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Adult ALL Treatment at Diagnosis

GIMEMA Guidelines for the Treatment of Adult ALL Affected Patients at Diagnosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00537550
Acronym
LAL2000
Enrollment
Unknown
Registered
2007-10-01
Start date
2000-07-31
Completion date
2006-06-30
Last updated
2007-10-01

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

Conditions

Leukemia, Lymphocytic, Acute

Keywords

ALL, Adult

Brief summary

The present study has been designed to give participating centers the possibility of better understanding the diagnostic and prognostic factors of ALL patients.

Interventions

DRUGVincristine

Steroids pre-treatment

DRUGVincristin, Daunorubicine, Asparaginase, Methotrexate

Induction therapy

Sponsors

Gruppo Italiano Malattie EMatologiche dell'Adulto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of acute lymphoblastic leukemia (ALL) * Negative myeloperoxidase stain * Phenotype T (ALL-T) and B(ALL-B)

Exclusion criteria

* Creatinine \> 2.5mg/dL after adequate hydratation * LVEF \<50% * Presence of documented infections not responding to antibiotic and/or antifungal therapy * Presence of concomitant malignant diseases * Absence of any psychological condition that does not allow to intake high doses of cortisone * Patients who have received any antineoplastic chemiotherapy for more than 5 days * Patients who have received any steroids for more than 10 days

Countries

Italy

Outcome results

None listed

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