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For the most part, data limitations hinder the ability to provide comprehensive evidence because most studies used registries collected at a single hospital (Davis et al. 2013; Dixon et al. 2014; Kondo et al. 2011; Kwan et al. 2011; McCoy et al. 2013).
Provincial cancer registries collected information from sampled controls using the same protocol as for the cases.
The provincial registries collected data by self-administered questionnaires, with telephone follow-up when necessary for clarification and completeness.
Between 1 January 1995 and 31 December 1995, the six French local registries collected 1535 cases of colorectal cancer.
Risk of ER/PR-defined tumours was evaluated using data only from participants that lived in states where registries collected hormone receptor data.
All these cancer registries collected skin cancers routinely (Parkin et al, 2002), with the exception of Murcia and Montpellier which did not cover BCC.
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Population-based cancer registries collect data that enable the estimation of cancer survival.
National registries collect this data, producing research opportunities, outcome standards and a means by which to benchmark trauma centre performance.
The registries collect data from cancer patients automatically, although patients can object to their details being shared.
SEER registries collect cancer incidence information according to high-quality and rigorous standards [ 52].
Since these registries collect data in a prospective and consistent manner, information bias is minimized.
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