[Cost-effectiveness analysis in the treatment of hematologic malignancies].

Chihiro Yamamoto
Author Information
  1. Chihiro Yamamoto: Division of Hematology, Department of Medicine, Jichi Medical University.

Abstract

Recent advancements in treatment have improved the prognosis of hematologic malignancies. However, the increasing cost of therapeutic drugs has become an urgent issue. Cost-effectiveness analysis is performed using the incremental cost-effective ratio (ICER), a value calculated by dividing the incremental cost by the incremental quality-adjusted life year (QALY). The ICER must be compared with the willingness-to-pay (WTP) threshold, which differs between countries. Since the analysis should be made over a long time horizon, it is necessary to model and extrapolate the long-term outcomes of clinical trials to calculate cumulative costs and QALYs. This article discusses several approaches to cost-effectiveness analysis for chronic myelogenous leukemia, multiple myeloma, and CAR-T therapy. As even expensive treatments could be cost-effective if they provide long treatment-free survival, it is essential to judge cost-effectiveness by an appropriate method, rather than price alone.

Keywords

MeSH Term

Humans
Cost-Benefit Analysis
Hematologic Neoplasms
Quality-Adjusted Life Years
Cost-Effectiveness Analysis

Word Cloud

Created with Highcharts 10.0.0analysisincrementaltreatmenthematologiccostCost-effectivenesscost-effectiveICERlongcost-effectivenessleukemiamyelomatherapyRecentadvancementsimprovedprognosismalignanciesHoweverincreasingtherapeuticdrugsbecomeurgentissueperformedusingratiovaluecalculateddividingquality-adjustedlifeyearQALYmustcomparedwillingness-to-payWTPthresholddifferscountriesSincemadetimehorizonnecessarymodelextrapolatelong-termoutcomesclinicaltrialscalculatecumulativecostsQALYsarticlediscussesseveralapproacheschronicmyelogenousmultipleCAR-Tevenexpensivetreatmentsprovidetreatment-freesurvivalessentialjudgeappropriatemethodratherpricealone[Cost-effectivenessmalignancies]ChimericantigenreceptorT-cellChronicmyeloidMultiple

Similar Articles

Cited By

No available data.