“…There is not enough knowledge about screening investigations (what, when and why are they necessary), and survivors report fewer contacts with experts in the field e 'don't know where to go', 'lost in follow-up' [25,26]. Nowadays, most paediatric oncologists ensure that adequate information on treatments, risks and prevention opportunities is provided to all CCS at the end of treatment and again at the time of transition to adult care [10,11]. It should, however, be recognised that the impact of the delivery of care plans in the posttreatment period still needs to be further assessed.…”