lunes, 4 de diciembre de 2017

Systematic review of the clinical and economic value of gene expression profiles for invasive early breast cancer available in Europe. - PubMed - NCBI

Systematic review of the clinical and economic value of gene expression profiles for invasive early breast cancer available in Europe. - PubMed - NCBI

 2017 Nov 6;62:74-90. doi: 10.1016/j.ctrv.2017.10.012. [Epub ahead of print]

Systematic review of the clinical and economic value of gene expression profiles for invasive early breast cancer available in Europe.

Abstract

Gene expression profiles with prognostic capacities have shown good performance in multiple clinical trials. However, with multiple assays available and numerous types of validation studies performed, the added value for daily clinical practice is still unclear. In Europe, the MammaPrint, OncotypeDX, PAM50/Prosigna and Endopredict assays are commercially available. In this systematic review, we aim to assess these assays on four important criteria: Assay development and methodology, clinical validation, clinical utility and economic value. We performed a literature search covering PubMed, Embase, Web of Science and Cochrane, for studies related to one or more of the four selected assays. We identified 147 papers for inclusion in this review. MammaPrint and OncotypeDX both have evidence available, including level IA clinical trial results for both assays. Both assays provide prognostic information. Predictive value has only been shown for OncotypeDX. In the clinical utility studies, a higher reduction in chemotherapy was achieved by OncotypeDX, although the number of available studies differ considerably between tests. On average, economic evaluations estimate that genomic testing results in a moderate increase in total costs, but that these costs are acceptable in relation to the expected improved patient outcome. PAM50/prosigna and EndoPredict showed comparable prognostic capacities, but with less economical and clinical utility studies. Furthermore, for these assays no level IA trial data are available yet. In summary, all assays have shown excellent prognostic capacities. The differences in the quantity and quality of evidence are discussed. Future studies shall focus on the selection of appropriate subgroups for testing and long-term outcome of validation trials, in order to determine the place of these assays in daily clinical practice.

KEYWORDS:

Breast cancer; Endopredict; Gene expression; MammaPrint; OncotypeDX; Prosigna

PMID:
 
29175678
 
DOI:
 
10.1016/j.ctrv.2017.10.012
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