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

Primary Purpose

Acute Lymphoblastic Leukemia

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Prednisolone
Daunorubicin
Vincristine
L-Asparaginase
Cyclophosphamide
Methotrexate
Cytosine Arabinoside
Sponsored by
PETHEMA Foundation
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Lymphoblastic Leukemia focused on measuring Acute Lymphoblastic Leukemia

Eligibility Criteria

undefined - 16 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hospital materno Infantil vall d'Hebrón
  • Hospital Niño Jesús
  • Hospital Virgen de la Arrixaca
  • Hospital Infantil Carlos Haya

Outcomes

Primary Outcome Measures

To improve the global results obtained in PETHEMA LAL-AR-93 study in terms of events free time

Secondary Outcome Measures

Full Information

First Posted
September 6, 2007
Last Updated
October 27, 2014
Sponsor
PETHEMA Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00526409
Brief Title
LAL-AR-N-2005:Study Treatment for Children High Risk Acute Lymphoblastic Leukemia
Acronym
LAL-AR-N-2005
Official Title
LAL-AR-N-2005: Study Treatment for Children High Risk Acute Lymphoblastic Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
PETHEMA Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia
Keywords
Acute Lymphoblastic Leukemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Prednisolone
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Daunorubicin
Intervention Description
Induction: 30 mg/m2, i.v, days 1, 8, 15, 22 Consolidation (Bloc II)30 mg/m2, i.v, day 1
Intervention Type
Drug
Intervention Name(s)
Vincristine
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
L-Asparaginase
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Methotrexate
Intervention Description
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)
Intervention Type
Drug
Intervention Name(s)
Cytosine Arabinoside
Intervention Description
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
Primary Outcome Measure Information:
Title
To improve the global results obtained in PETHEMA LAL-AR-93 study in terms of events free time
Time Frame
2 years

10. Eligibility

Sex
All
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bastida Pilar, Dr
Organizational Affiliation
Hospital Universitari Materno-Infantil Vall d'Hebron
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ribera Josep Mª, Dr
Organizational Affiliation
Germans Trias i Pujol Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital materno Infantil vall d'Hebrón
City
Barcelona
Country
Spain
Facility Name
Hospital Niño Jesús
City
Madrid
Country
Spain
Facility Name
Hospital Virgen de la Arrixaca
City
Murcia
Country
Spain
Facility Name
Hospital Infantil Carlos Haya
City
Málaga
Country
Spain

12. IPD Sharing Statement

Links:
URL
http://www.aehh.org
Description
Spanish association of Haematology

Learn more about this trial

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

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