Literature DB >> 25344896

Multi-institutional validation of the prognostic value of Ki-67 labeling index in patients treated with radical prostatectomy.

Romain Mathieu1, Shahrokh F Shariat, Christian Seitz, Pierre I Karakiewicz, Harun Fajkovic, Maxine Sun, Yair Lotan, Douglas S Scherr, Ashutosh Tewari, Francesco Montorsi, Alberto Briganti, Morgan Rouprêt, Ilaria Lucca, Vitaly Margulis, Michael Rink, Luis A Kluth, Malte Rieken, Alexander Bachman, Evanguelos Xylinas, Brian D Robinson, Karim Bensalah, Markus Margreiter.   

Abstract

OBJECTIVE: Several smaller single-center studies have reported a prognostic role for Ki-67 labeling index in prostate cancer. Our aim was to test whether Ki-67 is an independent prognostic marker of biochemical recurrence (BCR) in a large international cohort of patients treated with radical prostatectomy (RP).
METHODS: Ki-67 immunohistochemical staining on prostatectomy specimens from 3,123 patients who underwent RP for prostate cancer was retrospectively performed. Univariable and multivariable Cox regression models were used to assess the association of Ki-67 status with BCR.
RESULTS: Ki-67 positive status was observed in 762 (24.4 %) patients and was associated with lymph node involvement (LNI) (p = 0.039). Six hundred and twenty-one (19.9 %) patients experienced BCR. The estimated 3-year biochemical-free survivals were 85 % for patients with negative Ki-67 status and 82.1 % for patients with positive Ki-67 status (log-rank test, p = 0.014). In multivariable analysis that adjusted for the effects of age, preoperative PSA, RP Gleason sum, seminal vesicle invasion, extracapsular extension, positive surgical margins, lymphovascular invasion, and LNI, Ki-67 was significantly associated with BCR (HR = 1.19; p = 0.019). Subgroup analysis revealed that Ki-67 is associated with BCR in patients without LNI (p = 0.004), those with RP Gleason sum 7 (p = 0.015), and those with negative surgical margins (p = 0.047).
CONCLUSION: We confirmed Ki-67 as an independent predictor of BCR after RP. Ki-67 could be particularly informative in patients with favorable pathologic characteristics to help in the clinical decision-making regarding adjuvant therapy and optimized follow-up scheduling.

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Year:  2014        PMID: 25344896     DOI: 10.1007/s00345-014-1421-3

Source DB:  PubMed          Journal:  World J Urol        ISSN: 0724-4983            Impact factor:   4.226


  30 in total

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2.  Fresh tissue harvest for research from prostatectomy specimens.

Authors:  T M Wheeler; R M Lebovitz
Journal:  Prostate       Date:  1994-11       Impact factor: 4.104

3.  Perineural invasion and MIB-1 positivity in addition to Gleason score are significant preoperative predictors of progression after radical retropubic prostatectomy for prostate cancer.

Authors:  Thomas J Sebo; John C Cheville; Darren L Riehle; Christine M Lohse; V Shane Pankratz; Robert P Myers; Michael L Blute; Horst Zincke
Journal:  Am J Surg Pathol       Date:  2002-04       Impact factor: 6.394

4.  Cell proliferation in prostate cancer patients with lymph node metastasis: a marker for progression.

Authors:  L Cheng; T M Pisansky; T J Sebo; B C Leibovich; D M Ramnani; A L Weaver; B G Scherer; M L Blute; H Zincke; D G Bostwick
Journal:  Clin Cancer Res       Date:  1999-10       Impact factor: 12.531

5.  p27(kip1) and Ki-67 (MIB1) immunohistochemical expression in radical prostatectomy specimens of patients with clinically localized prostate cancer.

Authors:  Kyriakos Revelos; Constantina Petraki; Alkiviadis Gregorakis; Andreas Scorilas; Panagiotis Papanastasiou; Roxane Tenta; Michael Koutsilieris
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6.  Androgen receptor, Ki67, and p53 expression in radical prostatectomy specimens predict treatment failure in Japanese population.

Authors:  Takahiro Inoue; Takehiko Segawa; Taizou Shiraishi; Toru Yoshida; Yoshinobu Toda; Tomomi Yamada; Naoko Kinukawa; Hidefumi Kinoshita; Toshiyuki Kamoto; Osamu Ogawa
Journal:  Urology       Date:  2005-08       Impact factor: 2.649

7.  Monoclonal antibody Ki-67 defined growth fraction in benign prostatic hyperplasia and prostatic cancer.

Authors:  M P Gallee; E Visser-de Jong; F J ten Kate; F H Schroeder; T H Van der Kwast
Journal:  J Urol       Date:  1989-11       Impact factor: 7.450

8.  Beyond prostate-specific antigen: new serologic biomarkers for improved diagnosis and management of prostate cancer.

Authors:  Shahrokh F Shariat; Eduardo I Canto; Michael W Kattan; Kevin M Slawin
Journal:  Rev Urol       Date:  2004

9.  Biochemical outcome after radical prostatectomy or external beam radiation therapy for patients with clinically localized prostate carcinoma in the prostate specific antigen era.

Authors:  Anthony V D'Amico; Richard Whittington; S Bruce Malkowicz; Kerri Cote; Marian Loffredo; Delray Schultz; Ming-Hui Chen; John E Tomaszewski; Andrew A Renshaw; Alan Wein; Jerome P Richie
Journal:  Cancer       Date:  2002-07-15       Impact factor: 6.860

Review 10.  Challenges of cancer biomarker profiling.

Authors:  Karim Bensalah; Francesco Montorsi; Shahrokh F Shariat
Journal:  Eur Urol       Date:  2007-10-01       Impact factor: 20.096

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  5 in total

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Journal:  Biomark Med       Date:  2018-06-15       Impact factor: 2.851

2.  Comparison of cell cycle progression score with two immunohistochemical markers (PTEN and Ki-67) for predicting outcome in prostate cancer after radical prostatectomy.

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Journal:  World J Urol       Date:  2018-04-20       Impact factor: 4.226

3.  Comparison of digital image analysis and visual scoring of KI-67 in prostate cancer prognosis after prostatectomy.

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Journal:  Diagn Pathol       Date:  2015-06-13       Impact factor: 2.644

4.  Ki-67, topoisomerase IIα and miR-221 have a limited prostate cancer risk stratification ability on a medium-term follow-up: results of a high-risk radical prostatectomy cohort.

Authors:  Giancarlo Marra; Marco Oderda; Giorgio Calleris; Alessandro Marquis; Federica Peretti; Andrea Zitella; Marco Moschini; Rafael Sanchez-Salas; Robert Jeffrey Karnes; Burkhard Kneitz; Martin Spahn; Donatella Pacchioni; Paolo Gontero
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Review 5.  Incorporation of tissue-based genomic biomarkers into localized prostate cancer clinics.

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  5 in total

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