Clinical utility of level-of-evidence-1 disease forecast cancer biomarkers uPA and its inhibitor PAI-1

Manfred Schmitt, Karin Mengele, Rudolf Napieralski, Viktor Magdolen, Ute Reuning, Apostolos Gkazepis, Fred Sweep, Nils Brünner, John Foekens, Nadia Harbeck

Research output: Contribution to journalReview articlepeer-review

58 Scopus citations

Abstract

The prognostic and/or predictive value of the cancer biomarkers, urokinase-type plasminogen activator (uPA) and its inhibitor (plasminogen activator inhibitor [PAI]-1), determined by ELISA in tumor-tissue extracts, was demonstrated for several cancer types in numerous clinically relevant retrospective or prospective studies, including a multicenter breast cancer therapy trial (Chemo-N0). Consequently, for the first time ever for any cancer biomarker for breast cancer, uPA and PAI-1 have reached the highest level of evidence, level-of-evidence-1. At present, two other breast cancer therapy trials, NNBC-3 and Plan B, also incorporating uPA and PAI-1 as treatment-assignment tools are in effect. Furthermore, small synthetic molecules targeting uPA are currently in Phase II clinical trials in patients afflicted with advanced cancer of the ovary, breast or pancreas.

Original languageEnglish
Pages (from-to)1051-1067
Number of pages17
JournalExpert Review of Molecular Diagnostics
Volume10
Issue number8
DOIs
StatePublished - Nov 2010

Keywords

  • clinical utility
  • individualized tailored cancer care
  • personalized cancer treatment
  • predictive impact
  • prognostic relevance
  • prospective clinical trial
  • retrospective clinical study
  • targeted therapy

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