Toxicity and efficacy of intensive chemotherapy for children with acute lymphoblastic leukemia (ALL) after first bone marrow or extramedullary relapse

Pediatr Blood Cancer. 2004 Oct;43(5):571-9. doi: 10.1002/pbc.20128.

Abstract

Background: Approximately 25% of children newly diagnosed with acute lymphoblastic leukemia (ALL) will eventually experience leukemic relapse, with bone marrow being the most common site of recurrence. The ability to achieve a durable second remission is complicated by toxicity and resistant disease. We report a novel combination of chemotherapy for relapsed pediatric ALL.

Procedure: Thirty pediatric patients with relapsed medullary (n = 18) and extra-medullary (n = 12) ALL were enrolled at three pediatric institutions. Following receipt of induction and the first Block A and Block B of intensification, each patient was evaluated for toxicity, efficacy in achieving remission, and long-term survival. Additionally, minimal residual disease (MRD) detection by multidimensional flow cytometry (MDF) was performed.

Results: During induction, the major non-hematopoeitic toxicities were mucositis (30% of patients) and bacteremia (50% of patients). Two patients (7%) died of toxicity during induction. Toxicity during intensification Block 1A and 1B was markedly reduced. Eight-nine percent of patients with marrow disease achieved a remission following induction and intensification. The event-free survival (EFS) for all patients at 2 and 4 years were 60% (95% CI: 42-78%) and 49% (95% CI: 30-68%), respectively.

Conclusions: This regimen for patients with relapsed ALL was successful in achieving a second remission for the majority of patients with acceptable toxicity.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Asparaginase / administration & dosage
  • Bacteremia / chemically induced
  • Bone Marrow Neoplasms / drug therapy*
  • Bone Marrow Neoplasms / pathology*
  • Child
  • Child, Preschool
  • Cytarabine / administration & dosage
  • Dexamethasone / administration & dosage
  • Etoposide / administration & dosage
  • Female
  • Flow Cytometry
  • Humans
  • Idarubicin / administration & dosage
  • Ifosfamide / administration & dosage
  • Infant
  • Infusions, Intravenous
  • Leucovorin / administration & dosage
  • Male
  • Mesna / administration & dosage
  • Methotrexate / administration & dosage
  • Mouth Mucosa / pathology
  • Polyethylene Glycols / administration & dosage
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Recurrence
  • Stomatitis / chemically induced
  • Thioguanine / administration & dosage
  • Treatment Outcome
  • Vincristine / administration & dosage

Substances

  • Cytarabine
  • Polyethylene Glycols
  • Vincristine
  • Etoposide
  • pegaspargase
  • Dexamethasone
  • Asparaginase
  • Thioguanine
  • Mesna
  • Leucovorin
  • Ifosfamide
  • Methotrexate
  • Idarubicin