Adherence and patients’ experiences with the use of capecitabine in daily practice
Background: Capecitabine is a widely prescribed oral anticancer agent. We studied medication adherence and explored its use in daily practice from a patients’ perspective. Methods: Patients (n=92) starting capecitabine were followed up to five 3-week cycles. Adherence was assessed using a pill coun...
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doaj-f99a94804ce34d75914a0025ea090f602020-11-25T00:51:45ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122016-09-01710.3389/fphar.2016.00310198962Adherence and patients’ experiences with the use of capecitabine in daily practiceLonneke Timmers0Christel Boons1Dirk Mangnus2Peter van de Ven3Pieter van den Berg4Aart Beeker5Eleonora Swart6Richard Honeywell7Godefridus Peters8Epie Boven9Jacqueline Hugtenburg10Jacqueline Hugtenburg11VU University Medical CenterVU University Medical CenterSlingeland ZiekenhuisVU University Medical CenterTergooi HospitalSpaarne HospitalVU University Medical CenterVU University Medical CenterVU University Medical CenterVU University Medical CenterVU University Medical CenterVU University Medical CenterBackground: Capecitabine is a widely prescribed oral anticancer agent. We studied medication adherence and explored its use in daily practice from a patients’ perspective. Methods: Patients (n=92) starting capecitabine were followed up to five 3-week cycles. Adherence was assessed using a pill count, pharmacy data and dosing information from the patients’ medical file. Self-reported adherence was measured using the Medication Adherence Report Scale (MARS). At baseline and during week 2 of cycles 1, 3 and 5, patients filled out questionnaires about quality of life, symptoms, attitude towards medicines and disease and use in daily practice. Simultaneously, blood samples were taken to determine the area under the curve (AUC) of 5’-deoxy-5-fluorouridine (5’-DFUR), 5-fluorouracil (5-FU) and α-fluoro-β-alanine (FBAL) by a population pharmacokinetic model. Associations between AUCs and patient-reported symptoms were tested for cycles 3 and 5.Results: Most patients (84/92; 91%) had an adherence rate of ≥95% and ≤105%. The percentage of patients reporting any non-adherence behaviour measured with MARS increased from 16% at cycle 1 to 29% at cycle 5. Symptoms were reported frequently and the dosing regimen was adjusted by the physician at least once in 62% of patients. In multivariate analysis the probability of an adjustment increased with the number of co-medication (OR 1.19, 95%CI:1.03-1.39) and a stronger emotional response to the disease (OR 1.32, 95%CI:1.10-1.59)..The AUC of 5’-DFUR was associated with weight loss (OR 1.10, 95%CI:1.01-1.19), AUC of FBAL with hand-foot syndrome (OR 0.90, 95%CI:0.83-0.99), rhinorrhea (OR 1.21, 95%CI:1.03-1.42 weight loss (OR 1.09, 95%CI:1.00-1.20) and depression (OR 0.90, 95%CI:0.82-0.99). Side effects were reported by one third of patients as the reason to discontinue treatment.Conclusion: Adherence to capecitabine was generally high. Nevertheless, adherence measured with MARS decreased over time Adherence management to support implementation of correct capecitabine use is specifically relevant in longer term treatment. In addition, it appears that adverse event management is important to support persistence. With the extending armamentarium of oral targeted anticancer agents and prolonged treatment duration, we expect the issue of medication adherence of increasing importance in oncology.http://journal.frontiersin.org/Journal/10.3389/fphar.2016.00310/fullMedication AdherencecapecitabinePatient's perspectiveDose adjustmentspatient-reported symptoms |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lonneke Timmers Christel Boons Dirk Mangnus Peter van de Ven Pieter van den Berg Aart Beeker Eleonora Swart Richard Honeywell Godefridus Peters Epie Boven Jacqueline Hugtenburg Jacqueline Hugtenburg |
spellingShingle |
Lonneke Timmers Christel Boons Dirk Mangnus Peter van de Ven Pieter van den Berg Aart Beeker Eleonora Swart Richard Honeywell Godefridus Peters Epie Boven Jacqueline Hugtenburg Jacqueline Hugtenburg Adherence and patients’ experiences with the use of capecitabine in daily practice Frontiers in Pharmacology Medication Adherence capecitabine Patient's perspective Dose adjustments patient-reported symptoms |
author_facet |
Lonneke Timmers Christel Boons Dirk Mangnus Peter van de Ven Pieter van den Berg Aart Beeker Eleonora Swart Richard Honeywell Godefridus Peters Epie Boven Jacqueline Hugtenburg Jacqueline Hugtenburg |
author_sort |
Lonneke Timmers |
title |
Adherence and patients’ experiences with the use of capecitabine in daily practice |
title_short |
Adherence and patients’ experiences with the use of capecitabine in daily practice |
title_full |
Adherence and patients’ experiences with the use of capecitabine in daily practice |
title_fullStr |
Adherence and patients’ experiences with the use of capecitabine in daily practice |
title_full_unstemmed |
Adherence and patients’ experiences with the use of capecitabine in daily practice |
title_sort |
adherence and patients’ experiences with the use of capecitabine in daily practice |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Pharmacology |
issn |
1663-9812 |
publishDate |
2016-09-01 |
description |
Background: Capecitabine is a widely prescribed oral anticancer agent. We studied medication adherence and explored its use in daily practice from a patients’ perspective. Methods: Patients (n=92) starting capecitabine were followed up to five 3-week cycles. Adherence was assessed using a pill count, pharmacy data and dosing information from the patients’ medical file. Self-reported adherence was measured using the Medication Adherence Report Scale (MARS). At baseline and during week 2 of cycles 1, 3 and 5, patients filled out questionnaires about quality of life, symptoms, attitude towards medicines and disease and use in daily practice. Simultaneously, blood samples were taken to determine the area under the curve (AUC) of 5’-deoxy-5-fluorouridine (5’-DFUR), 5-fluorouracil (5-FU) and α-fluoro-β-alanine (FBAL) by a population pharmacokinetic model. Associations between AUCs and patient-reported symptoms were tested for cycles 3 and 5.Results: Most patients (84/92; 91%) had an adherence rate of ≥95% and ≤105%. The percentage of patients reporting any non-adherence behaviour measured with MARS increased from 16% at cycle 1 to 29% at cycle 5. Symptoms were reported frequently and the dosing regimen was adjusted by the physician at least once in 62% of patients. In multivariate analysis the probability of an adjustment increased with the number of co-medication (OR 1.19, 95%CI:1.03-1.39) and a stronger emotional response to the disease (OR 1.32, 95%CI:1.10-1.59)..The AUC of 5’-DFUR was associated with weight loss (OR 1.10, 95%CI:1.01-1.19), AUC of FBAL with hand-foot syndrome (OR 0.90, 95%CI:0.83-0.99), rhinorrhea (OR 1.21, 95%CI:1.03-1.42 weight loss (OR 1.09, 95%CI:1.00-1.20) and depression (OR 0.90, 95%CI:0.82-0.99). Side effects were reported by one third of patients as the reason to discontinue treatment.Conclusion: Adherence to capecitabine was generally high. Nevertheless, adherence measured with MARS decreased over time Adherence management to support implementation of correct capecitabine use is specifically relevant in longer term treatment. In addition, it appears that adverse event management is important to support persistence. With the extending armamentarium of oral targeted anticancer agents and prolonged treatment duration, we expect the issue of medication adherence of increasing importance in oncology. |
topic |
Medication Adherence capecitabine Patient's perspective Dose adjustments patient-reported symptoms |
url |
http://journal.frontiersin.org/Journal/10.3389/fphar.2016.00310/full |
work_keys_str_mv |
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