Health-related quality of life among women with breast cancer – a population-based study

Authors

  • Marie Høyer Regional Oncologic Centre, Uppsala University Hospital, Uppsala, Sweden; Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden
  • Birgitta Johansson Department of Oncology, Uppsala University Hospital, Uppsala, Sweden
  • Karin Nordin Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden; Department of Public Health and Primary Health Care, University of Bergen, Bergen, Norway
  • Leif Bergkvist Department of Surgery and Center for Clinical Research, Uppsala University, Central Hospital, Västerås, Sweden
  • Johan Ahlgren Department of Oncology, Gävle Hospital, Gävle, Sweden; Centre of Clinical Research, Uppsala University and County of Gävleborg, Gävle, Sweden
  • Annika Lidin-Lindqvist Regional Oncologic Centre, Uppsala University Hospital, Uppsala, Sweden
  • Mats Lambe Regional Oncologic Centre, Uppsala University Hospital, Uppsala, Sweden; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden
  • Claudia Lampic Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Stockholm, Sweden

DOI:

https://doi.org/10.3109/0284186X.2011.577446

Abstract

Background. High incidence rates of breast cancer emphasize the importance of increased knowledge about the health-related quality of life (HRQoL) in this patient group. The aim of the present study was to describe and compare HRQoL among breast cancer patients shortly after diagnosis with normative data from the general population, and to investigate how clinical, demographic, and socio-economic factors and social support are associated with HRQoL. Material and methods. Participants were identified in a population-based Breast Cancer Quality Register in central Sweden. Of 1573 women newly diagnosed with breast cancer during a one-year period (2007–2008), 69% (n = 1086) completed a questionnaire including the EORTC QLQ-C30, BR23 and the HADS. Results. Compared to age-adjusted normative data, breast cancer patients (mean age 62 years, range 25–94), especially younger women (<50 years), experienced clinically meaningful poorer HRQoL. Clinically significant levels of anxiety and depressive symptoms were found among 14% and 6% of the patients, respectively. Factors associated with more problems/symptoms among study participants included chemotherapy, lack of social support, sick leave and a poor financial situation. Adding socio-economic factors diminished the association between age and HRQoL (p > 0.05). Conclusion. Recently diagnosed breast cancer patients reported poorer HRQoL in several dimensions compared to normative data. In addition to clinical and demographic factors, an unfavorable socio-economic standing was associated with more problems/symptoms. The present findings emphasize the importance of taking a variety of factors into account when assessing HRQoL in the clinical setting.

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Published

2011-10-01

How to Cite

Høyer, M., Johansson, B., Nordin, K., Bergkvist, L., Ahlgren, J., Lidin-Lindqvist, A., … Lampic, C. (2011). Health-related quality of life among women with breast cancer – a population-based study. Acta Oncologica, 50(7), 1015–1026. https://doi.org/10.3109/0284186X.2011.577446