Villegas Rubio Jose A, Cacciavillano Walter, Rose Adriana, Zubizarreta Pedro, Scopinaro Marcelo
Hematology/Oncology Department, Professor Doctor Juan P. Garrahan Children Hospital, Buenos Aires, Argentina.
J Pediatr Hematol Oncol. 2017 Oct;39(7):e349-e352. doi: 10.1097/MPH.0000000000000922.
The purpose of this study was to evaluate the feasibility and safety of ambulatory high-dose methotrexate (HDMTX) administration with oral hydration, alkalinization, and leucovorin rescue. HDMTX (12 g/m) was given intravenously over 4 hours after urine alkalinization. Families and patients were instructed to continue ambulatory oral hydration and alkalinization to monitor urine pH and to adjust bicarbonate according to our institution's treatment algorithm. Clinical status and MTX levels were controlled every 24 hours, and oral leucovorin dose was adjusted accordingly.
From April 2007 to December 2010, 150 of 447 courses of HDMTX (31.4%) were given on an outpatient basis, and 91.2% were successfully completed. The main causes of failure were poor oral tolerance (n=6) and fever (n=4). Most patients (81%) had MTX levels of <10 μmol/L 24 hours post-HDMTX; only in 1 course the levels were >50 μmol/L (50.96 μmol/L). Neutropenia grade III/IV was observed in 18.3% of the courses, grade III/IV leukopenia in 2.7%, and grade III/IV thrombocytopenia and anemia in 4.7%. Around 39% were associated with grade III/IV hepatic toxicity (asymptomatic hypertransaminasemia), grade III-IV gastrointestinal toxicity (vomiting and diarrhea) (5%), grade III-IV mucositis (4%), and none of the patients developed renal toxicity.
Ambulatory HDMTX administration is feasible and safe in a population with poor resources in a developing country.
本研究的目的是评估门诊大剂量甲氨蝶呤(HDMTX)给药联合口服补液、碱化尿液及亚叶酸钙解救的可行性和安全性。在尿液碱化后,HDMTX(12 g/m²)于4小时内静脉输注。指导家属和患者持续进行门诊口服补液和尿液碱化,以监测尿液pH值,并根据本机构的治疗方案调整碳酸氢盐用量。每24小时监测临床状态和甲氨蝶呤水平,并据此调整口服亚叶酸钙剂量。
2007年4月至2010年12月,447个HDMTX疗程中有150个(31.4%)在门诊给药,91.2%成功完成。失败的主要原因是口服耐受性差(n = 6)和发热(n = 4)。大多数患者(81%)在HDMTX给药后24小时甲氨蝶呤水平<10 μmol/L;仅1个疗程水平>50 μmol/L(50.96 μmol/L)。18.3%的疗程观察到III/IV级中性粒细胞减少,2.7%为III/IV级白细胞减少,4.7%为III/IV级血小板减少和贫血。约39%与III/IV级肝毒性(无症状性转氨酶升高)、III-IV级胃肠道毒性(呕吐和腹泻)(5%)、III-IV级粘膜炎(4%)相关,且无患者发生肾毒性。
在发展中国家资源匮乏的人群中,门诊HDMTX给药是可行且安全的。