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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Main Authors: 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
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-09-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fphar.2016.00310/full
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spelling 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
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