Literature DB >> 33305610

Case report: severe toxicity in an African-American patient receiving FOLFOX carrying uncommon allelic variants in DPYD.

Tristan M Sissung1, Lisa Cordes2, Cody J Peer1, Shruti Gandhy2, Jason Redman2, Julius Strauss3, William D Figg1,2.   

Abstract

Cancers of the colon are commonly treated with fluoropyrimidines, which often cause severe toxicities in patients with certain variants in DPYD. Y186C (rs115232898) and a variant in the 3' untranslated region (rs12132152) are uncommon alleles previously observed in African-Americans. An African-American female underwent 5-fluorouracil-based therapy (400 mg/m2 bolus, 1200 mg/m2/day over 46 h). The patient experienced severe pancytopenia after the first cycle. After 5-fluorouracil (5-FU) dose reduction (600 mg/m2/day), the steady-state 5-FU plasma concentration became 474 ng/ml (range 301-619 ng/ml) and increased following a subsequence dose increase (800 mg/m2/day; 1248 ng/ml). After a 1000 mg/m2/day dose resulted in myelosuppression, 5-FU was again de-escalated for the remaining cycles (600 mg/m2). The observed complications are likely a function of uncommon genetic variants that affect DPYD metabolism.

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Year:  2020        PMID: 33305610      PMCID: PMC7831885          DOI: 10.2217/pgs-2020-0120

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  14 in total

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10.  A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity.

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Journal:  Clin Pharmacol Ther       Date:  2013-04-03       Impact factor: 6.875

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