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Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions

BACKGROUND: Etoposide is a chemotherapeutic agent, widely used for the treatment of various malignancies, including small cell lung cancer (SCLC), an aggressive disease with poor prognosis. Oral etoposide administration exhibits advantages for the quality of life of the patient as well as economic b...

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Autores principales: Rezonja, Renata, Knez, Lea, Cufer, Tanja, Mrhar, Ales
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita, Warsaw 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573828/
https://www.ncbi.nlm.nih.gov/pubmed/23450046
http://dx.doi.org/10.2478/raon-2013-0008
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author Rezonja, Renata
Knez, Lea
Cufer, Tanja
Mrhar, Ales
author_facet Rezonja, Renata
Knez, Lea
Cufer, Tanja
Mrhar, Ales
author_sort Rezonja, Renata
collection PubMed
description BACKGROUND: Etoposide is a chemotherapeutic agent, widely used for the treatment of various malignancies, including small cell lung cancer (SCLC), an aggressive disease with poor prognosis. Oral etoposide administration exhibits advantages for the quality of life of the patient as well as economic benefits. However, widespread use of oral etoposide is limited by incomplete and variable bioavailability. Variability in bioavailability was observed both within and between patients. This suggests that some patients may experience suboptimal tumor cytotoxicity, whereas other patients may be at risk for excess toxicity. CONCLUSIONS: The article highlights dilemmas as well as solutions regarding oral treatment with etoposide by presenting and analyzing relevant literature data. Numerous studies have shown that bioavailability of etoposide is influenced by genetic, physiological and environmental factors. Several strategies were explored to improve bioavailability and to reduce pharmacokinetic variability of oral etoposide, including desired and undesired drug interactions (e.g. with ketoconazole), development of suitable drug delivery systems, use of more water-soluble prodrug of etoposide, and influence on gastric emptying. In addition to genotype-based dose administration, etoposide is suitable for pharmacokinetically guided dosing, which enables dose adjustments in individual patient. Further, it is established that oral and intravenous schedules of etoposide in SCLC patients do not result in significant differences in treatment outcome, while results of toxicity are inconclusive. To conclude, the main message of the article is that better prediction of the pharmacokinetics of oral etoposide may encourage its wider use in routine clinical practice.
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spelling pubmed-35738282013-03-01 Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions Rezonja, Renata Knez, Lea Cufer, Tanja Mrhar, Ales Radiol Oncol Review BACKGROUND: Etoposide is a chemotherapeutic agent, widely used for the treatment of various malignancies, including small cell lung cancer (SCLC), an aggressive disease with poor prognosis. Oral etoposide administration exhibits advantages for the quality of life of the patient as well as economic benefits. However, widespread use of oral etoposide is limited by incomplete and variable bioavailability. Variability in bioavailability was observed both within and between patients. This suggests that some patients may experience suboptimal tumor cytotoxicity, whereas other patients may be at risk for excess toxicity. CONCLUSIONS: The article highlights dilemmas as well as solutions regarding oral treatment with etoposide by presenting and analyzing relevant literature data. Numerous studies have shown that bioavailability of etoposide is influenced by genetic, physiological and environmental factors. Several strategies were explored to improve bioavailability and to reduce pharmacokinetic variability of oral etoposide, including desired and undesired drug interactions (e.g. with ketoconazole), development of suitable drug delivery systems, use of more water-soluble prodrug of etoposide, and influence on gastric emptying. In addition to genotype-based dose administration, etoposide is suitable for pharmacokinetically guided dosing, which enables dose adjustments in individual patient. Further, it is established that oral and intravenous schedules of etoposide in SCLC patients do not result in significant differences in treatment outcome, while results of toxicity are inconclusive. To conclude, the main message of the article is that better prediction of the pharmacokinetics of oral etoposide may encourage its wider use in routine clinical practice. Versita, Warsaw 2013-02-01 /pmc/articles/PMC3573828/ /pubmed/23450046 http://dx.doi.org/10.2478/raon-2013-0008 Text en Copyright © by Association of Radiology & Oncology http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Rezonja, Renata
Knez, Lea
Cufer, Tanja
Mrhar, Ales
Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title_full Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title_fullStr Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title_full_unstemmed Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title_short Oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
title_sort oral treatment with etoposide in small cell lung cancer – dilemmas and solutions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573828/
https://www.ncbi.nlm.nih.gov/pubmed/23450046
http://dx.doi.org/10.2478/raon-2013-0008
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