Evidence map›Paper›PMID 25129371›Full record

ArticleVirchows Archiv : an international journal of pathology2014

Maximum tumor diameter adjusted to the risk profile predicts biochemical recurrence after radical prostatectomy.

Georg Müller, Malte Rieken, Gernot Bonkat, Joel Roman Gsponer, Tatjana Vlajnic, Christian Wetterauer, Thomas C Gasser, Stephen F Wyler, Alexander Bachmann, Lukas Bubendorf

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Article in Virchows Archiv : an international journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Georg MüllerDepartment of Urology, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland, georg.mueller@usb.ch.
Malte Rieken
Gernot Bonkat
Joel Roman Gsponer
Tatjana Vlajnic
Christian Wetterauer
Thomas C Gasser
Stephen F Wyler
Alexander Bachmann
Lukas Bubendorf

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, no consensus exists on the best method for tumor quantification in prostate cancer (PCA), and its prognostic value remains controversial. We evaluated how a newly defined maximum tumor diameter (MTD) might contribute to the prediction of biochemical recurrence (BCR) in a consecutive series of PCA patients treated with radical prostatectomy (RP). Patients with PCA who underwent RP without neoadjuvant therapy at a single center were included for analysis. MTD was defined as the largest diameter of all identified tumors in all three dimensions (i.e., length, width, or depth) of the prostate ("Basel technique"). Cox regression models addressed the association of MTD with BCR in three risk groups (low risk-prostate-specific antigen (PSA) < 10 ng/ml, pT2, and Gleason score (GS) ≤ 6; intermediate risk-PSA ≥ 10 and <20 ng/ml and/or pT2 and GS = 7; high risk-PSA > 20 ng/ml or pT3 or GS ≥ 8) and whole cohort. Within a median follow-up of 44 months (interquartile range (IQR) 23-66), 48 patients (9.4 %) in the intermediate-risk and high-risk groups experienced BCR. In multivariate Cox regression analysis, PSA, pathological stage (pT stage), GS, positive surgical margins (PSMs), and MTD > 19.5 mm were independent predictors for BCR (p < 0.05). In subgroup analysis, MTD as a nominal variable (<24.5 and >24.5 mm) was the only independent predictor of BCR in the intermediate-risk group (hazard ratio (HR) 9.933, 95 % confidence interval (CI) 2.070-47.665; p < 0.05). MTD is an independent risk factor of BCR in PC patients after RP. The combination of the MTD with other well-known prognostic factors after RP may improve decision-making concerning follow-up intensity or adjuvant treatment.

Indexed as

AgedHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingPredictive Value of TestsProportional Hazards ModelsProstatectomyProstatic NeoplasmsRisk FactorsROC Curve

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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.