Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT, USA.
J Oncol Pharm Pract. 2021 Jan;27(1):26-32. doi: 10.1177/1078155220908946. Epub 2020 Mar 12.
High-dose methotrexate is a cytotoxic agent used to treat several malignancies. Urine alkalinization with sodium bicarbonate and hyperhydration are given with methotrexate to prevent drug precipitation in the kidneys. Due to a nationwide intravenous sodium bicarbonate shortage, an enteral-based urine alkalinization protocol was instituted. This study compared outcomes and adverse effects between the previously used intravenous and newly implemented enteral protocols.
Single center retrospective cohort study comparing parenteral and enteral urine alkalinization for patients that received methotrexate doses ≥ 500 mg/m between 1 April 2016 and 1 October 2018. The primary endpoint was time to methotrexate clearance. Secondary outcomes included length of stay, time to administration of methotrexate, amount of sodium bicarbonate utilized, toxicities of methotrexate, and protocol-associated adverse effects.
There were 67 patients included in the study for a total of 195 infusions. The average time to methotrexate clearance between the two cohorts was similar (parenteral 88 h vs. enteral 98 h = 0.06). Likewise, length of stay was not different between the two cohorts ( = ns). The enteral cohort methotrexate's doses were initiated faster and received significantly less intravenous sodium bicarbonate when compared to the parenteral cohort ( = 0.04). Rates of acute kidney injury, neutropenia, hepatotoxicity, and mucositis were similar between the two groups. There were higher rates of diarrhea and low serum bicarbonate values in the enteral cohort.
This study supports the ability to conserve intravenous sodium bicarbonate by using an enteral-based urine alkalization regimen for HD methotrexate, with no difference in outcomes or toxicity.
大剂量甲氨蝶呤是一种细胞毒性药物,用于治疗多种恶性肿瘤。在用甲氨蝶呤治疗时,通过给予碳酸氢钠碱化尿液和充分水化,以防止药物在肾脏中沉淀。由于全国静脉内碳酸氢钠短缺,因此制定了基于肠内的尿液碱化方案。本研究比较了先前使用的静脉内和新实施的肠内方案的结果和不良反应。
单中心回顾性队列研究,比较了 2016 年 4 月 1 日至 2018 年 10 月 1 日期间接受甲氨蝶呤剂量≥500mg/m2的患者使用肠外和肠内尿液碱化的情况。主要终点是甲氨蝶呤清除时间。次要结局包括住院时间、甲氨蝶呤给药时间、碳酸氢钠用量、甲氨蝶呤毒性以及与方案相关的不良反应。
共有 67 例患者入组,共 195 例输液。两组之间甲氨蝶呤清除时间相似(肠外 88 小时 vs. 肠内 98 小时=0.06)。同样,两组的住院时间无差异(=ns)。与肠外组相比,肠内组的甲氨蝶呤剂量更快开始,且静脉内碳酸氢钠用量明显减少(=0.04)。两组的急性肾损伤、中性粒细胞减少、肝毒性和黏膜炎发生率相似。肠内组腹泻和血清碳酸氢盐水平较低的发生率较高。
本研究支持通过使用基于肠内的尿液碱化方案来节省静脉内碳酸氢钠,而不会对结果或毒性产生影响。