Data from Population-based Cancer Registration for Secondary Data Analysis: Methodological Challenges and Perspectives

Arndt, V; Holleczek, B; Kajüter, H; Luttmann, S; Nennecke, A; Zeissig, S.R; Kraywinkel, K; Katalinic, A

doi:10.1055/a-1009-6466

CareLit Fachartikel

Data from Population-based Cancer Registration for Secondary Data Analysis: Methodological Challenges and Perspectives

Arndt, V.; Holleczek, B.; Kajüter, H.; Luttmann, S.; Nennecke, A.; Zeissig, S.R.; Kraywinkel, K.; Katalinic, A. · Das Gesundheitswesen · 2019 · Heft S 01 · S. S62 bis S71

Dokument

575744

CareLit-ID

Jahr

2019

Publikation

PDF

ja

Volltext

DOI

ja

zitierfähig

Bibliografische Angaben

Zeitschrift

Das Gesundheitswesen

Autor:innen

Arndt, V.; Holleczek, B.; Kajüter, H.; Luttmann, S.; Nennecke, A.; Zeissig, S.R.; Kraywinkel, K.; Katalinic, A.

Ausgabe

Heft S 01 / 2019

Jahrgang 81

Seiten

S62 bis S71

Erschienen: 2019-10-29 13:00:00

ISSN

0941-3790

DOI

10.1055/a-1009-6466

Zusammenfassung

Population-based cancer registries have a long-standing role in cancer monitoring. Scientific use of cancer registry data is one important purpose of cancer registration, but use of cancer registry data is not restricted to cancer registries. Cancer registration in Germany is currently heading towards population-based collection of detailed clinical data. This development together with additional options for record linkage and long-term follow-up will offer new opportunities for health services and outcome research. Both regional population-based registries and the German Centre for Cancer Registry Data (ZfKD) a…