International Journal of Cancer

Volume 132, Issue 12
Epidemiology

Availability of stage at diagnosis, cancer treatment delay and compliance with cancer guidelines as cancer registry indicators for cancer care in Europe: Results of EUROCHIP‐3 survey

Sabine Siesling

Corresponding Author

E-mail address: s.siesling@iknl.nl

Department of Research, Comprehensive Cancer Centre the Netherlands, Utrecht, The Netherlands

Department of Health Technology and Services Research, Twente University, Enschede, The Netherlands

Department of Research, Comprehensive Cancer Centre the Netherlands, P.O. Box 19079, 3501 DB Utrecht, The NetherlandsSearch for more papers by this author
Annemiek Kwast

Department of Research, Comprehensive Cancer Centre the Netherlands, Utrecht, The Netherlands

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Anna Gavin

Northern Ireland Cancer Registry, Queens University, Belfast, Northern Ireland, United Kingdom

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Paolo Baili

Descriptive Studies and Health Planning Unit, Fondazione IRCCS “Istituto Nazionale dei Tumori,” Milan, Italy

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Renee Otter

Department of Research, Comprehensive Cancer Centre the Netherlands, Utrecht, The Netherlands

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First published: 26 November 2012
Cited by: 14

Abstract

EUROCHIP (European Cancer Health Indicators Project) focuses on understanding inequalities in the cancer burden, care and survival by the indicators “stage at diagnosis,” “cancer treatment delay” and “compliance with cancer guidelines” as the most important indicators. Our study aims at providing insight in whether cancer registries collect well‐defined variables to determine these indicators in a comparative way. Eighty‐six general European population‐based cancer registries (PBCR) from 32 countries responded to the questionnaire, which was developed by EUROCHIP in collaboration with ENCR (European Network of Cancer Registries) and EUROCOURSE. Only 15% of all the PBCR in EU had all three indicators available. The indicator “stage at diagnosis” was gathered for at least one cancer site by 81% (using TNM in 39%). Variables for the indicator “cancer treatment delay” were collected by 37%. Availability of type of treatment (30%), surgery date (36%), starting date of radiotherapy (26%) and starting date of chemotherapy (23%) resulted in 15% of the PBCRs to be able to gather the indicator “compliance to guidelines”. Lack of data source access and qualified staff were the major reasons for not collecting all the variables. In conclusion, based on self‐reporting, a few of the participating PBCRs had data available which could be used for clinical audits, evaluation of cancer care projects, survival and for monitoring national cancer control strategies. Extra efforts should be made to improve this very efficient tool to compare cancer burden and the effects of the national cancer plans over Europe and to learn from each other.

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