Advani Pooja P, Fakih Marwan G
Roswell Park Cancer Institute, Buffalo, NY 14203, USA.
Anticancer Res. 2011 Jan;31(1):335-8.
Neurological complications of both fluorouracil (5-FU) and its oral prodrug, capecitabine, have been described in the literature. This study reported the case of a 70-year-old female with metastatic adenocarcinoid of the rectum who developed hyperammonemic encephalopathy, following infusional 5-FU therapy, manifesting itself as intractable nausea, vomiting, confusion and disorientation. Interestingly, when the patient was rechallenged with the fluoropyrimidine analog, capecitabine, neither hyperammonemia nor symptom recurrence was observed. 5-FU is an integral component of effective anti-neoplastic treatment for metastatic colorectal cancer, but is often discontinued when neurotoxicity develops. This case highlighted the use of capecitabine as an alternative for patients who have demonstrated evidence of 5-FU-induced hyperammonemic encephalopathy. Re-challenging the patient with capecitabine, at a low daily dose intensity, accounted for the overall tolerability of the treatment, as demonstrated by normal ammonia levels and the lack of neurological symptoms.
文献中已描述了氟尿嘧啶(5-FU)及其口服前体药物卡培他滨的神经并发症。本研究报告了一例70岁女性直肠转移性类癌患者,在接受5-FU输注治疗后发生高氨血症性脑病,表现为顽固性恶心、呕吐、意识模糊和定向障碍。有趣的是,当患者再次接受氟嘧啶类似物卡培他滨治疗时,未观察到高氨血症或症状复发。5-FU是转移性结直肠癌有效抗肿瘤治疗的重要组成部分,但当发生神经毒性时通常会停药。该病例突出了卡培他滨可作为已证明有5-FU诱导的高氨血症性脑病证据的患者的替代药物。以低日剂量强度再次给予患者卡培他滨,氨水平正常且无神经症状,证明了该治疗的总体耐受性。