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Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia
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 previo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615715/ https://www.ncbi.nlm.nih.gov/pubmed/31308758 http://dx.doi.org/10.2147/CMAR.S207959 |
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author | Li, Xiao Sui, Zhongguo Jing, Fanbo Xu, Wen Li, Xiangpeng Guo, Qie Sun, Shuhong Bi, Xiaolin |
author_facet | Li, Xiao Sui, Zhongguo Jing, Fanbo Xu, Wen Li, Xiangpeng Guo, Qie Sun, Shuhong Bi, Xiaolin |
author_sort | Li, Xiao |
collection | PubMed |
description | 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 μmol/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. |
format | Online Article Text |
id | pubmed-6615715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66157152019-07-15 Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia Li, Xiao Sui, Zhongguo Jing, Fanbo Xu, Wen Li, Xiangpeng Guo, Qie Sun, Shuhong Bi, Xiaolin Cancer Manag Res Original Research 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 μmol/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. Dove 2019-07-05 /pmc/articles/PMC6615715/ /pubmed/31308758 http://dx.doi.org/10.2147/CMAR.S207959 Text en © 2019 Li et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Li, Xiao Sui, Zhongguo Jing, Fanbo Xu, Wen Li, Xiangpeng Guo, Qie Sun, Shuhong Bi, Xiaolin Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title | Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title_full | Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title_fullStr | Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title_full_unstemmed | Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title_short | Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
title_sort | identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615715/ https://www.ncbi.nlm.nih.gov/pubmed/31308758 http://dx.doi.org/10.2147/CMAR.S207959 |
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