“…A recent systematic review of self-reported CRCI measures noted that this research has predominantly but not exclusively involved women with breast cancer, and that such self-report measures tend to show moderate to strong relationships with other patient-reported outcomes but weak or absent associations with neuropsychological tests (Bray et al, 2018). People affected by CRCI have emphasised its impact on quality of life (Tannock et al, 2004) due to limitations in activities such as work performance (Boykoff et al, 2009;Myers, 2013;Von Ah et al, 2013;Wagner et al, 2009), and family and social life (Green et al, 2019). Many researchers have found increases in selfreported CRCI to associate with increased psychological distress and fatigue (King & Green, 2015;Lai et al, 2009;Vardy & Dhillon, 2017); these bidirectional relationships indicate that it is important to consider broader function, such as emotional and physical wellbeing, in addition to neurological functioning (Costa et al, 2018;Green et al, 2005;Skaali et al, 2011).…”