Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/121740
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dc.contributor.authorWieder, Vanessa-
dc.contributor.authorEngel, Julia-
dc.contributor.authorEichstädt, Kathleen-
dc.contributor.authorKaufhold, Sandy-
dc.contributor.authorKantelhardt, Eva Johanna-
dc.contributor.authorThomssen, Christoph-
dc.contributor.authorVetter, Martina-
dc.contributor.authorBauer, Marcus-
dc.date.accessioned2026-01-07T11:55:50Z-
dc.date.available2026-01-07T11:55:50Z-
dc.date.issued2026-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/123691-
dc.identifier.urihttp://dx.doi.org/10.25673/121740-
dc.description.abstractIntroduction An emerging challenge in early breast cancer (eBC) is improving risk assessment through the use of biomarkers. Clinical guidelines have recommended urokinase-type plasminogen activator (uPA) and its inhibitor PAI-1 for risk evaluation. This study aimed to validate the prognostic and predictive impact of uPA/PAI-1. Patients and methods From a prospective cohort of 1270 patients (PiA-study, Prognostic assessment in routine Application, NCT01592825), concentrations of uPA and PAI-1 were determined in fresh tumour tissue (n = 813) by ELISA (FEMTELLE®; LOXO Diagnostics). The uPA/PAI-1 status was defined as low if both uPA and PAI-1 levels were low and as high if one or both were elevated. Primary objectives were the distribution of the uPA/PAI-1 status and its association with clinical/histopathological parameters. Secondary objectives were the association of the uPA/PAI-1 status with recurrence-free interval (RFI), overall survival (OS), and benefit from adjuvant chemotherapy. Results A low uPA/PAI-1 status was observed in 37.6% (306 of 813) of the entire cohort and in 47.9% (181 of 378) of those classified as intermediate-risk patients (≥ 35yrs, ≤ pN1, G2, sHR positive/HER2 negative). A low uPA/PAI-1 status was associated with parameters that predict a favourable prognosis. Overall, 96.7% (95% CI 94.5–98.9) of patients with a low uPA/PAI-1-status remained recurrence-free at five years and 87.2% (95% CI 84.1–90.3) with a high uPA/PAI-1 status even after adjustment to tumour size, nodal status, grading, steroid hormone receptor (sHR) status and HER2 status (adjusted HR 2.6, 95% CI 1.29–5.23). Among intermediate-risk patients without chemotherapy (n = 197), the prognostic value was even more pronounced (HR 10.10, 95% CI 1.13–16.12). Similar results were observed for OS. Only patients with a high uPA/PAI-1 status appeared to benefit from chemotherapy (adjusted HR 0.28, 95% CI 0.07-1.12, p = 0.07). Conclusion This prospective analysis confirms the uPA/PAI-1 status as an independent prognostic factor and suggests a predictive impact considering benefit from chemotherapy.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titleProspective validation of the prognostic and predictive impact of uPA/PAI-1 in early breast cancereng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleBreast cancer research and treatment-
local.bibliographicCitation.volume215-
local.bibliographicCitation.pagestart1-
local.bibliographicCitation.pageend12-
local.bibliographicCitation.publishernameSpringer Science + Business Media B.V.-
local.bibliographicCitation.publisherplaceDordrecht [u.a.]-
local.bibliographicCitation.doi10.1007/s10549-025-07850-z-
local.openaccesstrue-
dc.identifier.ppn1947889486-
cbs.publication.displayform2026-
local.bibliographicCitation.year2026-
cbs.sru.importDate2026-01-07T11:55:22Z-
local.bibliographicCitationEnthalten in Breast cancer research and treatment - Dordrecht [u.a.] : Springer Science + Business Media B.V., 1981-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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