Literature DB >> 21627338

Iron-chelating therapies in a transfusion-dependent thalassaemia population in Thailand: a cost-effectiveness study.

Nantasit Luangasanatip1, Nathorn Chaiyakunapruk, Nilawan Upakdee, Peerapon Wong.   

Abstract

BACKGROUND AND
OBJECTIVE: β-Thalassaemia is a major public health problem in Thailand. Use of appropriate iron-chelating agents could prevent thalassaemia-related complications, which are costly to the healthcare system. This study aimed to evaluate the cost effectiveness of deferoxamine (DFO), deferiprone (DFP) and deferasirox (DFX) in Thai transfusion-dependent β-thalassaemia patients from the societal perspective.
METHODS: A Markov model was used to project the life-time costs and outcomes represented as quality-adjusted life-years (QALYs). Data on the clinical efficacy and safety of all therapeutic options were obtained from a systematic review and clinical trials. Transition probabilities were derived from published studies. Costs were obtained from the Thai Drug and Medical Supply Information Center, Thai national reimbursement rate information and other Thai literature sources. A discount rate of 3% was used. Incremental cost-effectiveness ratios (ICERs) were presented as year 2009 values. A base-case analysis was performed for thalassaemia patients requiring regular blood transfusion therapy, while a separate analysis was performed for patients requiring low (i.e. symptom-dependent, less frequent) blood transfusion therapy. A series of sensitivity analysis and cost-effectiveness acceptability curves were constructed.
RESULTS: Compared with DFO, using DFP was dominant with lifetime cost savings of $US91 117. Comparing DFX with DFO, the incremental cost was $US522 863 and incremental QALY was 5.77 with an ICER of $US90 648 per QALY. When compared with DFP, the ICER of DFX was $US106 445 per QALY. A cost-effectiveness analysis curve showed the probability of DFX being cost effective was 0% when compared with either DFO or DFP, based on the cost-effectiveness cut-off value of $US2902 per QALY. When compared with DFP, DFX was cost effective only if the DFX cost was as low as $US1.68 per 250 mg tablet. The results of the analysis in patients requiring low blood transfusion therapy were not different from those of the base-case analysis.
CONCLUSIONS: Our findings suggest that using DFP is cost saving when compared with conventional therapy, while using DFX is not cost effective compared with either DFO or DFP in Thai patients with transfusion-dependent β-thalassaemia. Policy-makers and clinicians may consider using such information in their decision-making process in Thailand.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21627338     DOI: 10.2165/11587120-000000000-00000

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  29 in total

Review 1.  Secondary iron overload.

Authors:  J P Kushner; J P Porter; N F Olivieri
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2001

2.  Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004.

Authors:  Paul Telfer; Pietro G Coen; Soteroula Christou; Michael Hadjigavriel; Anita Kolnakou; Evangelia Pangalou; Nicos Pavlides; Michael Psiloines; Krikor Simamonian; Georghios Skordos; Maria Sitarou; Michael Angastiniotis
Journal:  Haematologica       Date:  2006-09       Impact factor: 9.941

Review 3.  Oral deferiprone for iron chelation in people with thalassaemia.

Authors:  D J Roberts; S J Brunskill; C Doree; S Williams; J Howard; C J Hyde
Journal:  Cochrane Database Syst Rev       Date:  2007-07-18

4.  Cost effectiveness of once-daily oral chelation therapy with deferasirox versus infusional deferoxamine in transfusion-dependent thalassaemia patients: US healthcare system perspective.

Authors:  Thomas E Delea; Oleg Sofrygin; Simu K Thomas; Jean-Francois Baladi; Pradyumna D Phatak; Thomas D Coates
Journal:  Pharmacoeconomics       Date:  2007       Impact factor: 4.981

5.  Inherited haemoglobin disorders: an increasing global health problem.

Authors:  D J Weatherall; J B Clegg
Journal:  Bull World Health Organ       Date:  2001-10-24       Impact factor: 9.408

6.  A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia.

Authors:  Maria Domenica Cappellini; Alan Cohen; Antonio Piga; Mohamed Bejaoui; Silverio Perrotta; Leyla Agaoglu; Yesim Aydinok; Antonis Kattamis; Yurdanur Kilinc; John Porter; Marcello Capra; Renzo Galanello; Slaheddine Fattoum; Guillermo Drelichman; Carmelo Magnano; Monica Verissimo; Miranda Athanassiou-Metaxa; Patricia Giardina; Alexandra Kourakli-Symeonidis; Gritta Janka-Schaub; Thomas Coates; Christiane Vermylen; Nancy Olivieri; Isabelle Thuret; Herbert Opitz; Catherine Ressayre-Djaffer; Peter Marks; Daniele Alberti
Journal:  Blood       Date:  2005-12-13       Impact factor: 22.113

7.  Iron-chelation therapy with oral deferiprone in patients with thalassemia major.

Authors:  N F Olivieri; G M Brittenham; D Matsui; M Berkovitch; L M Blendis; R G Cameron; R A McClelland; P P Liu; D M Templeton; G Koren
Journal:  N Engl J Med       Date:  1995-04-06       Impact factor: 91.245

8.  Cardiac related death in thalassaemia major: time trend and risk factors in a large Greek Unit.

Authors:  Giorgos Chouliaras; Constantin T Yiannoutsos; Vasilios Berdoukas; Vassilios Ladis
Journal:  Eur J Haematol       Date:  2009-01-09       Impact factor: 2.997

9.  Cost-utility analysis of deferasirox compared to standard therapy with desferrioxamine for patients requiring iron chelation therapy in the United Kingdom.

Authors:  J Karnon; K Tolley; J Oyee; K Jewitt; D Ossa; R Akehurst
Journal:  Curr Med Res Opin       Date:  2008-04-24       Impact factor: 2.580

10.  Quality of life related to oral versus subcutaneous iron chelation: a time trade-off study.

Authors:  Richard H Osborne; Richard De Abreu Lourenço; Andrew Dalton; Jennifer Houltram; David Dowton; Douglas Edgar Joshua; Robert Lindeman; Phoebe Joy Ho
Journal:  Value Health       Date:  2007 Nov-Dec       Impact factor: 5.725

View more
  9 in total

1.  Cost-Utility Analysis of Three Iron Chelators Used in Monotherapy for the Treatment of Chronic Iron Overload in β-Thalassaemia Major Patients: An Italian Perspective.

Authors:  Alessia Pepe; Giuseppe Rossi; Anthony Bentley; Maria Caterina Putti; Ludovica Frizziero; Domenico Giuseppe D'Ascola; Liana Cuccia; Anna Spasiano; Aldo Filosa; Vincenzo Caruso; Aishah Hanif; Antonella Meloni
Journal:  Clin Drug Investig       Date:  2017-05       Impact factor: 2.859

2.  New developments and controversies in iron metabolism and iron chelation therapy.

Authors:  Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2016-03-26

Review 3.  World health dilemmas: Orphan and rare diseases, orphan drugs and orphan patients.

Authors:  Christina N Kontoghiorghe; Nicholas Andreou; Katerina Constantinou; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2014-09-26

4.  Dysregulation of iron metabolism in Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.

Authors:  Satoru Oshiro; Masaki S Morioka; Masataka Kikuchi
Journal:  Adv Pharmacol Sci       Date:  2011-10-12

Review 5.  Economic Evaluation of Chelation Regimens for β-Thalassemia Major: a Systematic Review.

Authors:  Jialian Li; Yong Lin; Xue Li; Jiayou Zhang
Journal:  Mediterr J Hematol Infect Dis       Date:  2019-07-01       Impact factor: 2.576

Review 6.  The History of Deferiprone (L1) and the Paradigm of the Complete Treatment of Iron Overload in Thalassaemia.

Authors:  George J Kontoghiorghes; Marios Kleanthous; Christina N Kontoghiorghe
Journal:  Mediterr J Hematol Infect Dis       Date:  2020-01-01       Impact factor: 2.576

7.  Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness study.

Authors:  Shaikha Alshamsi; Samer Hamidi; Hacer Ozgen Narci
Journal:  BMC Health Serv Res       Date:  2022-03-05       Impact factor: 2.655

8.  Cost-utility analysis of deferiprone for the treatment of β-thalassaemia patients with chronic iron overload: a UK perspective.

Authors:  Anthony Bentley; Samantha Gillard; Michael Spino; John Connelly; Fernando Tricta
Journal:  Pharmacoeconomics       Date:  2013-09       Impact factor: 4.981

9.  Cost-Utility Analysis of four Chelation Regimens for β-thalassemia Major: a Chinese Perspective.

Authors:  Jialian Li; Peng Wang; Xue Li; Qiaoyu Wang; Jiayou Zhang; Yong Lin
Journal:  Mediterr J Hematol Infect Dis       Date:  2020-05-01       Impact factor: 2.576

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.