Sundheds- og Ældreministeriet
Enhed: SPOLD
Sagsbeh.: DEPAJU
Koordineret med:
Sagsnr.: 2001466
Dok. nr.: 1290242
Dato: 31-07-2020
NOTAT
Denmark’s position on the ”Europe’s Beating Cancer Plan”
Inequality in cancer incidence and survival
Lower socioeconomic and vulnerable groups have higher morbidity and mortality of
cancer statistically. These groups have lower health literacy, are less aware of cancer alert
symptoms, are less likely to seek medical attention when having symptoms of cancer, and
they participate less in cancer screening programs. The social gradient is present
throughout the entire cancer care pathway in the form of differences in incidence,
diagnosis and treatment, late treatment complications, occupational attachment and
survival.
Reduced inequality within and among countries is one of the United Nations’ Sustainable
Development Goals (SDG 10). Reducing inequality in health is also a key priority for the
Danish government, and Denmark therefore advocates that the “Europe’s Beating Cancer
Plan” should have a broad focus on fighting inequality in health by encompassing
initiatives to even out the social gradient in cancer incidence and survival within each of
the four pillars of the Plan. Citizens have different backgrounds and their preconditions for
using health care are therefore not the same. Denmark advocates that the Cancer Plan
contains initiatives that focus on increasing health literacy and making health care more
accessible for lower socioeconomic population and vulnerable groups.
Knowledge, data and scientific evidence
In recent years, we have gained more knowledge about risk factors for cancer and
effective treatment. There is still a 'knowledge gap', especially in terms of follow-up and
life as a cancer survivor. Denmark supports a partnership and cooperation between EU
member countries on data collection and knowledge exchange in the field of cancer.
It is a Danish priority in the field of cancer to support actions and initiatives to promote
knowledge, data and scientific evidence for example:
Initiatives to develop a cancer knowledge centre whose main task is to promote
cancer treatment, collect evidence and develop guidelines for clinical diagnosis
and treatment practices.
Initiatives for a European clinical quality database covering all cancers that
collects data from all countries and provides epidemiological support to a cancer
knowledge centre.
Development and research into new technologies within medical and digital
welfare solutions as these tools are important in order to meet diverse health
needs within different patient groups. Furthermore, individualised medicines, to
disseminate specialized treatment services, to support medical decision-making,
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