2012
DOI: 10.1007/s00432-012-1351-7
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The role of treatment modality on the utility of predictive tissue biomarkers in clinical prostate cancer: a systematic review

Abstract: Despite years of research, very few tissue biomarkers retain predictive value in independent validation across therapy context. Currently, none have conclusive ability to help treatment selection. Future biomarker research should consider the therapy context and use uniform methodology and evaluation criteria.

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Cited by 20 publications
(21 citation statements)
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“…Candidate biomarkers were identified from a recent systematic review and had shown prognostic value in surgical cohorts but had not been tested in other therapies: E Cadherin, EGFR, EZH2, PTEN and MSMB [3]. These markers are also exemplars of biological events that are critical to prostate cancer progression (metastasis, growth factor signalling, transcription factor, cell survival and inhibitor of prostate cancer growth).…”
Section: Methodsmentioning
confidence: 99%
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“…Candidate biomarkers were identified from a recent systematic review and had shown prognostic value in surgical cohorts but had not been tested in other therapies: E Cadherin, EGFR, EZH2, PTEN and MSMB [3]. These markers are also exemplars of biological events that are critical to prostate cancer progression (metastasis, growth factor signalling, transcription factor, cell survival and inhibitor of prostate cancer growth).…”
Section: Methodsmentioning
confidence: 99%
“…The prostate marker PSMA which has shown promise as a prognostic marker following surgery but has not been tested in other treatment cohorts [8, 9]. We also included the androgen receptor (AR) which has not been tested in EBRT therapy as well as the generic marker prostate cancer antigen 3 (PCA3) [3, 10, 11]. All three were also selected as they are very well described genes expressed in prostate tissue and in prostate cancer.…”
Section: Methodsmentioning
confidence: 99%
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