DaunoXome + Ara-C vs Daunorubicin + Ara-C in Elderly AML

Overall results in the treatment of middle aged adults acute myelogenous leukemia (AML) are substantially improved in the last decade, with complete remission (CR) rates established to values of 70 to 80per cent and also encouraging long-term outcome, especially in patients who can tolerate intensified post remissional treatment strategies. On the contrary, there has been little progress in the treatment of older patients. In these patients the response rate generally range between 40 and 60per cent, and overall survival at 2 years is often less than 10 per cent.

Usually, a combination of anthracyclines daunomycin DNR or doxorubicin and cytarabyne Ara-C has been utilized for the remission-induction treatment, with schedules similar to those utilized in younger cases, for patients eligible to intensive treatments. Variation of the dose of DNR has not brought any significant benefit. The EORTC HOVON randomized trial AML9 compared two drugs in induction for previously untreated patients. DNR versus Mithoxantrone (MTZ). MTZ induction therapy produces a slightly better CR rate than DNR-containing regimen (47per cent vs 38per cent, P equals 0.069), without any significant effect on remission duration and survival. The DFS probability between the two treatment arms was not different. The median DFS estimates were 39 weeks in both groups. The DFS rate at 5 years was 8per cent. Also the duration of survival was similar (p equals 0.23) in the two treatment groups. Median survival estimates were 36 weeks (DNR) and 39 weeks (MTZ). The percentage of patients still alive at 5 years were 6per cent and 9per cent respectively.

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Key information

Conditions

AML Elderly

Age range

61 year–75 year

Study type

Interventional

Phase

Phase 3

About this study

It can be stated that single agent DaunoXome seems associated with a level of anti-leukemic activity at least equivalent to the conventional drugs available. In addition, the safety profile of DaunoXome either as a single agent either as a combination with Ara-C seems improved with respect to the conventionally administered anthracyclines. Therefore, it seems warranted to further explore the anti-leukemic activity, the toxicity and the long term results of DaunoXome as a treatment for AML in association with Ara-C against the parent compound daunorubicin. In particular, we propose a study to evaluate standard 3+7 schedule versus the same schedule with DaunoXome instead of daunorubicine as front line treatment in AML patients older than 60 years. Patients achieving a CR will receive a consolidation cycle with the same drugs at the same doses. After consolidation, patients in CR will be randomized to receive a maintenance treatment with low-dose Ara-C plus Atra versus no treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Previously untreated AML (including AML after MDS) with > 20% marrow blasts (new WHO classification)
Age ≥ 61 <75 years
AML evoluted after MDS are eligible if not previously treated with antiblastic drugs.
Performance status ≥ 70 (Karnofsky) or ≤ 2 (WHO)
Signed informed consent from the patient

Exclusion criteria

Version 3.0 - february 2001 - CONFIDENTIAL 9

Patients already treated for their AML with other cytotoxic drugs (except no more than 7 days of Corticosteroids)
Acute promyelocitic leukemia (FAB M3 or M3v)
Blast crisis of chronic myeloid leukemia or leukemia supervening after other
myeloproliferative disease
Concomitant progressive malignant disease
Presence of meningeal disease
History of recent myocardial infarction (within previous 12 months), significant congestive heart failure, life threatening arrhythmia, or cardiovascular disease of Class II or greater according to the New York Heart Association Functional Classification (NYHAFC).
Abnormal cardiac ejection fraction (45% or less).
Abnormal hepatic function (ALAT/ASAT or bilirubin >3 N ).
Abnormal renal function (creatinine >3 N)
Active bacterial, fungal or viral infection as documented by positive cultures, radiological imaging, clinical signs, septic fever or septic shock symptoms.
Patients who recover from the infection could be eligible.
History of hypersensitivity to one of the liposomal constituents.
Severe pulmonary, neurological or psychiatric disease.
People unable to give informed consent.
Presence of any phychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow up schedule.
HIV positivity
Intercurrent organ damage or medical problems that would interfere with therapy.

Treatment and study plan

daunoxome

Drug

Daunorubicine

Drug

Primary outcomes

Efficacy and safety of DaunoXome in association with cytosine arabinoside in terms of reduction of induction deaths respect to standard "3+7" chemotherapy

Secondary outcomes

Efficacy, in terms of DFS, of maintenance therapy with low-dose of Ara-C plus ATRA versus no maintenance therapy

Sponsors and collaborators

Lead sponsor

Gruppo Italiano Malattie EMatologiche dell'Adulto

Other

Registry information

Official study title

DaunoXome (Liposomal Daunorubicin) Plus Ara-C Versus Daunorubicin Plus Ara-C in Elderly AML Patients.A Randomized Phase III Study.

Important dates

Study start: 2001
Primary completion: 2005
Study completion: 2005
First posted: Jan 9, 2008
Registry last updated: Jan 9, 2008

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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