Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia

被引:14
|
作者
Li, Xiao [1 ]
Sui, Zhongguo [1 ]
Jing, Fanbo [1 ]
Xu, Wen [1 ]
Li, Xiangpeng [1 ]
Guo, Qie [1 ]
Sun, Shuhong [1 ]
Bi, Xiaolin [2 ]
机构
[1] Qingdao Univ, Dept Clin Pharm, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Shandong, Peoples R China
[2] Qingdao Univ, Dept Nutr, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Shandong, Peoples R China
来源
关键词
high-dose methotrexate; methotrexate concentration; toxicities; patient characteristics; risk predictors; acute lymphoblastic leukemia; PLASMA METHOTREXATE; ORAL MUCOSITIS; THERAPY; ASSOCIATION; DYSFUNCTION; CREATININE; PREDICT;
D O I
10.2147/CMAR.S207959
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Whether monitoring of the methotrexate (MTX) concentrations after high-dose MTX (HD-MTX) infusion can predict toxicities is still controversial, especially when HD-MTX therapy is used in the treatment of children with acute lymphoblastic leukemia (ALL), which is different than the previous schedules. The relationship between patient characteristics and severe adverse events (AEs) has yet to be determined. Objective: To analyze the relationship between the MTX concentration and toxicities and to identify the risk predictors from patient characteristics for severe AEs during HD-MTX therapy in children with ALL. Methods: We conducted a retrospective study on children with ALL who were treated with 388 HD-MTX infusions. The chi-square test and univariate and logistic regression analyses were used to analyze the relationship between the MTX concentrations and toxicities and to identify predictors for severe AEs. Results: Febrile neutropenia (P=0.000) and vomiting (P=0.034) were more likely to occur if the infusion had an MTX level >= 1 mu mol/L at 44 h, but other toxicities had no correlations with MTX concentration. Predictive factors for toxicities were as follows: higher risk stratification and higher values of albumin (ALB) for leucopenia, higher values of white blood cell count (WBC) for anemia, higher values of ALB and creatinine (Cr) for neutropenia, higher risk stratification and higher 44-h MTX concentration for febrile neutropenia, higher values of alanine transferase (ALT) for elevated ALT, higher values of ALT for elevated aspartate transferase (AST), and higher values of total bilirubin (TBil) for vomiting. Conclusion: Routine monitoring of 44-h MTX concentrations is essential to identify patients at high risk of developing febrile neutropenia and vomiting. This study may provide a reference for clinicians to distinguish patients with a relatively high risk of severe AEs based on certain characteristics before HD-MTX infusion.
引用
收藏
页码:6265 / 6274
页数:10
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