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Annalisa Trama

Head of Evaluative Epidemiology Unit
Fondazione IRCCS Istituto Nazionale dei Tumori
Participates in 2 items

Annalisa Trama is the Director of the Evaluative Epidemiology Unit at the Fondazione IRCCS Istituto Nazionale Tumori (INT), Milan, Italy.

Her research activities focus on rare cancers and adolescent and young adult cancers. She is an expert in population-based research including population-based cancer registries and administrative datasets. She was a founder of RARECARE (surveillance of rare cancers in Europe) which proposed a definition for rare cancer. She was the founder of RARECAREnet Asia, a collaboration between European and Asian population-based cancer registries (CRs) on rare cancers. In the area of rare cancers, she co-coordinated the Joint Action on Rare Cancers (JARC), carried out between 2016 and 2019 within the framework of the Third Health Programme of the European Union (EU) with 34 partners and 18 EU Member States. She coordinates the clinical registry of EURACAN, the European Reference Network on rare adult solid cancers. She was a founder of the first Italian adolescent and young (AYA) cancer survivor cohort and she coordinate the Steering committee of this cohort. She is a member of the Scientific Coordination of EUROCARE (surveillance of cancer patients in Europe). She is PI of national and international projects exploiting secondary use of real-world data (e.g. electronic health record, administrative database, clinical registries, population-based registries) and use of innovative solutions (e.g. data fusion; AI approach for defining causal relationship; AI solution to support interoperability of data sources).

She is (co)author of more than 100 papers in peer-reviewed medical journals.

Sessions in which Annalisa Trama participates

quinta-feira 15 maio, 2025

Time Zone: (GMT+01:00) Paris
11:00
11:00 - 12:15 | 1 hour 15 minutes
Health and Medical Data Compliance
Regulatory evolutionData regulation in practiceInterpretation available

In pursuit of medical breakthroughs, data is considered a goldmine. At the same time, accessing medical data should not come at the expense of crossing legal and ethical lines. This session will tackle one of the most important issues in medical research today: the lawful use of patient data for secondary purposes like advancing scientific discovery and healthcare innovation. The distinguished panel of this session will explore the complex questi...

sexta-feira 16 maio, 2025

Time Zone: (GMT+01:00) Paris
11:00
11:00 - 13:00 | 2 hours
Accountability, Trust and PET
Regulatory evolutionHealth and medical data Data regulation in practiceDeep dive in and capacity buildingInterpretation available

Imagine a future in which medical research, innovation, and patient care seamlessly benefit from secure data sharing across Europe. European Health Data Spaces are designed to make this vision a reality, but how do they work in practice? This session goes beyond policy and legal frameworks to explore the real-world implementation of European Health Data Spaces and what they mean for future healthcare innovation.