Oncology

Cancer: fewer deaths, but in Italia there is a 15-month wait for new medicines

In Europe, the estimated number of new cases stands at 2.7 million per year, but thanks to innovation, deaths have fallen to 1.2 million, with a 7.8 per cent decrease among men and a 5.9 per cent decrease among women

5' min read

Translated by AI
Versione italiana

5' min read

Translated by AI
Versione italiana

Every year in Europe, there are 2.7 million new cases of cancer, equivalent to 5 every minute. On the other hand, thanks to prevention campaigns and increasingly effective treatments, around 7.3 million cancer-related deaths have been prevented in the European Union since 1988. In 2026, an estimated 1,230,000 people will die from cancer, representing a decrease of 7.8 per cent for men and 5.9 per cent for women compared with the period 2020–2022.

The benefits of innovation

Lung cancer in men has seen the most significant decline (-22.5 per cent). Innovation does not merely translate into lives saved, but also into the opportunity to reintegrate people who have experienced cancer back into society and the workforce. In Europe, in fact, indirect costs – linked primarily to the loss of productivity caused by the disease – have fallen by 16 per cent over approximately 30 years, from €97 billion in 1995 to €82 billion in 2023.

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Barriers to accessing healthcare

However, there are still issues regarding access to innovative treatments. In Europe, in fact, on average only 51 per cent of new medicines approved by the European Medicines Agency (EMA) are made available, and it takes 655 days to gain access to them (in 2025). Italia’s figures are better, although the waiting times are still too long. Italia guarantees access to 89 per cent of the anti-cancer drugs approved by the EMA and, in this ranking, comes second in Europe after Germany (91 per cent) (Austria 86 per cent; Spain 73 per cent; France 68 per cent). In Italy, however, it takes 470 days – or around 15 months – for new treatments to become available. The call to speed up these timescales comes from the Italian Association of Medical Oncology (Aiom), at the scientific society’s official press conference at the Congress of the European Society for Medical Oncology (ESMO), which opens today in Madrid.

The AIOM’s appeal

“The decline in smoking amongst men is the reason behind the greater reduction in cancer mortality amongst the male population, and this trend is also evident in Italia,” explains Massimo Di Maio, President of Aiom. “Innovative treatments not only improve survival rates, but also facilitate a return to work and social life. The reduction in the indirect costs of cancer is a very significant achievement, driven by increasingly effective treatments, which must be available to all patients if we are to speak of equity in innovation. Over the course of a year, the time taken to access new anti-cancer drugs has increased by more than two months in Europe and by around one month in Italia. In 2024, it took an average of 586 days in Europe and 441 days in Italia. In Italia, critical issues remain regarding bureaucratic and administrative procedures because, following approval of reimbursement by the Italian Medicines Agency, in some regions it is necessary to wait for the drugs to be included in the Regional Therapeutic Formulary. Further delays may be caused by regional tendering processes and the need for inclusion in Hospital Therapeutic Formulary lists as well. For many years, AIOM has been highlighting regional and local delays in the provision of medicines. Immediate availability must be ensured following publication in the Official Gazette.”

The effects of the US MFN

The time it takes to access new treatments could be further delayed due to the ‘Most Favoured Nation’ (MFN) clause, established by the US administration, which aims to reduce the prices of American medicines by bringing them into line with the lower prices in other countries, including Italia. ‘This measure,’ continues Massimo Di Maio, ‘risks further prolonging waiting times and having serious repercussions on cancer care in our country. Pharmaceutical companies, in fact, might decide to delay the launch of new innovative cancer therapies in Europe and Italia, or not make them available at all, to prevent a low local price from affecting or reducing revenues in the more profitable US market.”

Spending: Italia third in the EU

Over a 10-year period (2014–2023), spending on anti-cancer drugs in Europe rose from 24.9 billion euros to 64.3 billion. This growth was driven by a combination of price-related factors and an increase in the number of cancer cases. Italia accounts for 14 per cent of European spending on cancer medicines and ranks third after Germany (19 per cent) and France (19 per cent). ‘In Europe, the share of chemotherapy in total expenditure on cancer drugs has fallen from 22 per cent in 2014 to 6 per cent in 2023, overtaken by targeted therapies and immunotherapies,’ says Giuseppe Curigliano, President-elect of ESMO. Immunotherapies alone now account for 29 per cent of expenditure. These changes reflect the growing impact of precision oncology, which enables the selection of the most suitable treatment for each individual patient. The number of approvals by the EMA has increased significantly, rising from an average of one new medicine per year between 1995 and 2000 to around 14 per year between 2021 and 2024. Western European countries tend to reimburse a greater number of therapies and to do so more quickly than in Central and Eastern Europe. For example, Germany made 91 per cent of the cancer medicines approved by the EMA in the period 2021–2024 available within just over 100 days, whilst Romania, Estonia, Malta, Slovakia and Latvia, the figure stands at 20 per cent or less, and the reimbursement time is around 1,000 days in Lithuania, Romania and Estonia, resulting in significant inequalities that must be addressed as soon as possible.”

The role of Molecular Tumour Boards

“Biomarker testing has now become a cornerstone of precision medicine, as it enables us to identify the most appropriate treatment for each individual patient,” explains Rossana Berardi, President-elect of AIOM. Technologies such as next-generation sequencing enable the simultaneous analysis of many molecular alterations, but the complexity of the results makes the role of Molecular Tumour Boards increasingly important; they are essential for translating genomic data into appropriate clinical decisions. Italia has a highly valued National Health Service, competitive clinical research and a unique wealth of real-world data, thanks in part to the AIFA monitoring registers. These are resources we must make the most of to attract research, clinical trials and investment. Supporting Italian oncology means not only ensuring better care for patients today, but also helping to generate, right here, the innovation and evidence that will guide the treatments of tomorrow.’

Investing in research and prevention

It is estimated that 5 per cent of the population in Europe has been diagnosed with cancer, amounting to a total of 23.7 million people. “There are 4 million people living in Italia following a cancer diagnosis,” concludes President Di Maio. “In 2025, an estimated 390,000 new cases are expected in our country. Survival and recovery rates are rising for many types of cancer. Sixty-three per cent of women and 54 per cent of men are still alive after five years, and at least one in four patients has regained the same life expectancy as the general population and can be considered cured. To further improve these outcomes, it is essential to invest in research and prevention programmes.”

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