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Characteristics of cohorts in the Childhood Cancer Research Group

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Characteristics of cohorts in the Childhood Cancer Research Group at the Danish Cancer Society’s Research Center

Cohort name (acronym) Adult Life after Childhood Cancer in Scandinavia - ALiCCS Main focus areas Somatic late effects in all organs and organ systems after

treatment for childhood cancer Source of identification of

study population

Nordic cancer registries and central population registries

Study population 33,160 1-year survivors of childhood cancer from Denmark, Finland, Iceland, Norway and Sweden diagnosed at age 0- 19 years between 1943-2008 and five as many randomly selected population comparisons individually matched Design and data collection

Study design Cohort and case-cohort studies

Setting Population-based

Data sources (yes/no)

Registers Yes

Medical records Yes

Questionnaires No

Interviews No

Physical examinations No Bio samples (if yes,

specify)

No

Other tests No

Website and/or contact person and link to cohort design paper

www.aliccs.org

Jeanette Falck Winther, jeanette@cancer.dk

https://onlinelibrary.wiley.com/doi/full/10.1002/pbc.25661

Referencer

RELATEREDE DOKUMENTER

The studies were based on the unique Adult Life after Childhood Cancer in Scandinavia (ALiCCS) cohort including all children with cancer diagnosed in the Nordic

Since 2016, ten national research centres have been established within the following fields: childhood cancer, circulating tumour DNA guided treatment, equity in cancer,

Since 2016, ten national research centres have been established within the following fields: childhood cancer, circulating tumour DNA guided treatment, equity in cancer,

Before starting analyses for this study and linking study subjects to the hospital registers, we have excluded those in whom more than one primary cancer was diagnosed in childhood

Signe Sloth Mogensen, Copenhagen University Hospital, Rigshospitalet, Denmark Skeletal late effects in childhood cancer survivors – ALiCCS cohort study. Trausti Oskarsson,

The Nordic Cancer Union (NCU) consisting of the national cancer societies in the Nordic countries, invites research institutions to submit research proposals on Covid-19 and

Main focus areas Socioeconomic circumstances and family factors in long- term survivors after childhood cancer, while also. considering the somatic and psychiatric disease burden

Patients and methods: The study cohort consists of 5-year survivors of childhood cancer treated at VU University Medical Center for any type of cancer and an age-matched group