Abstract
Purpose
Despite limited evidence supporting its effectiveness, most guidelines recommend long-term, routinely scheduled in-person surveillance of patients with early breast cancer (EBC). The COVID-19 pandemic led to increased use of virtual care. This survey evaluated patient perspectives on follow-up care.
Methods
Patients with EBC undergoing surveillance were surveyed about follow-up protocols, perceptions, and interest in clinical trials assessing different follow-up strategies.
Results
Of 402 approached patients 270 completed the survey (response rate 67%). Median age 62.5 years (range 25–86) and median time since breast cancer diagnosis was 3.8 years (range < 1–33 years). Most (n = 148/244, 60%) were followed by more than one provider. Routine follow-ups with breast examination were mostly conducted by medical/radiation oncologists every 6 months (n = 110/236, 46%) or annually (n = 106/236, 44%). Participants felt routine follow-up was useful to monitor for recurrence, manage side effects of cancer treatment and to provide support/reassurance. Most participants felt regular follow-up care would detect recurrent cancer earlier (n = 214/255, 96%) and increase survival (n = 218/249, 88%). The COVID-19 pandemic reduced the number of in-person visits for 54% of patients (n = 63/117). Patients were concerned this reduction of in-person visits would lead to later detection of both local (n = 29/63, 46%) and distant recurrences (n = 25/63, 40%). While many felt their medical and radiation oncologists were the most suited to provide follow-up care, 55% felt comfortable having their primary care provider (PCP) conduct surveillance. When presented with a scenario where follow-up has no effect on earlier detection or survival, 70% of patients still wanted routine in-person follow-up for reassurance (63%) with the goal of earlier recurrence detection (56%).
Conclusions
Despite limited evidence of effectiveness of routine in-person assessment, patients continue to place importance on regularly scheduled in-person follow-up.
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Data Availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on request with approval of the Ontario Cancer Research Ethics Board.
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Acknowledgements
We would like to acknowledge OH-CCO Integrated Cancer Program Funding Agreement as a person-centered funding line item and Jill Taylor and Beth Ciavaglia as our patient representatives.
Funding
This research was supported by the Ottawa Hospital and Cancer Care Ontario’s Integrated Cancer Program initiative which funds patient-centred research as well as the Rethinking Clinical Trials (REaCT) program at the Ottawa Hospital, which is supported by The Ottawa Hospital Foundation and its donors.
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AB, GL, AA, JC, JH, NA, LV, GP, and MC designed the survey and prepared the protocol. LV collected the data and coordinated the study. GP did the statistical analysis. AB wrote the manuscript. All authors had full access to the data and took responsibility for the integrity of the data and accuracy of the data analysis. All authors were involved in the critical review of the manuscript and approved the final version.
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This study was approved by the Ontario Cancer Research Ethics Board (OCREB).
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Beltran-Bless, AA., Larocque, G., Brackstone, M. et al. The COVID-19 pandemic and its effects on follow-up of patients with early breast cancer: A patient survey. Breast Cancer Res Treat 204, 531–538 (2024). https://doi.org/10.1007/s10549-023-07232-3
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DOI: https://doi.org/10.1007/s10549-023-07232-3