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An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma

SIMPLE SUMMARY: Oral antitumor therapy has significantly improved clinical outcomes in multiple tumor entities. However, following a standard dosing regime, strong interindividual variability in patients’ plasma concentrations can be observed for many oral antitumor drugs. This results in risks of r...

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Autores principales: Kehl, Niklas, Schlichtig, Katja, Dürr, Pauline, Bellut, Laura, Dörje, Frank, Fietkau, Rainer, Pavel, Marianne, Mackensen, Andreas, Wullich, Bernd, Maas, Renke, Fromm, Martin F., Gessner, Arne, Taudte, R. Verena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699473/
https://www.ncbi.nlm.nih.gov/pubmed/34944950
http://dx.doi.org/10.3390/cancers13246329
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author Kehl, Niklas
Schlichtig, Katja
Dürr, Pauline
Bellut, Laura
Dörje, Frank
Fietkau, Rainer
Pavel, Marianne
Mackensen, Andreas
Wullich, Bernd
Maas, Renke
Fromm, Martin F.
Gessner, Arne
Taudte, R. Verena
author_facet Kehl, Niklas
Schlichtig, Katja
Dürr, Pauline
Bellut, Laura
Dörje, Frank
Fietkau, Rainer
Pavel, Marianne
Mackensen, Andreas
Wullich, Bernd
Maas, Renke
Fromm, Martin F.
Gessner, Arne
Taudte, R. Verena
author_sort Kehl, Niklas
collection PubMed
description SIMPLE SUMMARY: Oral antitumor therapy has significantly improved clinical outcomes in multiple tumor entities. However, following a standard dosing regime, strong interindividual variability in patients’ plasma concentrations can be observed for many oral antitumor drugs. This results in risks of reduced therapeutic effect and increased side effects. Monitoring these variable plasma concentrations is an important tool in evaluating multiple factors influencing drug exposure and, if necessary, adjusting therapeutic doses. Here, we developed a method for the simultaneous measurement of 57 oral antitumor drug plasma concentrations. Detection and quantification were achieved using liquid chromatography coupled to an Orbitrap mass spectrometer, which can be easily expanded to newly approved oral antitumor drugs in the future. Applicability of the method was proven by measuring 71 plasma samples from 39 patients undergoing oral antitumor therapy. In summary, the developed method provides an important tool for exposure measurements of oral antitumor drugs. ABSTRACT: Oral anticancer drugs have led to significant improvements in the treatment of multiple tumor entities. However, in patients undergoing oral antitumor therapy, plasma concentrations are highly variable, resulting in risks of reduced therapeutic effects or an increase in side effects. One important tool to reduce this variability is therapeutic drug monitoring. In this work we describe a method to simultaneously quantify the plasma concentrations of 57 oral antitumor agents. Quantification of these drugs was achieved using liquid chromatography coupled to an Orbitrap mass spectrometer. The method was fully validated according to the FDA guidelines and constitutes a simple and robust way for exposure monitoring of a wide variety of oral anticancer drugs. Applicability to clinical routine was demonstrated by the analysis of 71 plasma samples taken from 39 patients. In summary, this new multi-drug method allows simultaneous quantification of 57 oral antitumor drugs, which can be applied to exposure monitoring in clinical studies, taking into account the broad variety of oral antitumor drugs prescribed in clinical routine.
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spelling pubmed-86994732021-12-24 An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma Kehl, Niklas Schlichtig, Katja Dürr, Pauline Bellut, Laura Dörje, Frank Fietkau, Rainer Pavel, Marianne Mackensen, Andreas Wullich, Bernd Maas, Renke Fromm, Martin F. Gessner, Arne Taudte, R. Verena Cancers (Basel) Article SIMPLE SUMMARY: Oral antitumor therapy has significantly improved clinical outcomes in multiple tumor entities. However, following a standard dosing regime, strong interindividual variability in patients’ plasma concentrations can be observed for many oral antitumor drugs. This results in risks of reduced therapeutic effect and increased side effects. Monitoring these variable plasma concentrations is an important tool in evaluating multiple factors influencing drug exposure and, if necessary, adjusting therapeutic doses. Here, we developed a method for the simultaneous measurement of 57 oral antitumor drug plasma concentrations. Detection and quantification were achieved using liquid chromatography coupled to an Orbitrap mass spectrometer, which can be easily expanded to newly approved oral antitumor drugs in the future. Applicability of the method was proven by measuring 71 plasma samples from 39 patients undergoing oral antitumor therapy. In summary, the developed method provides an important tool for exposure measurements of oral antitumor drugs. ABSTRACT: Oral anticancer drugs have led to significant improvements in the treatment of multiple tumor entities. However, in patients undergoing oral antitumor therapy, plasma concentrations are highly variable, resulting in risks of reduced therapeutic effects or an increase in side effects. One important tool to reduce this variability is therapeutic drug monitoring. In this work we describe a method to simultaneously quantify the plasma concentrations of 57 oral antitumor agents. Quantification of these drugs was achieved using liquid chromatography coupled to an Orbitrap mass spectrometer. The method was fully validated according to the FDA guidelines and constitutes a simple and robust way for exposure monitoring of a wide variety of oral anticancer drugs. Applicability to clinical routine was demonstrated by the analysis of 71 plasma samples taken from 39 patients. In summary, this new multi-drug method allows simultaneous quantification of 57 oral antitumor drugs, which can be applied to exposure monitoring in clinical studies, taking into account the broad variety of oral antitumor drugs prescribed in clinical routine. MDPI 2021-12-16 /pmc/articles/PMC8699473/ /pubmed/34944950 http://dx.doi.org/10.3390/cancers13246329 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kehl, Niklas
Schlichtig, Katja
Dürr, Pauline
Bellut, Laura
Dörje, Frank
Fietkau, Rainer
Pavel, Marianne
Mackensen, Andreas
Wullich, Bernd
Maas, Renke
Fromm, Martin F.
Gessner, Arne
Taudte, R. Verena
An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title_full An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title_fullStr An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title_full_unstemmed An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title_short An Easily Expandable Multi-Drug LC-MS Assay for the Simultaneous Quantification of 57 Oral Antitumor Drugs in Human Plasma
title_sort easily expandable multi-drug lc-ms assay for the simultaneous quantification of 57 oral antitumor drugs in human plasma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699473/
https://www.ncbi.nlm.nih.gov/pubmed/34944950
http://dx.doi.org/10.3390/cancers13246329
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