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Completed

NCT Number: NCT01301820

Elderly Patients With Acute Myeloid Leukemia (AML), Maintenance Phase After Complete Remission (CR)

Phase II Multicentric Trial Open Label, Multicenter, randomized to evaluate the efficacy of a Maintenance Therapy in First Complete Remission After Induction for Elderly (≥ 60) Fit Patients With Poor Prognosis Acute Myeloid Leukemia (AML).

The disease-free survival (DFS) of the patients included in this study will be compared to the ones of the two previously reported groups of patients treated with the same LIA induction therapy

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Key information

Age range

60 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Mathilde HUNAULT BERGER

Angers, 49033, France

About this study

  • The primary objective of this study will be to improve the DFS with an alternate schema combining azacitidine and lenalidomide in elderly fit patients with previously untreated AML and with high risk cytogenetics or secondary AML, who achieved either a complete remission after an LIA induction therapy
  • The secondary objectives will be to determine the relapse incidence, overall survival, event free survival at 1 and 2 years of follow-up, toxicities of the treatment, incidence of infectious events.
  • To define a gene expression and promoter methylation signatures associated with CR and absence of relapse when patients received azacitidine and lenalidomide. Gene promoter methylation and gene expression profiling will be performed at diagnosis, at CR, and after 2 courses of azacitidine and lenalidomide in order to give insight within the mechanisms involved by the use of these 2 drugs and to identify new epigenetic prognostic markers.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Cytologically or histologically confirmed acute myeloid leukemia (AML) with :
  • At least 60 years of age and fit for intensive chemotherapy: PS <2 (ECOG)
  • Absence of significant co-morbidities
  • Less than 75 years* of age
  • LAM with high risk features (blasts > 20% in bone marrow)
  • Poor risk cytogenetics
  • Life expectancy > 1 month
  • Affiliated to social security regimen
  • No granulocytic sarcoma as sole site of disease
  • Able and willing to provide written and signed informed consent

Exclusion criteria

  • Total bilirubin > 2 times upper limit of normal
  • AST and ALT and/or alkaline phosphatase > 4 times upper limit of normal if not in relation with AML.
  • Factor V < 50% without DIC (Disseminated Intravascular Coagulation)
  • NYHA class III or IV congestive heart failure (Echo < 40%, LVEF < 50%),Unstable angina pectoris, Serious cardiac arrhythmia
  • Renal failure not related to AML: serum creatinin > 170 μmol/L or clearance of creatinin ≤ 50 mL/mn
  • Known HIV 1- HIV 2 positivity
  • Prior therapy with azacitidine or lenalidomide
  • Psychiatric illness or social situations that would preclude compliance with study requirements
  • Uncontrolled infection
  • Urgent chemotherapy for DIC, spontaneous tumoral lyse syndrome, leucostase without cytogentic results
  • Women who are pregnant or breastfeeding
  • Women who are unwilling or unable to use an acceptable contraceptive method to avoid pregnancy
  • Men who are unwilling or unable to use an acceptable method of birth control

Treatment and study plan

Azacitidine

Drug

azacitidine sc 75 mg/m²/d (d1- d7)

Other names: vidaza®

Lenalidomide

Drug

lenalidomide 10mg/d (d1- d21)

Other names: revlimid®

Primary outcomes

  1. DFS

    Time frame: 18 months

    The primary objective of this study will be to improve the DFS with an alternate schema combining azacitidine and lenalidomide in elderly fit patients with previously untreated AML and with high risk cytogenetics or secondary AML, who achieved either a complete remission after an LIA induction therapy.

Secondary outcomes

  1. relapse incidence OS EFS Infectious events

    Time frame: until death

    The secondary objectives will be to determine the relapse incidence, overall survival, event free survival at 1 and 2 years of follow-up, toxicities of the treatment, incidence of infectious events.

  2. gene expression and promoter methylation signatures associated with CR

    To define a gene expression and promoter methylation signatures associated with CR and absence of relapse when patients received azacitidine and lenalidomide. Gene promoter methylation and gene expression profiling will be performed at diagnosis, at CR, and after 2 courses of azacitidine and lenalidomide in order to give insight within the mechanisms involved by the use of these 2 drugs and to identify new epigenetic prognostic markers.

Sponsors and collaborators

Lead sponsor

French Innovative Leukemia Organisation

Other

Collaborators

  • Celgene Corporation

Registry information

Official study title

Phase II Multicentric Trial Maintenance Therapy With 6 Monthly Revlimid® Cycles Alternated With 6 Monthly Vidaza® Cycles in First CR After Induction LIA Chemotherapy for Elderly Fit Patients With Poor Prognosis Acute Myeloid Leukemia.

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Feb 23, 2011
Registry last updated
Mar 16, 2016

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

View the official ClinicalTrials.gov record (opens in a new tab)

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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