Article Text
Abstract
Background We assessed the prevalence of self-reported perceived discrimination in the workplace after the end of treatment among breast cancer (BC) survivors and studied its association with social, health-related and work-related factors.
Methods We used data from a French prospective cohort (CANcer TOxicities) including women diagnosed with stage I–III BC. Our analysis included 2130 women who were employed, <57 years old at BC diagnosis and were working 2 years afterwards. We assessed the association between social, health-related and work-related factors and perceived discrimination in the workplace using logistic regression models.
Results Overall, 26% of women reported perceived discrimination in the workplace after the end of treatment. Women working for a small company, in the public sector or with better overall health status were less likely to report perceived discrimination. Women who benefited from easing dispositions at their workplace, who did not feel supported by their colleagues and those who returned to work because of fear of job loss were more likely to report perceived discrimination.
Conclusions One in four BC survivors perceives discrimination in the workplace. Health and work-related factors are associated with increased likelihood of reporting perceived discrimination.
Trial registration number NCT01993498.
- EPIDEMIOLOGY
- PUBLIC HEALTH
- LONGITUDINAL STUDIES
- QUALITY OF LIFE
Data availability statement
Data may be obtained from a third party and are not publicly available. CANTO data are not publicly available and can be obtained from UNICANCER. La Vie Deux Ans Après Un Diagnostic de Cancer - 2012, INSERM, INCa (Producteurs), ADISP (Diffuseur) data are not publicly available and can be obtained from Quetelet PROGEDO.
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Data availability statement
Data may be obtained from a third party and are not publicly available. CANTO data are not publicly available and can be obtained from UNICANCER. La Vie Deux Ans Après Un Diagnostic de Cancer - 2012, INSERM, INCa (Producteurs), ADISP (Diffuseur) data are not publicly available and can be obtained from Quetelet PROGEDO.
Footnotes
Contributors Conception and design: GRDA and GM. Administrative support: SE and A-LM. Provision of study material or patients: BP, CC, PC, PR, AA, OA, MI, JW and RR. Collection and assembly of data: IV-L, TB, ADM, JH, AD and GM. Data analysis and interpretation: GRDA, GM, IV-L, ADM, EC and AD. Manuscript writing: all authors. Final approval of manuscript: all authors. Accountable for all aspects of the work: all authors. Guarantor: GM
Funding The authors of this paper thank Quetelet PROGEDO for sharing their data. This research was supported by the French Government under the 'Investment for the Future' programme managed by the National Research Agency (ANR), grant n° ANR-10-COHO-0004 and ARC (number PGA1 RF20170205420).
Competing interests BP: consulting/advisor: Puma Biotechnology, Novartis, Myriad Genetics and Pierre Fabre; personal fees: Novartis, AstraZeneca, MSD Oncology and Pfizer; research funding: Daiichi, Puma Biotechnology, Novartis, Merus, Pfizer and AstraZeneca.
Provenance and peer review Not commissioned; externally peer reviewed.
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