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dc.contributor.authorPoort, H
dc.contributor.authorvan der Graaf, WTA
dc.contributor.authorTielen, R
dc.contributor.authorVlenterie, M
dc.contributor.authorCusters, JAE
dc.contributor.authorPrins, JB
dc.contributor.authorVerhagen, CAHHVM
dc.contributor.authorGielissen, MFM
dc.contributor.authorKnoop, H
dc.date.accessioned2016-12-19T15:09:02Z
dc.date.issued2016-08
dc.identifier.citationJournal of pain and symptom management, 2016, 52 (2), pp. 265 - 271
dc.identifier.issn0885-3924
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/343
dc.identifier.eissn1873-6513
dc.identifier.doi10.1016/j.jpainsymman.2016.02.019
dc.description.abstractContext The introduction of the tyrosine kinase inhibitor (TKI) imatinib in the treatment of gastrointestinal stromal tumor (GIST) in 2000 was the start of a new era of targeted treatment. Since then, the median survival of patients with GIST has substantially increased. Prolonged survival and chronic TKI use are associated with treatment-induced symptoms, such as fatigue, which can compromise quality of life (QoL).Objectives This study determined the prevalence of severe fatigue in GIST patients compared to matched healthy controls, the impact of fatigue on daily life, and associations between fatigue and current TKI use.Methods One hundred nineteen patients treated with surgery and/or a TKI for GIST were asked to participate. Participants completed questionnaires including the Checklist Individual Strength-Fatigue Severity scale (CIS-fatigue), Short-Form 36-Item Health Survey, European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30, Fatigue Catastrophizing Scale, Self-Efficacy Scale, and the Hospital Anxiety and Depression Scale.Results Eighty-nine GIST patients (75%) completed questionnaires, 61 patients (69%) were on a TKI. Prevalence of severe fatigue measured with CIS-fatigue was significantly higher in GIST patients (30%) than in 234 matched healthy controls (15%). The prevalence of severe fatigue did not differ significantly between patients receiving treatment with curative (29%) or palliative intent (36%). Severely fatigued patients reported lower QoL and more impairment on all functional domains. TKI use, more psychological distress, and lower physical functioning were associated with fatigue.Conclusion Severe fatigue occurs in 30% of GIST patients and in 33% of GIST patients on a TKI. The fatigue is disabling and is not only associated with current TKI use but also with psychological distress and physical functioning. GIST patients should be informed about these associated factors of fatigue that deserve appropriate management.
dc.formatPrint-Electronic
dc.format.extent265 - 271
dc.languageeng
dc.language.isoeng
dc.subjectHumans
dc.subjectGastrointestinal Neoplasms
dc.subjectGastrointestinal Stromal Tumors
dc.subjectFatigue
dc.subjectProtein Kinase Inhibitors
dc.subjectSeverity of Illness Index
dc.subjectPrevalence
dc.subjectCross-Sectional Studies
dc.subjectQuality of Life
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.titlePrevalence, Impact, and Correlates of Severe Fatigue in Patients With Gastrointestinal Stromal Tumors.
dc.typeJournal Article
dcterms.dateAccepted2016-02-19
rioxxterms.versionofrecord10.1016/j.jpainsymman.2016.02.019
rioxxterms.licenseref.startdate2016-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfJournal of pain and symptom management
pubs.issue2
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical and Translational Sarcoma
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical and Translational Sarcoma
pubs.publication-statusPublished
pubs.volume52
pubs.embargo.termsNot known
icr.researchteamClinical and Translational Sarcoma
dc.contributor.icrauthorvan der Graaf, Wilhelmina


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