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

被引:193
|
作者
van Leeuwen, R. W. F. [1 ,2 ]
Brundel, D. H. S. [2 ]
Neef, C. [2 ]
van Gelder, T. [1 ,3 ,4 ]
Mathijssen, R. H. J. [5 ]
Burger, D. M. [6 ]
Jansman, F. G. A. [7 ,8 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Pharm, NL-3015 CE Rotterdam, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Clin Pharm & Toxicol, NL-6229 HX Maastricht, Netherlands
[3] Erasmus Univ, Med Ctr, Dept Internal Med, NL-3015 CE Rotterdam, Netherlands
[4] Erasmus Univ, Med Ctr, Dept Hosp Pharm, NL-3015 CE Rotterdam, Netherlands
[5] Erasmus Univ, Med Ctr, Daniel den Hoed Canc Ctr, Dept Med Oncol, NL-3015 CE Rotterdam, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Radboud Univ Ctr Oncol RUCO, Dept Pharm, NL-6526 GA Nijmegen, Netherlands
[7] Deventer Hosp, Dept Clin Pharm, NL-7416 SE Deventer, Netherlands
[8] Univ Groningen, Dept Pharmacotherapy & Pharmaceut Care, NL-9713 AV Groningen, Netherlands
关键词
chemotherapy; potential drug-drug interactions; oncology; pharmacology; risk factors; LOW-DOSE METHOTREXATE; IRINOTECAN METABOLISM; RHEUMATOID-ARTHRITIS; MEDICAL PATIENTS; ELDERLY PERSONS; OLDER-PEOPLE; FALLS; PHARMACOKINETICS; METAANALYSIS; FLUCONAZOLE;
D O I
10.1038/bjc.2013.48
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1071 / 1078
页数:8
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