External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy.

Standard

External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy. / Shariat, Shahrokh F; Walz, Jochen; Roehrborn, Claus G; Zlotta, Alexandre R; Perrotte, Paul; Suardi, Nazareno; Saad, Fred; Karakiewicz, Pierre I.

In: J CLIN ONCOL, Vol. 26, No. 9, 9, 2008, p. 1526-1531.

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

Harvard

Shariat, SF, Walz, J, Roehrborn, CG, Zlotta, AR, Perrotte, P, Suardi, N, Saad, F & Karakiewicz, PI 2008, 'External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy.', J CLIN ONCOL, vol. 26, no. 9, 9, pp. 1526-1531. <http://www.ncbi.nlm.nih.gov/pubmed/18349404?dopt=Citation>

APA

Shariat, S. F., Walz, J., Roehrborn, C. G., Zlotta, A. R., Perrotte, P., Suardi, N., Saad, F., & Karakiewicz, P. I. (2008). External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy. J CLIN ONCOL, 26(9), 1526-1531. [9]. http://www.ncbi.nlm.nih.gov/pubmed/18349404?dopt=Citation

Vancouver

Shariat SF, Walz J, Roehrborn CG, Zlotta AR, Perrotte P, Suardi N et al. External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy. J CLIN ONCOL. 2008;26(9):1526-1531. 9.

Bibtex

@article{398772d115644713aee622a760f53cee,
title = "External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy.",
abstract = "PURPOSE: Biomarker signatures currently are used in several malignancies to guide clinical decision making. Recently, preoperative plasma levels of transforming growth factor-beta1 (TGF-beta1) and interleukin-6 soluble receptor (IL6-SR) have improved the accuracy of a clinical nomogram that predicted biochemical recurrence after radical prostatectomy. However, this model was never externally validated. We tested the accuracy of this nomogram in an independent, external cohort. PATIENTS AND METHODS: Preoperative plasma levels of TGF-beta1 and IL6-SR were measured in 423 consecutive men who underwent radical prostatectomy and bilateral lymphadenectomy and were used, along with preoperative prostate-specific antigen levels, biopsy Gleason sum, and clinical stage to determine nomogram-derived probabilities of biochemical recurrence-free survival at 5 years after radical prostatectomy. The accuracy of predictions was quantified with the area under the curve (AUC) and calibration plots that graphically displayed the nomogram's performance characteristics. The statistical significance of the difference between the biomarker nomogram and a model designed on the basis of clinical variables alone was tested by using the Mantel-Haenszel statistic. RESULTS: Biochemical recurrence-free survival at 5 years was 77.0% (95% CI, 72.0% to 82.0%). The biomarker-based nomogram was 87.9% accurate versus 71.1% for the nomogram designed on the basis of clinical variables alone (16.8% difference; P <.001). The performance characteristics of the biomarker-based nomogram were superior to those of the clinical nomogram. CONCLUSION: We confirm that plasma levels of TGF-beta1 and IL6-SR considerably enhance the accuracy of the standard preoperative nomogram for the prediction of biochemical recurrence after radical prostatectomy. This model further refines our ability to identify patients at a high risk of biochemical recurrence after radical prostatectomy.",
author = "Shariat, {Shahrokh F} and Jochen Walz and Roehrborn, {Claus G} and Zlotta, {Alexandre R} and Paul Perrotte and Nazareno Suardi and Fred Saad and Karakiewicz, {Pierre I}",
year = "2008",
language = "Deutsch",
volume = "26",
pages = "1526--1531",
journal = "J CLIN ONCOL",
issn = "0732-183X",
publisher = "American Society of Clinical Oncology",
number = "9",

}

RIS

TY - JOUR

T1 - External validation of a biomarker-based preoperative nomogram predicts biochemical recurrence after radical prostatectomy.

AU - Shariat, Shahrokh F

AU - Walz, Jochen

AU - Roehrborn, Claus G

AU - Zlotta, Alexandre R

AU - Perrotte, Paul

AU - Suardi, Nazareno

AU - Saad, Fred

AU - Karakiewicz, Pierre I

PY - 2008

Y1 - 2008

N2 - PURPOSE: Biomarker signatures currently are used in several malignancies to guide clinical decision making. Recently, preoperative plasma levels of transforming growth factor-beta1 (TGF-beta1) and interleukin-6 soluble receptor (IL6-SR) have improved the accuracy of a clinical nomogram that predicted biochemical recurrence after radical prostatectomy. However, this model was never externally validated. We tested the accuracy of this nomogram in an independent, external cohort. PATIENTS AND METHODS: Preoperative plasma levels of TGF-beta1 and IL6-SR were measured in 423 consecutive men who underwent radical prostatectomy and bilateral lymphadenectomy and were used, along with preoperative prostate-specific antigen levels, biopsy Gleason sum, and clinical stage to determine nomogram-derived probabilities of biochemical recurrence-free survival at 5 years after radical prostatectomy. The accuracy of predictions was quantified with the area under the curve (AUC) and calibration plots that graphically displayed the nomogram's performance characteristics. The statistical significance of the difference between the biomarker nomogram and a model designed on the basis of clinical variables alone was tested by using the Mantel-Haenszel statistic. RESULTS: Biochemical recurrence-free survival at 5 years was 77.0% (95% CI, 72.0% to 82.0%). The biomarker-based nomogram was 87.9% accurate versus 71.1% for the nomogram designed on the basis of clinical variables alone (16.8% difference; P <.001). The performance characteristics of the biomarker-based nomogram were superior to those of the clinical nomogram. CONCLUSION: We confirm that plasma levels of TGF-beta1 and IL6-SR considerably enhance the accuracy of the standard preoperative nomogram for the prediction of biochemical recurrence after radical prostatectomy. This model further refines our ability to identify patients at a high risk of biochemical recurrence after radical prostatectomy.

AB - PURPOSE: Biomarker signatures currently are used in several malignancies to guide clinical decision making. Recently, preoperative plasma levels of transforming growth factor-beta1 (TGF-beta1) and interleukin-6 soluble receptor (IL6-SR) have improved the accuracy of a clinical nomogram that predicted biochemical recurrence after radical prostatectomy. However, this model was never externally validated. We tested the accuracy of this nomogram in an independent, external cohort. PATIENTS AND METHODS: Preoperative plasma levels of TGF-beta1 and IL6-SR were measured in 423 consecutive men who underwent radical prostatectomy and bilateral lymphadenectomy and were used, along with preoperative prostate-specific antigen levels, biopsy Gleason sum, and clinical stage to determine nomogram-derived probabilities of biochemical recurrence-free survival at 5 years after radical prostatectomy. The accuracy of predictions was quantified with the area under the curve (AUC) and calibration plots that graphically displayed the nomogram's performance characteristics. The statistical significance of the difference between the biomarker nomogram and a model designed on the basis of clinical variables alone was tested by using the Mantel-Haenszel statistic. RESULTS: Biochemical recurrence-free survival at 5 years was 77.0% (95% CI, 72.0% to 82.0%). The biomarker-based nomogram was 87.9% accurate versus 71.1% for the nomogram designed on the basis of clinical variables alone (16.8% difference; P <.001). The performance characteristics of the biomarker-based nomogram were superior to those of the clinical nomogram. CONCLUSION: We confirm that plasma levels of TGF-beta1 and IL6-SR considerably enhance the accuracy of the standard preoperative nomogram for the prediction of biochemical recurrence after radical prostatectomy. This model further refines our ability to identify patients at a high risk of biochemical recurrence after radical prostatectomy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 26

SP - 1526

EP - 1531

JO - J CLIN ONCOL

JF - J CLIN ONCOL

SN - 0732-183X

IS - 9

M1 - 9

ER -