Flombaum Carlos D, Liu Dazhi, Yan Shirley Qiong, Chan Amelia, Mathew Sherry, Meyers Paul A, Glezerman Ilya G, Muthukumar Thangamani
Renal Division, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Division of Nephrology and Hypertension, Department of Medicine, Weill Cornell Medical College, New York, New York.
Pharmacotherapy. 2018 Jul;38(7):714-724. doi: 10.1002/phar.2145. Epub 2018 Jun 27.
Acute kidney injury complicating high-dose methotrexate (HDMTX) therapy increases the risk for severe mucositis, myelosuppression, and death. It is unclear whether high-dose leucovorin and supportive therapy without the use of glucarpidase can reduce toxicity from HDMTX.
The charts of all patients at Memorial Sloan Kettering Cancer Center whose methotrexate (MTX) drug levels at 48 or 72 hours after administration were 10 times or more the toxic level were reviewed between January 2000 and December 2011.
Eighty-eight patients (median age 51 years, range 9-90 years) who received 100 courses of HDMTX were identified. Serum creatinine increased by 2-fold from baseline (median, range 1- to 10-fold), but all patients recovered kidney function. Serum levels of MTX were 69 μmol/L (median, range 2.2-400), 6.9 μmol/L (1.3-64), and 2.0 μmol/L (0.05-26) at 24, 48, and 72 hours, respectively, after administration. A statistically significant correlation existed between MTX levels at 48, 72, 96, and 120 hours after administration but not between 24 and 72 hours or subsequent time points. High-dose leucovorin was given in 81% of courses in accordance with institutional protocols in most cases. Myelosuppression was present in 42%; grade III or higher neutropenia in 29%, and thrombocytopenia in 25%. Infectious complications, oral mucositis, and diarrhea occurred in 21%, 17%, and 6% of patients, respectively. Five deaths occurred, none directly attributed to complications from MTX administration. Seven additional patients received glucarpidase at the discretion of a treating physician during the study period, and results are reported separately.
Patients who had 100 episodes of HDMTX-associated acute kidney injury were treated with a strategy that only included usual supportive measures and high-dose leucovorin. No deaths were directly attributed to complications related to HDMTX. Glucarpidase, an expensive drug, may not be necessary for a significant number of patients.
高剂量甲氨蝶呤(HDMTX)治疗并发的急性肾损伤会增加严重黏膜炎、骨髓抑制和死亡的风险。目前尚不清楚在不使用羧肽酶的情况下,高剂量亚叶酸钙和支持性治疗能否降低HDMTX的毒性。
回顾了2000年1月至2011年12月期间纪念斯隆凯特琳癌症中心所有在给药后48或72小时甲氨蝶呤(MTX)药物水平达到或超过中毒水平10倍的患者的病历。
共确定了88例接受100个疗程HDMTX治疗的患者(中位年龄51岁,范围9 - 90岁)。血清肌酐较基线水平升高了2倍(中位值,范围1至10倍),但所有患者的肾功能均恢复。给药后24、48和72小时MTX的血清水平分别为69 μmol/L(中位值,范围2.2 - 400)、6.9 μmol/L(1.3 - 64)和2.0 μmol/L(0.05 - 26)。给药后48、72、96和120小时的MTX水平之间存在统计学显著相关性,但24至72小时或后续时间点之间不存在相关性。在大多数情况下,81%的疗程按照机构方案给予了高剂量亚叶酸钙。42%的患者出现骨髓抑制;29%的患者出现III级或更高等级的中性粒细胞减少,25%的患者出现血小板减少。分别有21%、17%和6%的患者发生感染并发症、口腔黏膜炎和腹泻。发生了5例死亡,均未直接归因于MTX给药的并发症。在研究期间,另有7例患者根据主治医生的判断接受了羧肽酶治疗,结果另行报告。
100例HDMTX相关急性肾损伤患者采用了仅包括常规支持措施和高剂量亚叶酸钙的治疗策略。没有死亡直接归因于与HDMTX相关的并发症。羧肽酶这种昂贵的药物,对于大量患者可能并非必要。