Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update

The variant allele HLA‐B*15:02 is strongly associated with greater risk of Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in patients treated with carbamazepine or oxcarbazepine. The variant allele HLA‐A*31:01 is associated with greater risk of maculopapular exanthema, drug reac...

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Veröffentlicht in:Clinical pharmacology and therapeutics 2018-04, Vol.103 (4), p.574-581
Hauptverfasser: Phillips, Elizabeth J., Sukasem, Chonlaphat, Whirl‐Carrillo, Michelle, Müller, Daniel J., Dunnenberger, Henry M., Chantratita, Wasun, Goldspiel, Barry, Chen, Yuan‐Tsong, Carleton, Bruce C., George, Alfred L., Mushiroda, Taisei, Klein, Teri, Gammal, Roseann S., Pirmohamed, Munir
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Sprache:eng
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Zusammenfassung:The variant allele HLA‐B*15:02 is strongly associated with greater risk of Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in patients treated with carbamazepine or oxcarbazepine. The variant allele HLA‐A*31:01 is associated with greater risk of maculopapular exanthema, drug reaction with eosinophilia and systemic symptoms, and SJS/TEN in patients treated with carbamazepine. We summarize evidence from the published literature supporting these associations and provide recommendations for carbamazepine and oxcarbazepine use based on HLA genotypes.
ISSN:0009-9236
1532-6535
DOI:10.1002/cpt.1004