Evidence map›Paper›PMID 35689881›Full record

Trial reportBreast (Edinburgh, Scotland)2022

Independent validation of stromal uPA in ABCSG-08: Level 1b evidence for the prognostic value of uPA immunohistochemistry.

C F Singer, S W Jahn, M Rudas, Z Bago-Horvath, F Fitzal, L Abete, F Moinfar, M Gnant, M Filipits, Austrian Breast and Colorectal Cancer Study Group (ABCSG)

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Breast (Edinburgh, Scotland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

C F SingerDept of OB/GYN, Austria; Comprehensive Cancer Center, Austria. Electronic address: christian.singer@meduniwien.ac.at.
S W JahnDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
M RudasDept of Pathology, Austria.
Z Bago-HorvathDept of Pathology, Austria.
F FitzalDept of Surgery, Austria; Comprehensive Cancer Center, Austria.
L AbeteDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
F MoinfarInstitute for Clinical Pathology and Molecular Pathology, Sisters of Mercy Hospital, Linz, Austria.
M GnantComprehensive Cancer Center, Austria.
M FilipitsDept of Internal Medicine I, Austria; Comprehensive Cancer Center, Austria; Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Austrian Breast and Colorectal Cancer Study Group (ABCSG)
Comprehensive Cancer Center Vienna · ATMedical University of Graz · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo validate the prognostic role of urokinase-type plasminogen-activator (uPA) and plasminogen activator inhibitor type-1 (PAI-1) protein expression in FFPE archived tumor samples when assessed by immunohistochemistry. PATIENTS AND

methodsFresh-frozen, paraffin-embedded (FFPE) samples from 303 postmenopausal women with hormone receptor-positive, early breast cancer were investigated. The patients had received 5 years of endocrine therapy in the prospectively randomized ABCSG-8 trial. Immunohistochemistry for stromal uPA and PAI-1 protein expression was correlated with distant recurrence-free survival (DRFS) and overall survival (OS).

resultsWe detected stromal uPA in 132 of 297 tumors (44.4%) and stromal PAI-1 expression in 74 out of 299 samples (24.7%). Co-expression of uPA and PAI-1 was present in 48 of 294 (16.3%) cases. Neither uPA nor PAI-1 expression was associated with tumor size, age, nodal status, grading, or quantitative receptor status. Patients whose tumor stroma expressed uPA protein had a significantly shorter DRFS (adjusted HR for relapse: 2.78; 95% CI 1.31-5.93; p = 0.008 Cox regression analysis) than women without uPA expression. No such association was seen for PAI-1 and the uPA/PAI1 ratio. After a median follow-up of 5.6 years, women with uPA-positive tumors demonstrated significantly shorter DRFS (93.3% vs. 84.8%; p < 0.013 log-rank test), and tended to have a worse OS (83.0% vs. 77.3%; p = 0.106) compared to women with uPA negative tumors.

conclusionThis independent validation in archived tumor samples from a large prospective randomized trial confirms the clinical utility of stromal uPA evaluation by immunohistochemistry. This provides level 1b evidence for the prognostic role of stromal uPA in women with endocrine-responsive early breast cancer.

Indexed as

Breast NeoplasmsUrokinase-Type Plasminogen ActivatorFemaleHumansImmunohistochemistryNeoplasm Recurrence, LocalPlasminogen Activator Inhibitor 1PrognosisProspective StudiesPlasminogen Activator Inhibitor 1Urokinase-Type Plasminogen ActivatorABCSG 8Adjuvant endocrine therapyBreast cancerPlasminogen activator Inhibitor-1 (PAI-1)Urokinase plasminogen activator (uPA)

Identifiers

PMID35689881
PMCPMC9190055
OpenAlexW4280589347

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.