Trial Search Results

Low-Dose or High-Dose Vincristine and Combination Chemotherapy in Treating Young Patients With Relapsed B-Cell Acute Lymphoblastic Leukemia

This randomized phase III trial is studying low-dose vincristine to see how well it works compared with high-dose vincristine when given together with different combination chemotherapy regimens in treating young patients with intermediate-risk relapsed B-cell acute lymphoblastic leukemia. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) and giving the drugs in different ways and different doses may kill more cancer cells..

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Children's Oncology Group

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Drug: vincristine sulfate
  • Drug: prednisone
  • Drug: doxorubicin hydrochloride
  • Drug: pegaspargase
  • Drug: cytarabine
  • Drug: methotrexate
  • Drug: dexamethasone
  • Drug: etoposide
  • Drug: cyclophosphamide
  • Drug: leucovorin calcium
  • Biological: filgrastim
  • Drug: asparaginase
  • Drug: mercaptopurine

Phase:

Phase 3

Eligibility


Inclusion Criteria:

   - Diagnosis of acute lymphoblastic leukemia (ALL)

      - Bone marrow with > 25% L1 or L2 lymphoblasts (M3 marrow)

         - Patients with > 25% L3 marrow lymphoblasts and/or evidence of c-myc
         translocation are not eligible (considered Burkitt's or mature B-cell
         leukemia)

   - Intermediate-risk relapsed disease, meeting 1 of the following criteria:

      - Bone marrow relapse ≥ 36 months after initial diagnosis (defined as M3 marrow
      after previous remission from ALL)

      - Combined bone marrow and extramedullary (CNS* and/or testicular**) relapse ≥ 36
      months after initial diagnosis

      - Isolated extramedullary (CNS* and/or testicular**) relapse < 18 months after
      initial diagnosis

   - The following subtypes are not allowed:

      - T-lineage ALL

      - Mature B-cell (Burkitt's) leukemia (defined as L3 morphology and/or evidence of
      c-myc translocation)

      - Philadelphia-chromosome positive disease

   - No Down syndrome (trisomy 21)

   - Shortening fraction >= 27% by echocardiogram OR ejection fraction >= 50% by
   radionuclide angiogram

   - Bilirubin < 3.0 mg/dL

   - Not pregnant

   - Fertile patients must use effective contraception

   - No history of peripheral neuropathy >= grade 3 within the past month

   - No toxicity (i.e. peripheral neuropathy) >= grade 3 attributable to vincristine within
   the past month

   - At least 5 days since prior intrathecal chemotherapy

   - No prior hematopoietic stem cell or marrow transplantation

   - No prior cranial radiotherapy > 1200 cGy (for patients with CNS relapse)

   - No concurrent stem cell transplant

   - No concurrent alternative therapy

   - No concurrent itraconazole in patients receiving vincristine

   - No concurrent intensity-modulated radiotherapy

Ages Eligible for Study

1 Year - 29 Years

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Nadeem Mukhtar
6504978815
Not Recruiting