Intensified Post Remission Therapy Containing PEG-Asparaginase
Acute Lymphoblastic Leukemia
About this trial
This is an interventional treatment trial for Acute Lymphoblastic Leukemia
Eligibility Criteria
Inclusion Criteria: Patients with previously untreated ALL subtypes L1 and L2. Patients with de novo Philadelphia (Ph)+ ALL (i.e. excluding those that are after blastic of CML) are eligible. However they will be referred to allogeneic hematopoietic stem cell transplantation and will continue on the study until they are ready to undergo the transplantation. At that time they will discontinue the study. Patients who are unable to undergo allogeneic transplantation will continue on the study. Presence of 25% or more of lymphoblasts in the bone marrow by FAB criteria, confirmed by TdT positivity or by flow cytometry with standard ALL markers. Patients may have received prior steroids. Age: 18 - 55 years Signed Informed Consent Exclusion Criteria: Patients with Burkitt's ALL (L3 subtype) or CML lymphoblastic crisis are not eligible (including CML patients who present with ALL blastic crisis). Psychological or emotional disorders which will make a valid informed consent impossible. Bilirubin >1.5 mg/dl, creatinine > 2.5 mg/dl Symptomatic congestive heart failure or unstable angina Pregnant or lactating females Known HIV positive status
Sites / Locations
- USC/Norris Comprehensive Cancer Center and Hospital
Arms of the Study
Arm 1
Experimental
Intensified Post-Remission: MTX/LV/PEG-Asparaginase
Daunorubicin 60 mg/m2 iv on days 1, 2, 3 Vincristine 1.4 mg/m2 iv on days 1, 8, 15, 22 Peg-Asparaginase 2000 U/m2 iv on day 15 Prednisone 60 mg/m2 mg po on days 1-28 MTX 12 mg IT on days 8 & 15