Reporting of prognostic markers: current problems and development of guidelines for evidence-based practice in the future
Open Access
- 15 April 2003
- journal article
- Published by Springer Nature in British Journal of Cancer
- Vol. 88 (8) , 1191-1198
- https://doi.org/10.1038/sj.bjc.6600886
Abstract
Prognostic markers help to stratify patients for treatment by identifying patients with different risks of outcome (e.g. recurrence of disease), and are important tools in the management of cancer and many other diseases. Systematic review and meta-analytical approaches to identifying the most valuable prognostic markers are needed because (sometimes conflicting) evidence relating to markers is often published across a number of studies. To investigate the practicality of this approach, an empirical investigation of a systematic review of tumour markers for neuroblastoma was performed; 260 studies of prognostic markers were identified, which considered 130 different markers. The reporting of these studies was often inadequate, in terms of both statistical analysis and presentation, and there was considerable heterogeneity for many important clinical/statistical factors. These problems restricted both the extraction of data and the meta-analysis of results from the primary studies, limiting feasibility of the evidence-based approach. Guidelines for reporting the results of primary prognostic marker studies in cancer, and other diseases, are given in order to facilitate both the interpretation of individual studies and the undertaking of systematic reviews, meta-analysis and, ultimately, evidence-based practice. General availability of full individual patient data is a necessary step forward and would overcome the majority of problems encountered, including poorly reported summary statistics and variability in cutoff level, outcome assessed and adjustment factors used. It would also limit the problem of reporting bias, although publication bias will remain a concern until studies are prospectively registered. Such changes in practice would help important evidence-based reviews to be conducted in order to establish the most appropriate prognostic markers for clinical use, which should ultimately improve patient care.Keywords
This publication has 70 references indexed in Scilit:
- SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometryNucleic Acids Research, 2008
- Dandruff-associated Malassezia genomes reveal convergent and divergent virulence traits shared with plant and human fungal pathogensProceedings of the National Academy of Sciences, 2007
- Comparative genome analysis across a kingdom of eukaryotic organisms: Specialization and diversification in the FungiGenome Research, 2007
- Dothideomycete–Plant Interactions Illuminated by Genome Sequencing and EST Analysis of the Wheat Pathogen Stagonospora nodorumPlant Cell, 2007
- X:Map: annotation and visualization of genome structure for Affymetrix exon array analysisNucleic Acids Research, 2007
- Independent sorting-out of thousands of duplicated gene pairs in two yeast species descended from a whole-genome duplicationProceedings of the National Academy of Sciences, 2007
- The Yeast Gene Order Browser: Combining curated homology and syntenic context reveals gene fate in polyploid speciesGenome Research, 2005
- Genome evolution in yeastsNature, 2004
- Sequencing and comparison of yeast species to identify genes and regulatory elementsNature, 2003
- The Complete Genome Sequence of Escherichia coli K-12Science, 1997