Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer.

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Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer. / Steuber, Thomas; Vickers, Andrew J; Serio, Angel M; Vaisanen, Ville; Haese, Alexander; Pettersson, Kim; Eastham, James A; Scardino, Peter T; Huland, Hartwig; Lilja, Hans.

in: CLIN CHEM, Jahrgang 53, Nr. 2, 2, 2007, S. 233-240.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Steuber, T, Vickers, AJ, Serio, AM, Vaisanen, V, Haese, A, Pettersson, K, Eastham, JA, Scardino, PT, Huland, H & Lilja, H 2007, 'Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer.', CLIN CHEM, Jg. 53, Nr. 2, 2, S. 233-240. <http://www.ncbi.nlm.nih.gov/pubmed/17185368?dopt=Citation>

APA

Steuber, T., Vickers, A. J., Serio, A. M., Vaisanen, V., Haese, A., Pettersson, K., Eastham, J. A., Scardino, P. T., Huland, H., & Lilja, H. (2007). Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer. CLIN CHEM, 53(2), 233-240. [2]. http://www.ncbi.nlm.nih.gov/pubmed/17185368?dopt=Citation

Vancouver

Bibtex

@article{1135b8b97c484a729cf764cd2224baf6,
title = "Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer.",
abstract = "BACKGROUND: We evaluated the association of total and free forms of serum human kallikrein 2 (hK2) and prostate-specific antigen (PSA) with prostate cancers of unfavorable prognosis. METHODS: We retrospectively measured total PSA (tPSA), free PSA (fPSA), and total hK2 (thK2) in preoperative serum samples from 867 men [and assessed free hK2 (fhK2) measured in 577 of these men] treated with radical prostatectomy for clinically localized prostate cancer. Associations between biomarker concentrations and extracapsular extension, seminal vesicle invasion, and biochemical recurrence (BCR) were evaluated. A subset of patients with PSA <or =10 microg/L, the group most commonly seen in clinical practice in the US, was analyzed. RESULTS: thK2 was the strongest predictor of extracapsular extension and seminal vesicle invasion (areas under the ROC curve [AUC], 0.662 and 0.719, respectively), followed by tPSA (AUC, 0.654 and 0.663). All biomarkers were significant predictors of BCR. hK2 forms, but not PSA forms, remained highly significant for predicting BCR in the low-PSA group. Combining tPSA, fPSA, and thK2 in a multivariable model improved prediction compared with any biomarker used individually (AUC, 0.711, 0.755, and 0.752 for this combination predicting extracapsular extension, seminal vesicle invasion, and BCR, respectively; P",
author = "Thomas Steuber and Vickers, {Andrew J} and Serio, {Angel M} and Ville Vaisanen and Alexander Haese and Kim Pettersson and Eastham, {James A} and Scardino, {Peter T} and Hartwig Huland and Hans Lilja",
year = "2007",
language = "Deutsch",
volume = "53",
pages = "233--240",
journal = "CLIN CHEM",
issn = "0009-9147",
publisher = "American Association for Clinical Chemistry Inc.",
number = "2",

}

RIS

TY - JOUR

T1 - Comparison of free and total forms of serum human kallikrein 2 and prostate-specific antigen for prediction of locally advanced and recurrent prostate cancer.

AU - Steuber, Thomas

AU - Vickers, Andrew J

AU - Serio, Angel M

AU - Vaisanen, Ville

AU - Haese, Alexander

AU - Pettersson, Kim

AU - Eastham, James A

AU - Scardino, Peter T

AU - Huland, Hartwig

AU - Lilja, Hans

PY - 2007

Y1 - 2007

N2 - BACKGROUND: We evaluated the association of total and free forms of serum human kallikrein 2 (hK2) and prostate-specific antigen (PSA) with prostate cancers of unfavorable prognosis. METHODS: We retrospectively measured total PSA (tPSA), free PSA (fPSA), and total hK2 (thK2) in preoperative serum samples from 867 men [and assessed free hK2 (fhK2) measured in 577 of these men] treated with radical prostatectomy for clinically localized prostate cancer. Associations between biomarker concentrations and extracapsular extension, seminal vesicle invasion, and biochemical recurrence (BCR) were evaluated. A subset of patients with PSA <or =10 microg/L, the group most commonly seen in clinical practice in the US, was analyzed. RESULTS: thK2 was the strongest predictor of extracapsular extension and seminal vesicle invasion (areas under the ROC curve [AUC], 0.662 and 0.719, respectively), followed by tPSA (AUC, 0.654 and 0.663). All biomarkers were significant predictors of BCR. hK2 forms, but not PSA forms, remained highly significant for predicting BCR in the low-PSA group. Combining tPSA, fPSA, and thK2 in a multivariable model improved prediction compared with any biomarker used individually (AUC, 0.711, 0.755, and 0.752 for this combination predicting extracapsular extension, seminal vesicle invasion, and BCR, respectively; P

AB - BACKGROUND: We evaluated the association of total and free forms of serum human kallikrein 2 (hK2) and prostate-specific antigen (PSA) with prostate cancers of unfavorable prognosis. METHODS: We retrospectively measured total PSA (tPSA), free PSA (fPSA), and total hK2 (thK2) in preoperative serum samples from 867 men [and assessed free hK2 (fhK2) measured in 577 of these men] treated with radical prostatectomy for clinically localized prostate cancer. Associations between biomarker concentrations and extracapsular extension, seminal vesicle invasion, and biochemical recurrence (BCR) were evaluated. A subset of patients with PSA <or =10 microg/L, the group most commonly seen in clinical practice in the US, was analyzed. RESULTS: thK2 was the strongest predictor of extracapsular extension and seminal vesicle invasion (areas under the ROC curve [AUC], 0.662 and 0.719, respectively), followed by tPSA (AUC, 0.654 and 0.663). All biomarkers were significant predictors of BCR. hK2 forms, but not PSA forms, remained highly significant for predicting BCR in the low-PSA group. Combining tPSA, fPSA, and thK2 in a multivariable model improved prediction compared with any biomarker used individually (AUC, 0.711, 0.755, and 0.752 for this combination predicting extracapsular extension, seminal vesicle invasion, and BCR, respectively; P

M3 - SCORING: Zeitschriftenaufsatz

VL - 53

SP - 233

EP - 240

JO - CLIN CHEM

JF - CLIN CHEM

SN - 0009-9147

IS - 2

M1 - 2

ER -