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Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate
BACKGROUND: High-dose methotrexate (HDMTX) is used in the treatment of certain malignancies, including leptomeningeal metastases, systemic non-Hodgkin lymphoma, acute lymphoblastic leukemia, and osteosarcoma. High circulating levels of methotrexate can cause severe myelosuppression. The present stud...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782285/ https://www.ncbi.nlm.nih.gov/pubmed/26958349 http://dx.doi.org/10.1186/s40780-016-0042-y |
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author | Kaneko, Tetsuya Fujioka, Takashi Suzuki, Yosuke Sato, Yuhki Itoh, Hiroki |
author_facet | Kaneko, Tetsuya Fujioka, Takashi Suzuki, Yosuke Sato, Yuhki Itoh, Hiroki |
author_sort | Kaneko, Tetsuya |
collection | PubMed |
description | BACKGROUND: High-dose methotrexate (HDMTX) is used in the treatment of certain malignancies, including leptomeningeal metastases, systemic non-Hodgkin lymphoma, acute lymphoblastic leukemia, and osteosarcoma. High circulating levels of methotrexate can cause severe myelosuppression. The present study aimed to examine the differences in plasma MTX concentrations measured by two immunoassay systems currently available in the Japanese market, a TD(X)/FL(X) analyzer and a TBA-25FR analyzer. METHODS: A total of 69 plasma samples from 16 patients were assayed by a fluorescence polarization immunoassay technique using a TDx/FLx analyzer (Abbott Diagnostics, Chicago, Illinois, U.S.A.) and a homogeneous enzyme immunoassay technique using a TBA-25FR analyzer (Toshiba Medical Systems, Tokyo, Japan). RESULTS: Assay results were very consistent between the two systems, with good correlation 24 h after the start of treatment (TBA-25FR = 1.06・TD(X)/FL(X), −1.31, r = 0.99), 48 h after the start of treatment (TBA-25FR = 1.00・TD(X)/FL(X), +0.027, r > 0.99), and 72 h after the start of treatment (TBA-25FR = 1.09・TD(X)/FL(X), +0.011, r > 0.99). CONCLUSIONS: The calibration curve spanned one order of magnitude with a linear working range from the lowest to the highest standard. The standard deviations show the excellent reproducibility of repeated measurements at each standard level for both immunoassay systems. However, when using the TBA-25FR, it is necessary to perform measurements in the low-concentration range with care. |
format | Online Article Text |
id | pubmed-4782285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47822852016-03-09 Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate Kaneko, Tetsuya Fujioka, Takashi Suzuki, Yosuke Sato, Yuhki Itoh, Hiroki J Pharm Health Care Sci Short Report BACKGROUND: High-dose methotrexate (HDMTX) is used in the treatment of certain malignancies, including leptomeningeal metastases, systemic non-Hodgkin lymphoma, acute lymphoblastic leukemia, and osteosarcoma. High circulating levels of methotrexate can cause severe myelosuppression. The present study aimed to examine the differences in plasma MTX concentrations measured by two immunoassay systems currently available in the Japanese market, a TD(X)/FL(X) analyzer and a TBA-25FR analyzer. METHODS: A total of 69 plasma samples from 16 patients were assayed by a fluorescence polarization immunoassay technique using a TDx/FLx analyzer (Abbott Diagnostics, Chicago, Illinois, U.S.A.) and a homogeneous enzyme immunoassay technique using a TBA-25FR analyzer (Toshiba Medical Systems, Tokyo, Japan). RESULTS: Assay results were very consistent between the two systems, with good correlation 24 h after the start of treatment (TBA-25FR = 1.06・TD(X)/FL(X), −1.31, r = 0.99), 48 h after the start of treatment (TBA-25FR = 1.00・TD(X)/FL(X), +0.027, r > 0.99), and 72 h after the start of treatment (TBA-25FR = 1.09・TD(X)/FL(X), +0.011, r > 0.99). CONCLUSIONS: The calibration curve spanned one order of magnitude with a linear working range from the lowest to the highest standard. The standard deviations show the excellent reproducibility of repeated measurements at each standard level for both immunoassay systems. However, when using the TBA-25FR, it is necessary to perform measurements in the low-concentration range with care. BioMed Central 2016-03-08 /pmc/articles/PMC4782285/ /pubmed/26958349 http://dx.doi.org/10.1186/s40780-016-0042-y Text en © Kaneko et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Kaneko, Tetsuya Fujioka, Takashi Suzuki, Yosuke Sato, Yuhki Itoh, Hiroki Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title | Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title_full | Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title_fullStr | Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title_full_unstemmed | Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title_short | Performance characteristics between TDx®FLx and TBA™-25FR for the therapeutic drug monitoring of methotrexate |
title_sort | performance characteristics between tdx®flx and tba™-25fr for the therapeutic drug monitoring of methotrexate |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782285/ https://www.ncbi.nlm.nih.gov/pubmed/26958349 http://dx.doi.org/10.1186/s40780-016-0042-y |
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