Abstract
BACKGROUND: The unmet post-treatment needs and issues of cancer survivors for follow-up care are still significant, matching appropriate and acceptable follow-up care to cancer survivors' preferences, may increase adherence of survivors to health programs and quality of life. There is a knowledge gap about how cancer survivors measured their choices between different aspects of follow-up care. As discrete choice experiments (DCE) have been widely used in patient preference elicitation, we reviewed DCE on follow-up care for cancer survivors. METHODS: The electronic databases PubMed, The Cochrane Library, Embase, and Web of Science were searched, up to October 06, 2024. Original studies reporting preferences of cancer survivors for follow-up care elicited by DCE were eligible. Findings were presented using a narrative synthesis. Using two validated checklists to evaluate the quality of the included DCE studies. RESULTS: A total of 3525 records were identified and 9 papers were included. The studies were conducted in the Netherlands, Australia, the United Kingdom (UK) and China with 123 to 722 participants evaluated preferences of cancer survivors for follow-up care. Most of included cancer survivors were after completed the main treatment. Several key attributes for cancer survivors' follow-up care were identified including healthcare provider, services offered, frequency of visits, contact mode, familiarity of healthcare provider with patients' medical history/continuity of care. CONCLUSIONS: The systematic review focusing on preferences of cancer survivors follow-up care and attributes identified in these studies, the results may inform healthcare providers should take cancer survivors preferences into account.