Cargando…

Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs

BACKGROUND: Potential drug–drug interactions (PDDIs) in patients with cancer are common, but have not previously been quantified for oral anticancer treatment. We assessed the prevalence and seriousness of potential PDDIs among ambulatory cancer patients on oral anticancer treatment. METHODS: A sear...

Descripción completa

Detalles Bibliográficos
Autores principales: van Leeuwen, R W F, Brundel, D H S, Neef, C, van Gelder, T, Mathijssen, R H J, Burger, D M, Jansman, F G A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619066/
https://www.ncbi.nlm.nih.gov/pubmed/23412102
http://dx.doi.org/10.1038/bjc.2013.48
_version_ 1782265458460721152
author van Leeuwen, R W F
Brundel, D H S
Neef, C
van Gelder, T
Mathijssen, R H J
Burger, D M
Jansman, F G A
author_facet van Leeuwen, R W F
Brundel, D H S
Neef, C
van Gelder, T
Mathijssen, R H J
Burger, D M
Jansman, F G A
author_sort van Leeuwen, R W F
collection PubMed
description BACKGROUND: Potential drug–drug interactions (PDDIs) in patients with cancer are common, but have not previously been quantified for oral anticancer treatment. We assessed the prevalence and seriousness of potential PDDIs among ambulatory cancer patients on oral anticancer treatment. METHODS: A search was conducted in a computer-based medication prescription system for dispensing oral anticancer drugs to outpatients in three Dutch centres. Potential drug–drug interactions were identified using electronic (Drug Interaction Fact software) and manual screening methods (peer-reviewed reports). RESULTS: In the 898 patients included in the study, 1359 PDDIs were identified in 426 patients (46%, 95% confidence interval (CI)=42–50%). In 143 patients (16%), a major PDDI was identified. The drug classes most frequently involved in a major PDDI were coumarins and opioids. The majority of cases concerned central nervous system interactions, PDDIs that can cause gastrointestinal toxicity and prolongation of QT intervals. In multivariate analysis, concomitant use of more drugs (odds ratio (OR)=1.66, 95% CI=1.54–1.78, P<0001) and genito-urinary cancer (OR=0.25, 95% CI=0.12–0.52, P<0001) were risk factors. CONCLUSION: Potential drug–drug interactions are very common among cancer patients on oral cancer therapy. Physicians and pharmacists should be more aware of these potential interactions.
format Online
Article
Text
id pubmed-3619066
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-36190662014-03-19 Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs van Leeuwen, R W F Brundel, D H S Neef, C van Gelder, T Mathijssen, R H J Burger, D M Jansman, F G A Br J Cancer Translational Therapeutics BACKGROUND: Potential drug–drug interactions (PDDIs) in patients with cancer are common, but have not previously been quantified for oral anticancer treatment. We assessed the prevalence and seriousness of potential PDDIs among ambulatory cancer patients on oral anticancer treatment. METHODS: A search was conducted in a computer-based medication prescription system for dispensing oral anticancer drugs to outpatients in three Dutch centres. Potential drug–drug interactions were identified using electronic (Drug Interaction Fact software) and manual screening methods (peer-reviewed reports). RESULTS: In the 898 patients included in the study, 1359 PDDIs were identified in 426 patients (46%, 95% confidence interval (CI)=42–50%). In 143 patients (16%), a major PDDI was identified. The drug classes most frequently involved in a major PDDI were coumarins and opioids. The majority of cases concerned central nervous system interactions, PDDIs that can cause gastrointestinal toxicity and prolongation of QT intervals. In multivariate analysis, concomitant use of more drugs (odds ratio (OR)=1.66, 95% CI=1.54–1.78, P<0001) and genito-urinary cancer (OR=0.25, 95% CI=0.12–0.52, P<0001) were risk factors. CONCLUSION: Potential drug–drug interactions are very common among cancer patients on oral cancer therapy. Physicians and pharmacists should be more aware of these potential interactions. Nature Publishing Group 2013-03-19 2013-02-14 /pmc/articles/PMC3619066/ /pubmed/23412102 http://dx.doi.org/10.1038/bjc.2013.48 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Translational Therapeutics
van Leeuwen, R W F
Brundel, D H S
Neef, C
van Gelder, T
Mathijssen, R H J
Burger, D M
Jansman, F G A
Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title_full Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title_fullStr Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title_full_unstemmed Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title_short Prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
title_sort prevalence of potential drug–drug interactions in cancer patients treated with oral anticancer drugs
topic Translational Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619066/
https://www.ncbi.nlm.nih.gov/pubmed/23412102
http://dx.doi.org/10.1038/bjc.2013.48
work_keys_str_mv AT vanleeuwenrwf prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT brundeldhs prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT neefc prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT vangeldert prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT mathijssenrhj prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT burgerdm prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs
AT jansmanfga prevalenceofpotentialdrugdruginteractionsincancerpatientstreatedwithoralanticancerdrugs