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Published on: September 18, 2013
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.
Purpose:
We used duration of hospitalization as a surrogate for cost and event-free survival as a measure of effectiveness to estimate the cost-effectiveness ratios of various treatment regimens on Children's Cancer Group trials for acute lymphoblastic leukemia.
Patients And Methods:
The analyses included 4,986 children (2 to 21 years of age) with newly diagnosed acute lymphoblastic leukemia enrolled onto risk-adjusted protocols between 1988 and 1995. Analyses were based on a model of 100 patients. The marginal cost-effectiveness ratio (hospital days per additional patient surviving event-free) was the difference in total duration of hospitalization divided by the difference in number of event-free survivors at 5 years for two regimens. Relapse-adjusted marginal cost of frontline therapy was the difference in total duration of hospitalization for frontline therapy plus relapse therapy divided by the difference in number of event-free survivors at 5 years on the frontline therapy for two regimens.
Results:
One or two delayed intensification (DI) phases, augmented therapy, and dexamethasone all improved outcome. Marginal cost-effectiveness of these regimens compared with the control regimens was 133 days per patient for DI, 117 days per patient for double DI, and 41 days per patient for augmented therapy. Dexamethasone resulted in 17 fewer days per patient. Relapse-adjusted marginal costs were 68 days per patient for DI and 52 days for double DI. Augmented therapy and dexamethasone-based therapy resulted in 16 and 82 fewer hospital days, respectively. The estimated cost-effectiveness for treating any first relapse was 250 days per patient.
Conclusion:
DI, double DI, augmented therapy, and dexamethasone-based therapy are cost-effective strategies compared with current treatment of first relapse.
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