Duration of hospitalization as a measure of cost on Children's Cancer Group acute lymphoblastic leukemia studies

P S Gaynon1, B C Bostrom, R J Hutchinson

  • 1Department of Pediatric Hematology-Oncology, Childrens Hospital, Los Angeles, CA, USA.

Insights

Delayed intensification (DI) and augmented therapy improve outcomes in childhood acute lymphoblastic leukemia (ALL). These cost-effective strategies reduce hospitalizations compared to first relapse treatment.

Area of Science:

  • Pediatric Oncology
  • Health Economics
  • Clinical Trial Analysis

Background:

  • Acute lymphoblastic leukemia (ALL) is a significant pediatric cancer.
  • Optimizing treatment effectiveness and cost is crucial for improving patient outcomes.
  • Previous studies have evaluated various treatment regimens for ALL.

Purpose of the Study:

  • To estimate the cost-effectiveness ratios of different treatment regimens for childhood ALL.
  • To utilize hospitalization duration as a surrogate for cost and event-free survival for effectiveness.
  • To compare novel strategies against current treatments for first relapse.

Main Methods:

  • Analysis of 4,986 children (2-21 years) with newly diagnosed ALL from Children's Cancer Group trials (1988-1995).
  • Modeling based on 100 patients to calculate marginal cost-effectiveness ratios (hospital days per event-free survivor).
  • Inclusion of relapse-adjusted marginal costs for frontline therapies.

Main Results:

  • Delayed intensification (DI), double DI, augmented therapy, and dexamethasone improved outcomes.
  • Marginal cost-effectiveness ranged from 41 days/patient (augmented therapy) to 133 days/patient (DI).
  • Relapse-adjusted marginal costs were lower for DI and double DI; augmented and dexamethasone therapies reduced hospital days significantly.

Conclusions:

  • Delayed intensification (DI), augmented therapy, and dexamethasone-based regimens are cost-effective.
  • These strategies demonstrate improved outcomes and reduced hospitalizations compared to current first relapse treatment.
  • The findings support the integration of these enhanced regimens in pediatric ALL treatment protocols.
Abstract