Relationship between cathepsin-D content and disease-free survival in node-negative breast cancer patients: a meta-analysis
- PMID: 9303368
- PMCID: PMC2228021
- DOI: 10.1038/bjc.1997.442
Relationship between cathepsin-D content and disease-free survival in node-negative breast cancer patients: a meta-analysis
Abstract
Several reports have evaluated the correlation between cathepsin-D and overall survival or disease-free survival in node-negative breast cancer patients. Because conflicting data have so far been reported, a meta-analysis was conducted to clarify this problem. Eleven studies were included in our meta-analysis (total of 2690 patients). A specific meta-analytical methodology for censored data was used, and disease-free survival was the primary end point. Patients with low cathepsin-D levels had a significantly better disease-free survival than patients with high cathepsin-D values (meta-analytical odds ratio from 0.59 to 0.60 over the interval from 1 to 7 years). A secondary meta-analysis conducted exclusively on the data from eight studies based on cytosol assay gave substantially similar results. One limitation of our study is that the cut-off values to define high and low cathepsin-D concentrations were not identical in the various studies included in our meta-analysis (range from 20 to 78 pmol mg(-1) protein), thus introducing a possible bias in the statistical analysis of the data. However, a simulation based on the well-accepted method of the so-called publication bias showed that more than 100 null studies would be required to lead our results to a statistical level of non-significance. Considering the results of our meta-analysis, we conclude that the data presently available confirm a statistically significant association between high cathepsin-D values and poor disease-free survival in node-negative breast cancer patients.
Comment in
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Suboptimal analysis using 'optimal' cutpoints.Br J Cancer. 1998 Aug;78(4):556-7. doi: 10.1038/bjc.1998.537. Br J Cancer. 1998. PMID: 9716046 Free PMC article. No abstract available.
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