The solitary versus supported experience: Care inequality between rare and common cancer patients

Abstract Objective Patients with a rare cancer (RC) often have a more complex disease trajectory than patients with a common cancer. Research involving both patient groups is needed to identify differences and resemblances. In this study, we aimed to explore and compare experiences, needs and quality of life of patients with rare and common cancer throughout the disease trajectory. Methods A qualitative focus group study was conducted, including patients with rare and common cancer ( n = 25). Participants were purposively selected to reflect heterogeneity of cancer types. A semi‐structured topic list was used. Focus groups ( n = 4) were recorded, transcribed verbatim and analysed, using thematic analysis. Results Three themes were identified emphasizing care inequality between patients with rare and common cancer: (1) The solitary experience: lack of information and support impact the RC patient, (2) Sudden impact, but recognition reduces the common cancer burden, and (3) Absence of psychosocial care requires being empowered as a cancer patient. Conclusions Patients with RC are faced with enormous challenges due to the high impact of their solitary experience on their quality of life, while patients with common cancer generally experience social support and recognition alleviating their burden. Centralisation of care for patients with RC is needed and tailored psychosocial care should be provided to overcome inequalities.