Objectives: This study aims to explore older adults’ perceptions of priorities for research in cancer and haematological malignancies, and propose an agenda of patient-driven priorities for cancer care research in the field of geriatric oncology. Data Sources: Sixteen older adults (≥65 years) living with or after a diagnosis of cancer participated in a descriptive qualitative study. Participants were purposively recruited via a regional cancer centre and cancer advocacy organisations. Semi-structured telephone interviews explored participants’ experiences of cancer, and perceptions of priorities for future cancer-related research. Conclusions: Participants reported positive experiences of cancer care. However, positive and negative experiences of information, symptoms, and support both within and beyond the hospital setting were highlighted. Forty-two research priorities in six thematic areas were identified: 1) recognition of the signs and symptoms of cancer; 2) research about cancer treatment; 3) assessment and management of co-morbidities; 4) unmet needs of older adults living with and after cancer; 5) impact of COVID-19; and 6) impact on caregivers and family members of people living with and after cancer. Implications for Nursing Practice: The results of this study provide a basis for future priority-setting activities which are culturally and contextually sensitive to the healthcare systems, resources and needs of older adults living with and after cancer. Based on the findings of this study, we make recommendations for the development of interventions which can build awareness, capacity, and competence in geriatric oncology among cancer care professionals, and consideration of the diverse needs of older adults in the development of interventions to address unmet information and supportive care needs.
【저자키워드】 Older adults, Cancer, frailty, Qualitative, Unmet Needs, Research Priorities,