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在一种新的DPYD基因变异背景下,怀疑卡培他滨诱发致命毒性。

Suspected capecitabine-induced fatal toxicity in the context of a new DPYD variant.

作者信息

Thet Phu Ngone, Khalid Taha, Ganderton Rosalind, Iveson Timothy

机构信息

Gastroenterology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK

Southampton General Hospital, Southampton, UK.

出版信息

BMJ Case Rep. 2025 Aug 31;18(8):e265589. doi: 10.1136/bcr-2025-265589.

Abstract

We present the case of a male in his early 70s who died after receiving adjuvant chemotherapy, probably due to an undiagnosed dihydropyrimidine dehydrogenase (DPYD) deficiency. Despite normal results from standard DPYD genotyping prior to treatment, he developed severe gastrointestinal toxicity that progressed to bowel ischaemia and ultimately death. This case underscores the potential limitations of current genotyping approaches, which may not detect rare or functionally significant DPYD variants. It also highlights the need for a cautious and comprehensive approach to fluoropyrimidine therapy, especially in patients who develop unexpected toxicity, while recognising that other contributing factors may be involved.

摘要

我们报告了一例70岁出头的男性病例,该患者在接受辅助化疗后死亡,可能是由于未诊断出的二氢嘧啶脱氢酶(DPYD)缺乏症。尽管在治疗前标准DPYD基因分型结果正常,但他仍出现了严重的胃肠道毒性,进展为肠道缺血并最终死亡。该病例强调了当前基因分型方法的潜在局限性,这些方法可能无法检测到罕见的或具有功能意义的DPYD变异。它还强调了对氟嘧啶治疗采取谨慎和全面方法的必要性,特别是在出现意外毒性的患者中,同时认识到可能涉及其他促成因素。

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