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LAL-AR-N-2005:Study Treatment for Children High Risk Acute Lymphoblastic Leukemia

LAL-AR-N-2005: Study Treatment for Children High Risk Acute Lymphoblastic Leukemia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00526409
Acronym
LAL-AR-N-2005
Enrollment
40
Registered
2007-09-10
Start date
2005-06-30
Completion date
2014-10-31
Last updated
2014-10-28

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

Conditions

Acute Lymphoblastic Leukemia

Keywords

Acute Lymphoblastic Leukemia

Brief summary

The study objective is to improve the global results obtained with LAL-AR-93 study, reaching an event free survival between 60-70%. Identify patients with bad prognosis, with minimal residual disease,who can benefit of allogenic bone marrow transplantation

Detailed description

INDUCTION TREATMENT Systemic chemotherapy: PREDNISOLONE 60 mg/m2 /day, oral or i.v. x 21 days (1 to 22) 30 mg/m2 /day, oral or i.v. x 7 days (23 to 29) DAUNORUBICIN 30 mg/m2 , i.v. days 1,8,15 and 22 VINCRISTINE 1,5 mg/m2, i.v. days 1,8,15 and 22 L-ASPARAGINASE 10.000U/m2 i.m or i.v day 9,11,13,16,18,20,23,25 and 27 CYCLOPHOSPHAMIDE 500 mg/m2 i.v. days 1,2 and 29 Intrathecal chemotherapy: Days 1 and 22 according age: Age \<1 years 1-3 years \>3 years Methotrexate (MTX), mg 5 8 12 Ara-C, mg 16 20 30 Hydrocortisone,mg 10 10 20 Patients with \<10% blasts in M.O (day 14), and in complete response on week 5 or 6, and without MDR, start consolidation-intensification phase. Patients with \>10% blasts in MO day +14 or without CR after induction treatment, start consolidation-intensification phase and identifier a donor for a transplantation. CONSOLIDATION/INTENSIFICATION (C.I.) Two sequential cycles, alternating bloc I and bloc II BLOC I DEXAMETHASONE 10 mg/m2/d vo. days 1 to 5 and 5 mg/m2/d vo. days 6 and 7 VINCRISTINE 1.5 mg/m2/d, i.v. days 1 and 8 METHOTREXATE 5 g/m2 24 hours infusion + AF, day 1 ARA-C 1 g/m2/12 h, i.v., days 5 and 6 MERCAPTOPURINE 100 mg/m2/d, oral, days 1 to 5 CYCLOPHOSPHAMIDE 500 mg/m2 i.v. el day +8 INTRATHECAL CHEMOTHERAPY day 1. BLOC II DEXAMETHASONE 10 mg/m2/d, v o. days 1-5 and 5 mg/m2/d, v o. days 6 and 7 VINCRISTINE 1.5 mg/m2/d, days 1 and 8 METHOTREXATE 5 g/m2 24 h infusion + AF, day 1 ARA-C 1 g/m2 i.v/12 h, days 5 and 6 DAUNORUBICINE 30 mg/m2 i.v.day 1 L-ASPARAGINASE 20.000 u/m2/d, i.m. or i.v. day 7 INTRATHECAL CHEMOTHERAPY day 1 Patients with CR and MRD negative, follow chemotherapy. Patients with MDR \>0.01% after second cycle or considered previously MRD are candidates to allogenic transplantation after second cycle. REINDUCTION/INTENSIFICATION TREATMENT (R.I.) PREDNISOLONE 60 mg/m2/d, oral x 14 days (1-14) 30 mg/m2/d, oral x 7 days (15-22) VINCRISTINE 1.5 mg/m2, i.v. x 2 days 1 and 8 DAUNORUBICINE 30 mg/m2 i.v x 2 , days 1 and 8 CYCLOPHOSPHAMIDE 500 mg/m2 I.V. day 15 \----------------------------------------- METHOTREXATE 3 g/m2 /24 h infusion + AF day 29 MERCAPTOPURINE 50 mg/m2/d, oral, days 29-35 and 43-50 ARA-C 1 g/m2/12 h., i.v., days 43 and 44 INTRATHECAL CHEMOTHERAPY , days 1, 15, 29 and 43 MAINTENANACE TREATMENT (M1) Six cycles of: MERCAPTOPURINE 50 mg/m2/d, oral x 21 days (1-21) METHOTREXATE 20 mg/m2/d, i.m. /week x 3 (1,7,14) PREDNISOLONE 60 mg/m2/d, oral x 7 days (22-28) VINCRISTINE 1.5 mg/m2 i.v.day 22 ASPARAGINASE 20.000 u/m2 i.m. day 22 INTRATHECAL CHEMOTHERAPY day 22 MAINTENANCE TREATMENT (M2) Diary mercaptopurine and weekly methotrexate at previous doses, until complete 24 months.

Interventions

DRUGPrednisolone

Induction: 60 mg/m2/day, oral or i.v x 21 days and 30 mg/m2/day oral or iv x 7 days Reinduction-Intensification Treatment: 60 mg/m2/d x 14 days and 30 mg/m2/day oral x 7 days

DRUGDaunorubicin

Induction: 30 mg/m2, i.v, days 1, 8, 15, 22 Consolidation (Bloc II)30 mg/m2, i.v, day 1

DRUGVincristine

Induction: 1,5 mg/m2 iv, days 1, 8, 15, 22 Consolidation (Bloc I):1,5 mg/m2 iv, days 1, 8 Consolidation (Bloc II):1,5 mg/m2 iv, days 1, 8 Reinduction: 1,5 mg/m2 iv, days 1, 8 Maintenance:1,5 mg/m2 iv, day 22

Induction: 10.000 U/m2 im or iv, days 9,11,13,16,18,20,23,25,27 Consolidation (Bloc II): 20.000 U/m2 im or iv, day 7 Maintenance: 20.000 U/m2 im or iv, day 22

DRUGCyclophosphamide

Induction: 500 mg/m2 iv, days 1, 2, 29 Consolidation (Bloc I): 500 mg/m2 iv, day 8 Reinduction:500 mg/m2 iv, day 15

DRUGMethotrexate

Consolidation (Bloc I): 5 g/m2 24 hours infusion Consolidation (Bloc II): 5 g/m2 24 hours infusion Reinduction: 3 g/m2 24 hours infusion Maintenance: 20 mg/m2/d, IM/week x 3 (1, 7, 14)

Consolidation (Bloc I): 1 g/m2/12 h iv, days 5, 6 Consolidation (Bloc II): 1 g/m2/12 h iv, days 5, 6 Reinduction: 1 g/m2/12 h iv, days 43, 44

Sponsors

PETHEMA Foundation
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 16 Years
Healthy volunteers
No

Inclusion criteria

* High risk children with acute lymphoblastic leukemia

Exclusion criteria

* Mature B-ALL (FABL3) * Mixed forms of ALL * Patients with coronary disorders, valvular or hypertensive cardiopathy * Patients with chronic liver disorders * Chronic pulmonary disorders * Renal insufficiency * Neurologic disfunctions * ECOG 3 and 4

Design outcomes

Primary

MeasureTime frame
To improve the global results obtained in PETHEMA LAL-AR-93 study in terms of events free time2 years

Countries

Spain

Outcome results

None listed

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