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PETHEMA LAL-RI/96: Treatment for Patients With Standard Risk Acute Lymphoblastic Leukemia

PETHEMA LAL-RI/96: Treatment for Patients With Standard Risk Acute Lymphoblastic Leukemia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00494897
Enrollment
374
Registered
2007-07-02
Start date
1996-06-30
Completion date
2007-12-31
Last updated
2009-05-19

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

Conditions

Acute Lymphoblastic Leukemia

Brief summary

The objective of current protocol is try improve the results of chemotherapy treatment in patients with ALL wich is not indicated the peripheral stem cell transplant in first remission, with an intensive consolidation follow by re-inductions.

Detailed description

Induction therapy: Patients with standard risk receive vincristine (1,5 mg/m2)IV on days 1, 8, 15 and 22;daunorubicin (30 mg/m2)IV on days 1, 8, 15 and 22; oral or IV prednisone 60 mg/m2/day, days 1 to 27 and 30 mg/m2/day, days 28 to 35;asparaginase 10.000 UI/m2 IM or IV, days 10 to 12, 17 to 19 and 24 to 26;cyclophosphamide (500 mg/m2)IV days 1, 2 and 29; methotrexate, cytosine arabinoside and hydrocortisone, days 1 to 22. Patients older than 55 years are not treated with asparaginase and cyclophosphamide. Consolidation therapy (1): Standard risk: Mercaptopurine 50 mg/m2, PO, days 1 to 7, 28-35 and 56-63; methotrexate (3g/m2)IV/24 hours, day 1, 28 and 56; VM-26 (150 mg/m2)/12 hours, IV, days 14 and 42; ARA-C (500 mg/m2)/12 hours, IV days 14-15 and 42-43; intrathecally treatment, days 1, 28 and 56. Patients over 50 years: Mercaptopurine (50 mg/m2), PO, days 1 to 7, 28-35 and 56-63;methotrexate (1,5 g/m2) IV/24 hours, day 1, 28 and 56; VM-26 (150 mg/m2)/12 hours, IV days 14 and 42; ARA-C (500 mg/m2)/12 hours, IV days 14-15 and 42-43; intrathecally treatment, days 1, 28 and 56. Consolidation therapy (2)/Reinduction: one cycle similar to induction. It starts one week after last dose of mercaptopurine.Dexamethasone 10 mg/m2/day,PO or IV, days 1-14 and 5 mg/m2/day, PO or IV days 15-21; VCR: 1,5 mg/m2 IV, days 1, 8 and 15; Daunorubicin 30 mg/m2 IV, days 1, 2, 8 and 9; cyclophosphamide 600 mg/m2/day IV, days 1 and 15; Asparaginase: 10.000 UI/m2 IM or IV, days 1-3 and 15-17;intrathecally treatment days 1 and 15 Maintenance therapy 1:administration of continuous chemotherapy (mercaptopurine and methotrexate) and reinductions until one year from diagnosis. * Continuous chemotherapy: * MP 50 mg/m2/day PO * MTX 20 mg/m2/week IM * Reinductions * VCR: 1,5 mg/m2 IV, day 1. * PDN: 60 mg/m2/day, IV or PO days 1 to 7 * L-ASA: 20.000 UI/m2, IM or IV day 1. * Intrathecally day 1 Seven cycles, weeks 25, 29, 33, 37, 41, 45 and 49. Maintenance therapy 2:administration of continuous chemotherapy (mercaptopurine and methotrexate) while second year from diagnosis (weeks 53 to 104). * MP 50 mg/m2/day, PO * MTX 20 mg/m2/week, IM.

Interventions

DRUGAsparaginase
DRUGCyclophosphamide
DRUGCytarabine
DRUGDaunorubicin
DRUGMercaptopurine
DRUGPrednisone
DRUGVincristine
DRUGMethotrexate
PROCEDUREIntrathecally treatment

Sponsors

PETHEMA Foundation
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Adults (over 15 years) with ALL standard risk no prior antiblastic chemotherapy

Exclusion criteria

* Mature B-ALL (FABL3) or with cytogenetic ALL Burkitt-like alterations (t\[8;14\], t\[2;8\], t\[8;22\]) * Mixed forms of ALL * Acute Leukemia no differentiate * Patients with coronary disorders, valvular or hypertensive cardiopathy * Patients with chronic liver disorders * Chronic pulmonary disorders * Renal insufficiency * Neurologic disfunctions * ECOG 3 and 4 * No signed consent form

Design outcomes

Primary

MeasureTime frame
Efficacy of treatment in adults with standard risk acute lymphoblastic leukemia2 years

Secondary

MeasureTime frame
Demonstrate that in this group of patients, the CNS relapse is not frequently and is not necessary cranial radiotherapy2 years
To evaluate the treatment tolerance1 year

Countries

Spain

Outcome results

None listed

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