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Title: Quantification of extraprostatic extension in prostate cancer: different parameters correlated to biochemical recurrence after radical prostatectomy
Author(s): Veggel, B.A. van
Oort, I.M. van (31466811X)
Witjes, J.A. (105131768)
Kiemeney, L.A.L.M. (105132063)
Hulsbergen- van de Kaa, C.A. (298973626)
Publication year: 2011
Document type: Article / Letter to editor
Journal: Histopathology
ISSN: 0309-0167
Volume: vol. 59
Issue: iss. 4
Start page: p. 692
End page: p. 702
Annotation: van Veggel, Bianca A M H van Oort, Inge M Witjes, J Alfred Kiemeney, Lambertus A L M Hulsbergen-van de Kaa, Christina A England Histopathology. 2011 Oct;59(4):692-702. doi: 10.1111/j.1365-2559.2011.03986.x.
Abstract: AIMS: Different methods to substage extraprostatic extension (EPE) were correlated with biochemical recurrence (BCR) after radical prostatectomy (RP). Methods and results: A total of 157 consecutive RP specimens with EPE were completely embedded. Twenty-three patients with adjuvant therapy or detectable postoperative PSA levels were excluded, leaving 134 patients for BCR analysis. Data were analysed using Kaplan-Meier survival and Cox regression analyses. In univariate analysis, maximal radial distance (RD) was associated with BCR as continuous (P = 0.006) and dichotomous (P = 0.002) parameters. In multivariate analysis, independent predictors of BCR were preoperative prostate-specific antigen (PSA) (P = 0.006), Gleason score (P = 0.001), positive surgical margins (P = 0.005), maximal RD dichotomized at 0.6 mm [= one high-power field (HPF)]; hazard ratio (HR) 3.4; 95% confidence interval (CI) 1.48-7.85; P = 0.004), total RD (P = 0.009) and EPE quantification according to Epstein (P = 0.002) and to Wheeler (P = 0.004). The 5-year risk of BCR was 20% (95% CI 0.65-0.94) in patients with RD </= 0.6 mm and 47% (95% CI: 0.41-0.65) with RD > 0.6 mm. The restriction of focal EPE in no more than two slides (Epstein and Wheeler) gave no better results. CONCLUSIONS: Maximal RD dichotomized at one HPF is an objective method to subdivide EPE and a strong, independent predictor for BCR after RP. Its use is recommended for substaging pT3a in future TNM classifications.
Subject: NCEBP 1: Molecular epidemiology
NCEBP 1: Molecular epidemiology ONCOL 5: Aetiology, screening and detection
ONCOL 3: Translational research
Organization: UMCN Extern
Urology
Epidemiology, Biostatistics & HTA
Pathology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/96253

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