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AML Treatment in Untreated Adult Patients According to EORTC-GIMEMA Protocols AML8 and AML10
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.
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.
Age
15 - 61 years
Sex
ALL
Healthy Volunteers
No
Prof. Mozzana
Gallarate, Italy
Dr. De Blasio
Latina, Italy
Prof. Nalli
Lodi, Italy
Prof. Bordigon
Milan, Italy
Dr Miraglia
Naples, Italy
Dr. Mettivier
Naples, Italy
Dr.ssa Mastrullo
Naples, Italy
Prof. Pane
Naples, Italy
Prof. D'Arco
Nocera Inferiore, Italy
Dr Avanzi
Novara, Italy
Start Date
November 1, 1998
Primary Completion Date
June 1, 2018
Completion Date
July 1, 2018
Last Updated
November 17, 2017
Identification of appropriate therapies according to risks factors
PROCEDURE
Daunorubicine
DRUG
Transplant
PROCEDURE
Lead Sponsor
Gruppo Italiano Malattie EMatologiche dell'Adulto
NCT02158858
NCT00201240
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT00479232