Data & Evidence

The case for equal access to cancer trials isn't just emotional — it's backed by hard data. Here's what the evidence shows.

Cancer Burden in the EU

This section covers the scale of cancer across the EU today — how often it's diagnosed, who it affects, and how the burden is projected to grow if nothing changes.

30% / 25%

lifetime risk of being diagnosed with cancer before age 74 for men / women, EU-wide, based on 2024 estimates

23.9%

share of all EU deaths in 2023. Without further progress in prevention, early detection, and treatment, cancer could become Europe's leading cause of death by 2035.

Five people are diagnosed with cancer every minute in Europe

3.7 million new cases and 1.9 million deaths per year, making cancer the second-leading cause of death in Europe after cardiovascular disease.

~1.28 million cancer deaths projected for the EU in 2025
Lifetime risk ranges from 16% (Albania) to 33% (Norway/Denmark)

Risk of dying ranges from 8% (Switzerland) to 16% (Hungary) — geographic inequality even before trials enter the picture.

2024 EU-27 data show substantial variation

Northern and Western Europe generally have higher incidence, while Central and Eastern Europe show the highest mortality rates.

The Funding Gap

<€150 vs >€400

Hungary, Croatia, Romania, Latvia and Bulgaria spend under €150 per capita on cancer care annually; Germany and Switzerland spend over €400 — nearly a three-fold gap, and higher spending is associated with higher survival.

Stable share of healthcare spend

Cancer care has held a stable share of total healthcare expenditure over the last decades, despite a growing number of cases.

The Accessibility Gap

Including new treatment options and clinical trials

<100 vs 900 days

Germany reimbursed nearly all cancer medicines with EMA approval from 2019–2022 within 100 days. Malta, Estonia, Slovakia and Romania reimbursed fewer than 20% of new medicines, and average time to reimbursement in Latvia and Lithuania was close to 900 days.

Uneven diagnostic access

Molecular diagnostics are vital for precision oncology, but access remains limited, especially in Central and Eastern European countries, where testing infrastructure lags behind Western Europe.

30% vs. 11%

Share of eligible large B-cell lymphoma (LBCL) patients receiving CAR T-cell therapy, France vs. Italy (2023) — access varies sharply across major European countries.

The Survival Gap

~200,000

Cancer deaths that could be avoided each year across Europe if more countries achieved survival rates similar to Sweden's.

1.6x / 37%

Cancer mortality rates vary 1.6-fold across EU countries, and by up to 37% between regions within a single country.

References
02 — EU vs World

EU vs World

This section compares clinical trial capacity between the EU and the rest of the world, covering Europe's shrinking share of global trials, the oncology-specific gap with the US, the next frontier in cell and gene therapy, and what's driving the divergence.

Europe's shrinking share

22% → 12%

EU global trial share, 2013–2023

60,000

fewer trial places for Europeans

Global clinical trial activity grew 38% over the last decade. Europe's share of it fell by almost half.

Source EFPIA

This is the gap our proposed Cancer Clinical Trials Fund is built to close: enabling genuine cross-border access so a patient's postcode doesn't decide whether they can enroll, and backing the harmonisation Europe needs to compete again for the trials that save lives.

03 — Economics

The Economics of Inaction

This section lays out the real cost of cancer to European health systems and economies — including annual healthcare costs, lost workforce productivity, and the case for treating clinical trial investment as cost-saving rather than an added expense.

The scale of the cost

+43%

1995–2023

rise in cancer's combined direct and indirect cost across Europe between 1995 and 2023, from €159 billion to €228 billion (2023 prices)

€1.3 trillion

2018–2040 projection

projected lost labour productivity from cancer-related premature mortality between 2018 and 2040 — an average of €58.7 billion a year, or 0.43% of EU-27 GDP, every year, for two decades

Inequality shows up in the cost data too

Bulgaria / Romania ~€150
Switzerland €1,011

Cost per cancer case varies sevenfold across Europe — from around €150 in Bulgaria and Romania to €1,011 in Switzerland (2023). That gap has narrowed from twelvefold in 1995, but it's still stark evidence that where you get sick still determines what gets spent trying to save you.

Figures shown are the lowest and highest reported values across 31 European countries in the source study, not the full country-by-country range.

The case for research as cost-saving, not just cost

NCI's trial network: 14.2 million life-years at $326 each

On the US side, NCI's own trials network shows what return on investment looks like: since 1980, its publicly funded trials have generated an estimated 14.2 million additional life-years for cancer patients, at a federal cost of just $326 per life-year gained — one of the most cost-effective public health investments on record. For context, standard health-economics cost-effectiveness thresholds run $50,000–$150,000 per quality-adjusted life-year, per ICER's (Institute for Clinical and Economic Review) value assessment framework — making the NCTN's $326 figure an order of magnitude below typical benchmarks, though the two aren't directly equivalent units. Set against a €228 billion annual EU cost base, even modest gains in survival or earlier access translate into large productivity recoveries — the trials themselves are cheap relative to what cancer already costs the EU economy every year.

The European Cancer Clinical Trials Fund isn't competing against existing costs — it's a comparatively small, high-leverage investment set against a €97B/year health cost and €50B/year productivity loss that's already being paid, with or without the Fund.

References
04 — Clinical Trials

Clinical Trial Access

This section covers the EU's current clinical trials regulatory system (CTR/CTIS), recent efforts to speed up trial approvals, and why none of that yet guarantees a patient can actually reach a trial that exists elsewhere in the EU.

41% → 21%

EU's share of global oncology clinical trials, 2008–2023 — a near-halving of relative research capacity in 15 years

Source EFPIA

~0.75 Gini index

for clinical trial access across global income tiers — comparable to some of the world's most unequal income distributions, applied instead to trial access

Source NIH
Access to clinical trials remains unequal across the EU

Significant disparities particularly affect Eastern and Southeastern EU countries, and lung cancer trials are primarily concentrated in Western Europe.

48% of lung cancer patients feel inadequately informed

A 2022 Lung Cancer Europe survey found this — access is a discovery problem as well as a geographic one.

The current regulatory architecture (CTR/CTIS)

CTR (EU 536/2014) fully in force since 31 January 2025

The transitional period from the old Clinical Trials Directive ended on this date. All active trials must now run through the Clinical Trials Information System (CTIS) — a single EU-wide submission portal replacing parallel national applications.

~200 new clinical trial applications submitted per month via CTIS

Around 80 of those (roughly 40%) are multinational — evidence that sponsors are actively using the single-portal model where cross-border trials are cheaper to run.

13,700+ applications received, 11,100+ trials authorised

Since 2022, through CTIS — 13,778 submissions and 11,183 authorisations as of Q1 2026.

CTIS became a WHO Primary Registry in April 2025

Making EU trials fully discoverable through the WHO's global trial platform. Designated a member of the Primary Registry Network of ICTRP on 3 April 2025.

Patient-facing "Trial Map" launched March 2025

Lets patients and clinicians search live trials by condition and geography through the CTIS Public Portal, available in 26 EU languages — a first step toward connecting patients to trials, though it depends entirely on trials existing to find.

Recent acceleration efforts

FAST-EU: 70-day (10-week) max timeline

A voluntary one-year pilot agreed 27 November 2025 and launched 30 January 2026, guaranteeing a maximum 70 calendar days end-to-end, from CTIS submission to decision, for multinational trial authorisation.

European Biotech Act: 106 days → 75 days

Proposed 16 December 2025, cutting initial approval timelines from around 106 days to 75 days, and down to as little as 47 days for straightforward applications.

"Choose Europe for Life Sciences" strategy, July 2025

Sets an explicit ambition for the EU to be the world's most attractive life sciences location by 2030.

The direction is right, but still procedural: FAST-EU is a voluntary one-year pilot, the Biotech Act is still a proposal working through the legislative process, and even the Commission's own strategy stops at ambition — not a dedicated funding line for rare cancer trials.

The gap this section sets up: CTIS, FAST-EU, the Biotech Act make it faster and cheaper to authorise a trial a sponsor already chose to run in the EU. None of it addresses where sponsors choose to run trials in the first place, or guarantees a patient in a country with no open trial can enroll in one elsewhere. Procedural streamlining hasn't reversed the EEA's shrinking share of global trials (12% in 2023, down from 22% in 2013) — because the barrier isn't paperwork speed, it's where trial capacity and funding are sited.

References
05 — Rare Cancers

Rare Cancers — What Exists, What's Missing

This section covers the scale of the rare cancer burden across the EU, the cross-border infrastructure that already exists (like the European Reference Networks), and why rare cancers make the sharpest case for a dedicated trials fund.

~5.1 million

people across the EU and UK affected by rare cancers (incidence under 6 per 100,000/year), 650,000+ new cases annually

Source IARC

~22–24%

share of all cancer diagnoses that are rare cancers, collectively — not a small policy problem

Source IARC
Rare cancers 47%
Common cancers 65%

Five-year survival — an 18-point gap driven largely by delayed diagnosis, fewer expert centres, and fewer trial options, not biology alone.

What exists — and where it breaks down

The EU already built the infrastructure: European Reference Networks (ERNs) link specialist centres in all 27 countries into disease-specific networks — EURACAN for rare adult solid cancers, EuroBloodNet for rare blood cancers — solving the problem that no single country has enough rare cancer patients to sustain expert care alone. Orphan drug rules add real incentives on top: up to 10 years of market exclusivity, faster review, and fee waivers.

What's missing is money to run it. ERNs were never funded to do the cross-border trial-matching work they exist for — and it shows: only 5–6% of rare diseases have a dedicated treatment, and patients still face delays, fewer trials, and worse outcomes than the infrastructure was built to prevent.

Why this is the sharpest case for the Fund: Rare cancers are the textbook example of the Gap Analysis argument — no single Member State has enough patients to power a trial alone, ERNs already provide the cross-border clinical infrastructure to pool them, but there's no dedicated funding mechanism to actually run the trials once patients are pooled. The Fund would complete a chain EURACAN and EuroBloodNet can't finish alone.

References