Oncology Department, Hadassah-Hebrew University Medical Center, Ein Kerem, POB 12000, 91120 Jerusalem, Israel.
Int J Clin Oncol. 2010 Aug;15(4):420-2. doi: 10.1007/s10147-010-0050-0. Epub 2010 Mar 10.
We report a case of renal tubular acidosis (RTA) secondary to capecitabine, oxaliplatin, and cetuximab administration in a 63-year-old woman with liver metastasis from colon carcinoma who had partial treatment response. On day 5 posttreatment, she arrived to the emergency room with severe weakness, and blood tests demonstrated hypokalemia with metabolic acidosis. Urine potassium levels were elevated, and the transtubular potassium gradient (TTKG) was 6.6, consistent with hypokalemic RTA with associated Fanconi syndrome, which presented as hyperphosphaturia, uricaciduria, and loss of protein and sugar in the urine. She was treated with intravenously administered potassium and fluids. RTA is one type of nephrotoxicity induced by chemotherapy, and it is reversible in mild cases when appropriately treated. The mechanism of RTA induced by chemotherapy in cancer patients has not yet been clearly elucidated. Oncologists should therefore be aware of the potential for RTA to occur after capecitabine, oxaliplatin, and cetuximab treatment, especially in the context of other predisposing factors.
我们报告了一例由卡培他滨、奥沙利铂和西妥昔单抗联合治疗引起的肾性小管酸中毒(RTA)的病例。患者为一名 63 岁女性,患有结肠癌肝转移,治疗后部分缓解。在治疗后第 5 天,她因严重乏力到急诊就诊,血液检查显示低钾血症合并代谢性酸中毒。尿钾水平升高,肾小管钾梯度(TTKG)为 6.6,符合低钾性 RTA 伴发的范可尼综合征,表现为高磷尿症、尿酸尿症和尿中蛋白质和糖的丢失。她接受了静脉补钾和补液治疗。RTA 是化疗引起的一种肾毒性,在轻度病例中,适当治疗后是可逆的。癌症患者化疗引起的 RTA 的机制尚未明确。因此,肿瘤学家应该意识到卡培他滨、奥沙利铂和西妥昔单抗治疗后可能会发生 RTA,尤其是在存在其他诱发因素的情况下。