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AML Treatment in Untreated Adult Patients

AML Treatment in Untreated Adult Patients According to EORTC-GIMEMA Protocols AML8 and AML10

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00449319
Acronym
LAM99P
Enrollment
Unknown
Registered
2007-03-20
Start date
1998-11-30
Completion date
2018-07-31
Last updated
2017-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Myelocytic, Acute

Keywords

AML, adult, Hydroxyurea, Transplant, Toevaluate biological characteristics at diagnosis., To identify genetic alterations with prognostic relevance., To follow up cases monitoring minimal disease during remission., To evaluate pretreatment therapy in terms of response rate and toxicity., Disease free survival., Overal survival.

Brief summary

The present therapy intends to be an homogeneous treatment for AML patients based on a pretreatment with hydroxiurea plus an induction therapy with the standard arm with Daunorubicine as according to EORTC-GIMEMA AML10 study. The post-remissional treatment is based on transplant with HLA compatible donor is foreseen for all patients and autologous transplant for those without HLA compatible donor available.

Detailed description

GIMEMA treatment for adult (15-60 yrs) AML patients included a 3-drug induction cycle with DNR (50 mg/m2 d 1, 3, 5), cytarabine (100 mg/m2 d1-10), etoposide (100 mg/m2 d1-5) followed by an intensive consolidation with cytarabine (500 mg/m2/q12 hrs d1-d6) and the same anthracycline as in induction on d 4-6. Following consolidation, eligible pts (age \<45 or 55 yrs) with a HLA compatible sibling had to be allografted, the others, had to be autografted with autologous peripheral stem cell (PSC) collected during recovery from consolidation. BM and PB samples at diagnosis were centralized according to a national GIMEMA original study planned with the aim to accurately evaluate biological characteristics at diagnosis and to identify genetic alterations with prognostic relevance and to follow up cases monitoring minimal disease during remission. To allow the adequate collection and sending of samples before starting intensive chemotherapy, all patients received a 5-day pretreatment consisting of hydroxiurea (HU) at the dosage of 2 g/m2/day, also effective for debulkying of disease.

Interventions

PROCEDUREIdentification of appropriate therapies according to risks factors
PROCEDURETransplant

Sponsors

Gruppo Italiano Malattie EMatologiche dell'Adulto
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 61 Years
Healthy volunteers
No

Inclusion criteria

* AML de novo with bone marrow blasts \<=30% * Performance status: 0-3 * FAB subtype: all except M3 * Written informed consent

Exclusion criteria

* age \<15 years and \>= 61 years * pretreated AML with chemiotherapy (except Idrossiurea) or radiotherapy or corticosteroids for more than 7 days. * diagnosis of acute promyelocitic leukemia (M3) * Performance status = 4 * Uncontrolled infection

Countries

Italy

Contacts

Primary ContactMarco VIGNETTI, Dr
m.vignetti@gimema.it+39 06 441639831
Backup ContactPaola FAZI, Dr.
p.fazi@gimema.it+39 06 441639830

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026