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Breast cancer screening based on individual risk characteristics
Summary
The following activities will be carried out: survey of existing, ongoing, and planned risk assessment experimentations and evaluation of their impact on benefits; review of guidelines and identification of research gaps and implementation, and prioritised clinical questions for guideline updates; systematic review and multidisciplinary
analysis (consensus method) of cost-effectiveness models and socio-psychological impact, and Patient Reported Outcomes (PROMS); collection and analysis of data on feasibility, transferability, and challenges in different screening approaches; and development of a toolbox for critical analysis of screening strategies to support decision makers at national/local level (expected benefits, costs, cost-effectiveness).
This task will be led by Unicancer, France, co-led by CPO, Italy.
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Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or European Health and Digital Executive Agency (HADEA). Neither the European Union nor HADEA can be held responsible for them.
The general objective of EUCanScreen is to assure sustainable implementation of high-quality screening for breast, cervical and colorectal cancers, as well as implementation of the recently recommended screening programs – for lung, prostate and gastric cancers. EUCanScreen will facilitate the reduction of cancer burden and achieving equity across the EU.
This project has received funding from the European Union’s EU4HEALTH Programme under the Grant Agreement no 101162959
