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Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil
BACKGROUND: The body composition of patients has been associated with tolerability and effectiveness of anticancer therapy. This study aimed to assess the influence of the skeletal muscle index (SMI) on the pharmacokinetics and toxicity of fluorouracil. METHODS: Patients treated in an oncological pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939223/ https://www.ncbi.nlm.nih.gov/pubmed/35941837 http://dx.doi.org/10.1002/cam4.5118 |
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author | Schmulenson, Eduard Zimmermann, Nigina Müller, Lothar Kapsa, Stefanie Sihinevich, Iryna Jaehde, Ulrich |
author_facet | Schmulenson, Eduard Zimmermann, Nigina Müller, Lothar Kapsa, Stefanie Sihinevich, Iryna Jaehde, Ulrich |
author_sort | Schmulenson, Eduard |
collection | PubMed |
description | BACKGROUND: The body composition of patients has been associated with tolerability and effectiveness of anticancer therapy. This study aimed to assess the influence of the skeletal muscle index (SMI) on the pharmacokinetics and toxicity of fluorouracil. METHODS: Patients treated in an oncological practice with fluorouracil‐based chemotherapy and undergoing therapeutic drug monitoring were retrospectively investigated. Computed tomography images were analyzed to measure abdominal skeletal muscle areas in Hounsfield units for the psoas major muscle, back and total skeletal muscle to determine the SMI. For the latter, an automated segmentation method was used additionally. SMI measures were tested as covariates on fluorouracil clearance in a population pharmacokinetic model. Furthermore, regression analyses were performed to analyze the influence of SMI measures on the probability of clinically relevant adverse events (CTCAE grades ≥ 2). RESULTS: Fluorouracil plasma concentrations of 111 patients were available. Covariate analyses showed significant improvements of the model fit by all SMI measures. However, interindividual variability of fluorouracil clearance was only slightly reduced, whereas the SMI of the back muscle showed the largest reduction (−1.1 percentage points). Lower SMI values of the back muscle increased the probability for polyneuropathy and lower SMI of the psoas increased the probability for fatigue. CONCLUSIONS: Our results suggest that pharmacokinetics and toxicity of fluorouracil may be associated with specific SMI measures which deserve further investigation. |
format | Online Article Text |
id | pubmed-9939223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99392232023-02-20 Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil Schmulenson, Eduard Zimmermann, Nigina Müller, Lothar Kapsa, Stefanie Sihinevich, Iryna Jaehde, Ulrich Cancer Med RESEARCH ARTICLES BACKGROUND: The body composition of patients has been associated with tolerability and effectiveness of anticancer therapy. This study aimed to assess the influence of the skeletal muscle index (SMI) on the pharmacokinetics and toxicity of fluorouracil. METHODS: Patients treated in an oncological practice with fluorouracil‐based chemotherapy and undergoing therapeutic drug monitoring were retrospectively investigated. Computed tomography images were analyzed to measure abdominal skeletal muscle areas in Hounsfield units for the psoas major muscle, back and total skeletal muscle to determine the SMI. For the latter, an automated segmentation method was used additionally. SMI measures were tested as covariates on fluorouracil clearance in a population pharmacokinetic model. Furthermore, regression analyses were performed to analyze the influence of SMI measures on the probability of clinically relevant adverse events (CTCAE grades ≥ 2). RESULTS: Fluorouracil plasma concentrations of 111 patients were available. Covariate analyses showed significant improvements of the model fit by all SMI measures. However, interindividual variability of fluorouracil clearance was only slightly reduced, whereas the SMI of the back muscle showed the largest reduction (−1.1 percentage points). Lower SMI values of the back muscle increased the probability for polyneuropathy and lower SMI of the psoas increased the probability for fatigue. CONCLUSIONS: Our results suggest that pharmacokinetics and toxicity of fluorouracil may be associated with specific SMI measures which deserve further investigation. John Wiley and Sons Inc. 2022-08-08 /pmc/articles/PMC9939223/ /pubmed/35941837 http://dx.doi.org/10.1002/cam4.5118 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Schmulenson, Eduard Zimmermann, Nigina Müller, Lothar Kapsa, Stefanie Sihinevich, Iryna Jaehde, Ulrich Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title | Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title_full | Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title_fullStr | Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title_full_unstemmed | Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title_short | Influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
title_sort | influence of the skeletal muscle index on pharmacokinetics and toxicity of fluorouracil |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939223/ https://www.ncbi.nlm.nih.gov/pubmed/35941837 http://dx.doi.org/10.1002/cam4.5118 |
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