医学
化疗
奥沙利铂
粘膜炎
全血细胞减少症
内科学
中性粒细胞减少症
伊立替康
养生
化疗方案
败血症
癌症
胃肠病学
肿瘤科
外科
结直肠癌
骨髓
作者
Beatriz Suarez Martinez-Falero,Roopinder Gillmore
出处
期刊:Case Reports
[BMJ]
日期:2014-04-03
卷期号:: bcr2013202040-bcr2013202040
被引量:2
标识
DOI:10.1136/bcr-2013-202040
摘要
A 71-year-old patient receiving combination chemotherapy (irinotecan, oxaliplatin and 5-fluorouracil (5-FU)) for metastatic pancreas cancer was admitted after her first cycle of chemotherapy with a severe and unexpectedly prolonged episode of neutropenic sepsis associated with pancytopenia and marked mucositis. Owing to the unusual picture, the patient was tested for mutations in the gene encoding the enzyme dihydropyrimidine dehydrogenase (DPD)—an enzyme involved in the metabolism of the chemotherapy drug 5-FU. The patient was found to be heterozygous for a mutation, DPD IVS14+1G>A, leading to the severe toxicity exhibited following this regimen caused by delayed metabolism of 5-FU. She was treated aggressively with supportive care and recovered from this episode. Importantly she was subsequently switched to an alternative chemotherapy regimen to treat her disease. She continues to maintain an excellent quality of life some 9 months after her initial diagnosis on third-line chemotherapy.
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