Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk

Standard

Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk. / Schiffmann, Jonas; Connan, Judith; Salomon, Georg; Boehm, Katharina; Beyer, Burkhard; Schlomm, Thorsten; Tennstedt, Pierre; Sauter, Guido; Karakiewicz, Pierre I; Graefen, Markus; Huland, Hartwig.

In: PROSTATE, Vol. 75, No. 1, 01.01.2015, p. 45-9.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Schiffmann, J, Connan, J, Salomon, G, Boehm, K, Beyer, B, Schlomm, T, Tennstedt, P, Sauter, G, Karakiewicz, PI, Graefen, M & Huland, H 2015, 'Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk', PROSTATE, vol. 75, no. 1, pp. 45-9. https://doi.org/10.1002/pros.22889

APA

Schiffmann, J., Connan, J., Salomon, G., Boehm, K., Beyer, B., Schlomm, T., Tennstedt, P., Sauter, G., Karakiewicz, P. I., Graefen, M., & Huland, H. (2015). Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk. PROSTATE, 75(1), 45-9. https://doi.org/10.1002/pros.22889

Vancouver

Schiffmann J, Connan J, Salomon G, Boehm K, Beyer B, Schlomm T et al. Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk. PROSTATE. 2015 Jan 1;75(1):45-9. https://doi.org/10.1002/pros.22889

Bibtex

@article{f7493663bd7a4690a4e641431bec8b81,
title = "Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk",
abstract = "BACKGROUND: An increased tumor volume threshold (<2.5 ml) is suggested to define insignificant prostate cancer (iPCa). We hypothesize that an increasing tumor volume within iPCa patients increases the risk of biochemical recurrence (BCR) after radical prostatectomy (RP).METHODS: We relied on RP patients treated between 1992 and 2008. Multivariable Cox regression analyses predicting BCR within patients harboring favorable pathological characteristics (≤pT2, pN0/Nx, Gleason 3 + 3). Kaplan-Meier analysis was performed for BCR-free survival within iPCa patients (≤pT2, pN0/Nx, Gleason 3 + 3, tumor volume: <0.5 vs. 0.5-2.49 ml).RESULTS: From 1,829 patients, 141 (7.7%) and 310 (16.9%) harbored iPCa (tumor volume: <0.5 vs. 0.5-2.49 ml), respectively. Of those, 21 (14.9%) versus 31 (10.0%) had PSA >10 ng/ml. Tumor volume achieved independent predictor status for BCR. Specifically, iPCa patients with increasing tumor volume (0.5-2.49 ml) were at higher risk of BCR after RP than those with tumor volume <0.5 ml (HR: 8.8, 95% CI: 1.2-65.9, P = 0.04). Kaplan-Meier analysis recorded superior BCR-free survival in iPCa patients with lower tumor volume (<0.5 ml) (log-rank P = 0.009). The 10-year cancer-specific death rate was 0 versus 0.5%.CONCLUSIONS: Contemporary iPCa definition incorporates intermediate and high-risk patients (PSA: 10-20 and >20 ng/ml). Despite most favorable pathological characteristics, iPCa patients are not devoid of BCR after RP. Moreover, iPCa patients were at higher risk of BCR, when increasing tumor volume up to 2.49 ml was at play. Taken together the contemporary concept of iPCa is suboptimal. Especially, an increased tumor volume threshold for defining iPCa cannot be recommended according to our data. Clinicians might take these considerations into account during decision-making process.",
keywords = "Aged, Disease-Free Survival, Humans, Male, Middle Aged, Neoplasm Recurrence, Local, Prognosis, Prostate, Prostatectomy, Prostatic Neoplasms, Regression Analysis, Risk, Survival Analysis, Tumor Burden",
author = "Jonas Schiffmann and Judith Connan and Georg Salomon and Katharina Boehm and Burkhard Beyer and Thorsten Schlomm and Pierre Tennstedt and Guido Sauter and Karakiewicz, {Pierre I} and Markus Graefen and Hartwig Huland",
note = "{\textcopyright} 2014 Wiley Periodicals, Inc.",
year = "2015",
month = jan,
day = "1",
doi = "10.1002/pros.22889",
language = "English",
volume = "75",
pages = "45--9",
journal = "PROSTATE",
issn = "0270-4137",
publisher = "Wiley-Liss Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Tumor volume in insignificant prostate cancer: increasing threshold gains increasing risk

AU - Schiffmann, Jonas

AU - Connan, Judith

AU - Salomon, Georg

AU - Boehm, Katharina

AU - Beyer, Burkhard

AU - Schlomm, Thorsten

AU - Tennstedt, Pierre

AU - Sauter, Guido

AU - Karakiewicz, Pierre I

AU - Graefen, Markus

AU - Huland, Hartwig

N1 - © 2014 Wiley Periodicals, Inc.

PY - 2015/1/1

Y1 - 2015/1/1

N2 - BACKGROUND: An increased tumor volume threshold (<2.5 ml) is suggested to define insignificant prostate cancer (iPCa). We hypothesize that an increasing tumor volume within iPCa patients increases the risk of biochemical recurrence (BCR) after radical prostatectomy (RP).METHODS: We relied on RP patients treated between 1992 and 2008. Multivariable Cox regression analyses predicting BCR within patients harboring favorable pathological characteristics (≤pT2, pN0/Nx, Gleason 3 + 3). Kaplan-Meier analysis was performed for BCR-free survival within iPCa patients (≤pT2, pN0/Nx, Gleason 3 + 3, tumor volume: <0.5 vs. 0.5-2.49 ml).RESULTS: From 1,829 patients, 141 (7.7%) and 310 (16.9%) harbored iPCa (tumor volume: <0.5 vs. 0.5-2.49 ml), respectively. Of those, 21 (14.9%) versus 31 (10.0%) had PSA >10 ng/ml. Tumor volume achieved independent predictor status for BCR. Specifically, iPCa patients with increasing tumor volume (0.5-2.49 ml) were at higher risk of BCR after RP than those with tumor volume <0.5 ml (HR: 8.8, 95% CI: 1.2-65.9, P = 0.04). Kaplan-Meier analysis recorded superior BCR-free survival in iPCa patients with lower tumor volume (<0.5 ml) (log-rank P = 0.009). The 10-year cancer-specific death rate was 0 versus 0.5%.CONCLUSIONS: Contemporary iPCa definition incorporates intermediate and high-risk patients (PSA: 10-20 and >20 ng/ml). Despite most favorable pathological characteristics, iPCa patients are not devoid of BCR after RP. Moreover, iPCa patients were at higher risk of BCR, when increasing tumor volume up to 2.49 ml was at play. Taken together the contemporary concept of iPCa is suboptimal. Especially, an increased tumor volume threshold for defining iPCa cannot be recommended according to our data. Clinicians might take these considerations into account during decision-making process.

AB - BACKGROUND: An increased tumor volume threshold (<2.5 ml) is suggested to define insignificant prostate cancer (iPCa). We hypothesize that an increasing tumor volume within iPCa patients increases the risk of biochemical recurrence (BCR) after radical prostatectomy (RP).METHODS: We relied on RP patients treated between 1992 and 2008. Multivariable Cox regression analyses predicting BCR within patients harboring favorable pathological characteristics (≤pT2, pN0/Nx, Gleason 3 + 3). Kaplan-Meier analysis was performed for BCR-free survival within iPCa patients (≤pT2, pN0/Nx, Gleason 3 + 3, tumor volume: <0.5 vs. 0.5-2.49 ml).RESULTS: From 1,829 patients, 141 (7.7%) and 310 (16.9%) harbored iPCa (tumor volume: <0.5 vs. 0.5-2.49 ml), respectively. Of those, 21 (14.9%) versus 31 (10.0%) had PSA >10 ng/ml. Tumor volume achieved independent predictor status for BCR. Specifically, iPCa patients with increasing tumor volume (0.5-2.49 ml) were at higher risk of BCR after RP than those with tumor volume <0.5 ml (HR: 8.8, 95% CI: 1.2-65.9, P = 0.04). Kaplan-Meier analysis recorded superior BCR-free survival in iPCa patients with lower tumor volume (<0.5 ml) (log-rank P = 0.009). The 10-year cancer-specific death rate was 0 versus 0.5%.CONCLUSIONS: Contemporary iPCa definition incorporates intermediate and high-risk patients (PSA: 10-20 and >20 ng/ml). Despite most favorable pathological characteristics, iPCa patients are not devoid of BCR after RP. Moreover, iPCa patients were at higher risk of BCR, when increasing tumor volume up to 2.49 ml was at play. Taken together the contemporary concept of iPCa is suboptimal. Especially, an increased tumor volume threshold for defining iPCa cannot be recommended according to our data. Clinicians might take these considerations into account during decision-making process.

KW - Aged

KW - Disease-Free Survival

KW - Humans

KW - Male

KW - Middle Aged

KW - Neoplasm Recurrence, Local

KW - Prognosis

KW - Prostate

KW - Prostatectomy

KW - Prostatic Neoplasms

KW - Regression Analysis

KW - Risk

KW - Survival Analysis

KW - Tumor Burden

U2 - 10.1002/pros.22889

DO - 10.1002/pros.22889

M3 - SCORING: Journal article

C2 - 25284155

VL - 75

SP - 45

EP - 49

JO - PROSTATE

JF - PROSTATE

SN - 0270-4137

IS - 1

ER -