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The impact of primary colorectal cancer treatment on physical symptoms and functioning in the first two years: results from the colorectal well-being (CREW) cohort study

Foster, Claire; Haviland, Joanne; Winter, Jane; Grimmett, Chloe; Chivers Seymour, Kim; Calman, Lynn; Corner, Jessica; Din, Amy; Fenlon, Deborah; May, Christine M.; Smith, Peter W.; Richardson, Alison

Authors

Claire Foster

Joanne Haviland

Jane Winter

Chloe Grimmett

Kim Chivers Seymour

Lynn Calman

Jessica Corner

Amy Din

Deborah Fenlon

Christine M. May

Peter W. Smith

Alison Richardson



Abstract

Background: Cancer and its treatment can have a considerable long‐term impact. Relatively little is known about what this means in relation to health and well‐being, how to prepare patients for what to expect, and to tailor support.
Aims: The aim of this study is to describe the impact of colorectal cancer treatment and patient characteristics including self‐efficacy (confidence to self‐manage illness‐related problems) on symptoms and functioning following curative intent surgery.
Methods: Eight hundred fifty‐seven colorectal cancer patients (Dukes' A–C) recruited 2010–2012 from 29 UK centres. Questionnaires pre‐surgery (baseline), 3, 9, 15 and 24 months included assessments of symptoms, functioning and patient characteristics. Regression analyses assessed change in functioning and symptoms over time and associations with socio‐demographic, clinical, treatment and pre‐surgery psychosocial characteristics.
Results: Most problematic symptoms over follow‐up: impotence (45% moderate/severe problems at 24 months), urinary frequency (34%), fatigue (24%), stool frequency (22%), insomnia (20%), flatulence (20%) and pain (16%). Symptoms worsened immediately following surgery and then most improved significantly, generally from 15 months, although some remained as prevalent (impotence and flatulence). Urinary incontinence significantly worsened (mostly changes from none to mild symptoms). From multiple regressions, risk factors consistently statistically significantly associated with worse symptoms and poorer functioning were, worse depression and lower self‐efficacy at baseline, more comorbidities and having a stoma. Tumour site, neo‐adjuvant and adjuvant treatment had little effect.
Conclusions: Most symptoms improve by 15 months following colorectal cancer treatment although some persist. Pre‐surgery self‐efficacy and depression are important predictors of symptoms and functioning, independent of clinical and treatment factors, and amenable to interventions to improve recovery.

Citation

Foster, C., Haviland, J., Winter, J., Grimmett, C., Chivers Seymour, K., Calman, L., …Richardson, A. (2016). The impact of primary colorectal cancer treatment on physical symptoms and functioning in the first two years: results from the colorectal well-being (CREW) cohort study. Psycho-Oncology, 25(S1), 1-22. https://doi.org/10.1002/pon.4077

Journal Article Type Article
Acceptance Date Jan 4, 2016
Online Publication Date Feb 29, 2016
Publication Date Mar 30, 2016
Deposit Date Mar 14, 2016
Journal Psycho-Oncology
Print ISSN 1057-9249
Electronic ISSN 1099-1611
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 25
Issue S1
Pages 1-22
DOI https://doi.org/10.1002/pon.4077
Public URL https://nottingham-repository.worktribe.com/output/977721
Publisher URL http://onlinelibrary.wiley.com/doi/10.1002/pon.4077/full
Additional Information Abstract of the presentation at the British Psychosocial Oncology Society 2016 Annual Conference, 3–4 March 2016, Cambridge, UK.

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