» Articles » PMID: 22955130

Cost-effectiveness of HLA-B*1502 Genotyping in Adult Patients with Newly Diagnosed Epilepsy in Singapore

Overview
Journal Neurology
Specialty Neurology
Date 2012 Sep 8
PMID 22955130
Citations 44
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Asians who carry the HLA-B*1502 allele have an elevated risk of developing Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) when treated with the antiepileptic drugs (AEDs) carbamazepine (CBZ) and phenytoin (PHT). With a focus on Singapore, this analysis identifies circumstances in which genotyping and targeted treatment with alternative AEDs that do not induce SJS/TEN is likely to be more cost-effective than 1) treatment with CBZ or PHT without genotyping or 2) providing a more expensive drug that does not induce SJS/TEN to all patients without genotyping.

Methods: A decision tree model was developed in TreeAge. The model takes into account costs of epilepsy treatments and genotyping, reductions in quality of life and increased costs resulting from SJS/TEN complications, the prevalence of the risk allele, the positive predictive value (PPV) of genotyping, life expectancy, and other factors.

Results: Compared with no genotyping and providing CBZ to all, genotyping results in an incremental cost-effectiveness ratio of $37,030/quality-adjusted life year (QALY) for Chinese patients, $7,930/QALY for Malays, and $136,630/QALY for Indians in Singapore.

Conclusions: Because of the different population allele frequencies of HLA-B*1502 among different ethnic groups, genotyping for HLA-B*1502 and providing alternate AEDs to those who test positive is cost-effective for Singaporean Chinese and Malays, but not for Singaporean Indians. Population frequency of HLA-B*1502, PPV, duration of treatment relative to life expectancy, and costs of alternative drugs are the key drivers influencing cost-effectiveness.

Citing Articles

NF1 mutation-driven neuronal hyperexcitability sets a threshold for tumorigenesis and therapeutic targeting of murine optic glioma.

Anastasaki C, Chatterjee J, Koleske J, Gao Y, Bozeman S, Kernan C Neuro Oncol. 2024; 26(8):1496-1508.

PMID: 38607967 PMC: 11300021. DOI: 10.1093/neuonc/noae054.


Frequencies of HLA-B alleles in Indonesian Malay Ethnic.

Yuliwulandari R, Prayuni K, Viyati K, Mahasirimongkol S, Wichukchinda N Heliyon. 2024; 10(5):e26713.

PMID: 38439829 PMC: 10909668. DOI: 10.1016/j.heliyon.2024.e26713.


Drug-induced Stevens Johnson syndrome and toxic epidermal necrolysis: Interpreting the systematic reviews on immunomodulatory therapies.

Thong B Asia Pac Allergy. 2023; 13(2):72-76.

PMID: 37388817 PMC: 10287110. DOI: 10.5415/apallergy.0000000000000101.


Pharmacogenomics: current status and future perspectives.

Pirmohamed M Nat Rev Genet. 2023; 24(6):350-362.

PMID: 36707729 DOI: 10.1038/s41576-022-00572-8.


Cost Effectiveness of Pharmacogenetic Testing for Drugs with Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines: A Systematic Review.

Morris S, Alsaidi A, Verbyla A, Cruz A, Macfarlane C, Bauer J Clin Pharmacol Ther. 2022; 112(6):1318-1328.

PMID: 36149409 PMC: 9828439. DOI: 10.1002/cpt.2754.