Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8442224 | European Journal of Cancer | 2015 | 10 Pages |
Abstract
Registration of PROCARE patient data was incomplete, biased and variable between centres. Participation on a voluntary basis should be avoided for further projects. Quality assurance on a centre level requires compulsory and complete registration with a minimal but relevant data set for all patients treated in all centres.
Related Topics
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Biochemistry, Genetics and Molecular Biology
Cancer Research
Authors
D. Jegou, F. Penninckx, T. Vandendael, C. Bertrand, E. Van Eycken, PROCARE PROCARE,