Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility

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Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility. / Schiffmann, Jonas; Wenzel, Philipp; Salomon, Georg; Budäus, Lars; Schlomm, Thorsten; Minner, Sarah; Wittmer, Corinna; Kraft, Stefan; Krech, Till; Steurer, Stefan; Sauter, Guido; Beyer, Burkhard; Boehm, Katharina; Tilki, Derya; Michl, Uwe; Huland, Hartwig; Graefen, Markus; Karakiewicz, Pierre I.

in: UROL ONCOL-SEMIN ORI, Jahrgang 33, Nr. 7, 07.2015, S. 329.e13-9.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Schiffmann, J, Wenzel, P, Salomon, G, Budäus, L, Schlomm, T, Minner, S, Wittmer, C, Kraft, S, Krech, T, Steurer, S, Sauter, G, Beyer, B, Boehm, K, Tilki, D, Michl, U, Huland, H, Graefen, M & Karakiewicz, PI 2015, 'Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility', UROL ONCOL-SEMIN ORI, Jg. 33, Nr. 7, S. 329.e13-9. https://doi.org/10.1016/j.urolonc.2015.04.004

APA

Schiffmann, J., Wenzel, P., Salomon, G., Budäus, L., Schlomm, T., Minner, S., Wittmer, C., Kraft, S., Krech, T., Steurer, S., Sauter, G., Beyer, B., Boehm, K., Tilki, D., Michl, U., Huland, H., Graefen, M., & Karakiewicz, P. I. (2015). Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility. UROL ONCOL-SEMIN ORI, 33(7), 329.e13-9. https://doi.org/10.1016/j.urolonc.2015.04.004

Vancouver

Bibtex

@article{8286386a0c8e4b2eae0be7fd0c07abcb,
title = "Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility",
abstract = "BACKGROUND: To date, no study has examined clinical, pathological, and surgical characteristics of D׳Amico low-risk patients according to active surveillance (AS) eligibility.MATERIAL AND METHODS: We relied on patients with low-risk prostate cancer, who were classified based on the D׳Amico classification, treated with radical prostatectomy (RP) between 2008 and 2013 at the Martini-Clinic Prostate Cancer Center. We assessed differences in clinical, pathological, and surgical characteristics in D׳Amico low-risk patients according to AS eligibility (prostate-specific antigen [PSA]≤ 10 ng/ml, Gleason score ≤ 3 + 3, ≤ 2 positive cores,≤5 0% tumor content per core, and ≤ cT1-2a). Multivariable logistic regression analyses targeted 2 end points: (1) presence of either intermediate- or high-risk characteristics (Gleason score ≥ 3+4 or ≥ pT3 or pN1) or (2) exclusive presence of high-risk characteristics (Gleason score ≥ 4+4 or ≥ pT3 or pN1) at RP.RESULTS: Of 1,331 patients low-risk prostate cancer classified based on the D׳Amico classification, 825 (62%) men were eligible for AS. AS candidates were less frequently either upgraded (55% vs. 78%, P<0.001) or upstaged (8% vs. 15%, P<0.001). Similarly, at final pathology, AS candidates less frequently harbored either intermediate- or high-risk (56% vs. 78%, P<0.001), or exclusive high-risk characteristics (9% vs. 16%, P<0.001). Tumor involvement per core (>50%) (most powerful), number of positive cores, PSA values, and age were independent predictors for either intermediate- or high-risk characteristics at RP. Tumor involvement per core and PSA values were independent predictors for exclusive high-risk characteristics at RP.CONCLUSIONS: D׳Amico low-risk patients did not have a homogeneous histology at RP. Especially, non-AS candidates were at a higher risk of either upgrading or upstaging at final pathology. Tumor involvement greater than 50% per core was the most powerful indicator of adverse pathology. Therefore, D'Amico low-risk criteria are not safe enough to identify AS candidates.",
author = "Jonas Schiffmann and Philipp Wenzel and Georg Salomon and Lars Bud{\"a}us and Thorsten Schlomm and Sarah Minner and Corinna Wittmer and Stefan Kraft and Till Krech and Stefan Steurer and Guido Sauter and Burkhard Beyer and Katharina Boehm and Derya Tilki and Uwe Michl and Hartwig Huland and Markus Graefen and Karakiewicz, {Pierre I}",
note = "Copyright {\textcopyright} 2015 Elsevier Inc. All rights reserved.",
year = "2015",
month = jul,
doi = "10.1016/j.urolonc.2015.04.004",
language = "English",
volume = "33",
pages = "329.e13--9",
journal = "UROL ONCOL-SEMIN ORI",
issn = "1078-1439",
publisher = "Elsevier Inc.",
number = "7",

}

RIS

TY - JOUR

T1 - Heterogeneity in D'Amico classification-based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility

AU - Schiffmann, Jonas

AU - Wenzel, Philipp

AU - Salomon, Georg

AU - Budäus, Lars

AU - Schlomm, Thorsten

AU - Minner, Sarah

AU - Wittmer, Corinna

AU - Kraft, Stefan

AU - Krech, Till

AU - Steurer, Stefan

AU - Sauter, Guido

AU - Beyer, Burkhard

AU - Boehm, Katharina

AU - Tilki, Derya

AU - Michl, Uwe

AU - Huland, Hartwig

AU - Graefen, Markus

AU - Karakiewicz, Pierre I

N1 - Copyright © 2015 Elsevier Inc. All rights reserved.

PY - 2015/7

Y1 - 2015/7

N2 - BACKGROUND: To date, no study has examined clinical, pathological, and surgical characteristics of D׳Amico low-risk patients according to active surveillance (AS) eligibility.MATERIAL AND METHODS: We relied on patients with low-risk prostate cancer, who were classified based on the D׳Amico classification, treated with radical prostatectomy (RP) between 2008 and 2013 at the Martini-Clinic Prostate Cancer Center. We assessed differences in clinical, pathological, and surgical characteristics in D׳Amico low-risk patients according to AS eligibility (prostate-specific antigen [PSA]≤ 10 ng/ml, Gleason score ≤ 3 + 3, ≤ 2 positive cores,≤5 0% tumor content per core, and ≤ cT1-2a). Multivariable logistic regression analyses targeted 2 end points: (1) presence of either intermediate- or high-risk characteristics (Gleason score ≥ 3+4 or ≥ pT3 or pN1) or (2) exclusive presence of high-risk characteristics (Gleason score ≥ 4+4 or ≥ pT3 or pN1) at RP.RESULTS: Of 1,331 patients low-risk prostate cancer classified based on the D׳Amico classification, 825 (62%) men were eligible for AS. AS candidates were less frequently either upgraded (55% vs. 78%, P<0.001) or upstaged (8% vs. 15%, P<0.001). Similarly, at final pathology, AS candidates less frequently harbored either intermediate- or high-risk (56% vs. 78%, P<0.001), or exclusive high-risk characteristics (9% vs. 16%, P<0.001). Tumor involvement per core (>50%) (most powerful), number of positive cores, PSA values, and age were independent predictors for either intermediate- or high-risk characteristics at RP. Tumor involvement per core and PSA values were independent predictors for exclusive high-risk characteristics at RP.CONCLUSIONS: D׳Amico low-risk patients did not have a homogeneous histology at RP. Especially, non-AS candidates were at a higher risk of either upgrading or upstaging at final pathology. Tumor involvement greater than 50% per core was the most powerful indicator of adverse pathology. Therefore, D'Amico low-risk criteria are not safe enough to identify AS candidates.

AB - BACKGROUND: To date, no study has examined clinical, pathological, and surgical characteristics of D׳Amico low-risk patients according to active surveillance (AS) eligibility.MATERIAL AND METHODS: We relied on patients with low-risk prostate cancer, who were classified based on the D׳Amico classification, treated with radical prostatectomy (RP) between 2008 and 2013 at the Martini-Clinic Prostate Cancer Center. We assessed differences in clinical, pathological, and surgical characteristics in D׳Amico low-risk patients according to AS eligibility (prostate-specific antigen [PSA]≤ 10 ng/ml, Gleason score ≤ 3 + 3, ≤ 2 positive cores,≤5 0% tumor content per core, and ≤ cT1-2a). Multivariable logistic regression analyses targeted 2 end points: (1) presence of either intermediate- or high-risk characteristics (Gleason score ≥ 3+4 or ≥ pT3 or pN1) or (2) exclusive presence of high-risk characteristics (Gleason score ≥ 4+4 or ≥ pT3 or pN1) at RP.RESULTS: Of 1,331 patients low-risk prostate cancer classified based on the D׳Amico classification, 825 (62%) men were eligible for AS. AS candidates were less frequently either upgraded (55% vs. 78%, P<0.001) or upstaged (8% vs. 15%, P<0.001). Similarly, at final pathology, AS candidates less frequently harbored either intermediate- or high-risk (56% vs. 78%, P<0.001), or exclusive high-risk characteristics (9% vs. 16%, P<0.001). Tumor involvement per core (>50%) (most powerful), number of positive cores, PSA values, and age were independent predictors for either intermediate- or high-risk characteristics at RP. Tumor involvement per core and PSA values were independent predictors for exclusive high-risk characteristics at RP.CONCLUSIONS: D׳Amico low-risk patients did not have a homogeneous histology at RP. Especially, non-AS candidates were at a higher risk of either upgrading or upstaging at final pathology. Tumor involvement greater than 50% per core was the most powerful indicator of adverse pathology. Therefore, D'Amico low-risk criteria are not safe enough to identify AS candidates.

U2 - 10.1016/j.urolonc.2015.04.004

DO - 10.1016/j.urolonc.2015.04.004

M3 - SCORING: Journal article

C2 - 25960411

VL - 33

SP - 329.e13-9

JO - UROL ONCOL-SEMIN ORI

JF - UROL ONCOL-SEMIN ORI

SN - 1078-1439

IS - 7

ER -