lowing induction chemotherapy +/-minimal residual disease)
  • Age: 18-55 years
  • Availability of an HLA identical family donor OR unrelated donor with matching in 10/10 alleles (HLA-A, B, C, DRB1, DQB1) or maximum of 1 allele or antigen mismatch OR family donor with maximum 1 allele mismatch.
  • Have adequate renal and hepatic functions as indicated by the following laboratory values:
  • Serum creatinine ≤1.0 mg/dL; if serum creatinine >1.0 mg/dL, then the estimated glomerular filtration rate (GFR) must be >60 mL/min/1.73 m² as calculated by the Modification of Diet in Renal Disease equation where Predicted GFR (ml/min/1.73 m2) = 186 x (Serum Creatinine)-1.154 x (age in years)-0.023 x (0.742 if patient is female)
  • Serum bilirubin ≤1.5 mg/dL × upper limit of normal (ULN)
  • Aspartate transaminase (AST)/alanine transaminase (ALT) ≤2.5 × ULN
  • Alkaline phosphatase ≤2.5 × ULN

Exclusion criteria

  • Documented chloroma
  • Patients having AML M3
  • Documented leukemic infiltration of CNS/cerebrospinal fluid
  • Karnofsky performance score below < 60%
  • Acute or chronic heart failure
  • HIV infection, chronic viral hepatitis
  • Severe neurological or psychiatric disorders
  • Any circumstances that preclude the use of the drugs used within the protocol
  • Prior allogeneic or autologous stem cell transplantation
  • > 3 courses of prior chemotherapy
  • Denied informed consent
  • Pregnancy or denied of effective contraceptive method

Treatment and study plan

Clofarabine

Drug

The present protocol aims to test the strategy of an early Reduced Intensity Conditioning (RIC) allo-SCT; in combination with a sequential preparative regimen for allo-SCT (Clofarabine, Intermediate dose Ara-C chemotherapy, followed by RIC with Cyclophosphamide, IV Busulfan and ATG; and delayed prophylactic infusion of donor lymphocytes (DLI) will be able to improve the outcome of patients with primary treatment failure AML.

Primary outcomes

  1. Evaluation of the survival rate at 2 years after transplantation

    Time frame: at 2 years after transplantation

Sponsors and collaborators

Lead sponsor

Nantes University Hospital

Other

Registry information

Acronym: setric

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Aug 25, 2010
Registry last updated
Dec 5, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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