Acute myeloid leukaemia: the value of treatment is also measured in terms of the time gained
The challenge lies in translating these analyses into concrete decisions: negotiations on the price of a treatment and on budgets are the stages where the timing must be right
Key points
For years, in the healthcare sector, the main constraint has been money. Today, people’s time is also a constraint, and the figures bear this out: in 2024, 9.9 per cent of Italians went without a healthcare service they needed, and the most common reason was not the cost but excessively long waiting times (Istat, Annual Report 2025).
Whenever a treatment helps to buy time, that time becomes valuable. For the patient, who can reclaim days to devote to their daily life; for the carer, who can reduce the hours spent providing care; for the healthcare facility, which can free up resources and care capacity; and for the system as a whole, which can improve the organisation of services and the use of available resources.
Yet, when assessing innovation in healthcare, time often remains an implicit factor, secondary to clinical outcomes and traditional economic indicators. This is a perspective that deserves to be re-examined, particularly in a context where the sustainability of healthcare systems depends not only on financial resources, but also on the ability to organise and make the best use of the time of healthcare professionals, patients and their families. Time, in fact, is not a secondary resource in relation to care. It is a component of its quality and, increasingly, a dimension through which to measure the value of innovation.
These issues were recently discussed in Bologna at the press conference entitled ‘LMA: A Future in the Present – How Innovation is Transforming the Management of Acute Myeloid Leukaemia’, held at Palazzo Pepoli.
The value of care
If time, therefore, becomes a measure of the quality of care, the way in which we assess innovation also changes. Alongside clinical outcomes, we must take into account the time required for care pathways, the resources used and the organisational burden borne by patients, carers and the healthcare system.

