The coordination of cancer care for Indigenous Australians has been recognised as critical in addressing Indigenous patients' needs, for example in relation to navigating the health system, providing essential information and communication and ensuring cultural safety [1]. However, challenges to the provision of coordinated care to meet Indigenous cancer patients needs include: lack of communication between services; delays in receiving timely hospital information; language and cultural barriers; distance to treatment; as well as providing cultural support and having hospital facilities that accommodate extended families [1-4]. These challenges often stem from health system design, structures and limitations [1]. Quality cancer care for Indigenous Australians as defined by the National Aboriginal and Torres Strait Islander Cancer Framework is evidence-based, personcentred (incorporating the family and cultural roles) [5, 6], timely, equitable and delivered as close to home as safely as possible [5, 7, 8]. It is also multidisciplinary, integrated across the health sector (primary, secondary and tertiary), embedded within the community [5, 9] and also involves strong involvement and leadership from the Indigenous community [5, 10]. Pathways for accessing cancer care for Indigenous Australians can be more complex than for other Australians, with additional challenges for them relating to culture, language, and lack of familiarity with navigating services and institutions in the wider health care system [11]. Besides coming to terms with a cancer diagnosis,