TY - JOUR
T1 - Validation of tertiary Gleason pattern 5 in Gleason score 7 prostate cancer as an independent predictor of biochemical recurrence and development of a prognostic model
AU - Lucca, Ilaria
AU - Shariat, Shahrokh F.
AU - Briganti, Alberto
AU - Lotan, Yair
AU - Roehrborn, Claus
AU - Montorsi, Francesco
AU - Remzi, Mesut
AU - Seitz, Christian
AU - Fajkovic, Harun
AU - Klingler, Christoph
AU - Karakiewicz, Pierre I.
AU - Sun, Maxine
AU - Rouprêt, Morgan
AU - Loidl, Wolfgang
AU - Pummer, Karl
AU - Klatte, Tobias
N1 - Funding Information:
I.L. is supported by the development fund of the CHUV-University Hospital . T.K. is supported by funds of the Oesterreichische Nationalbank (Anniversary Fund, Project no.: 15362 ).
Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Objective: To validate the biological and prognostic value of tertiary Gleason pattern 5 (TGP5) in patients with Gleason score 7 (GS 7) prostate cancer (PCa) and to develop a prognostic model to identify the high-risk group of patients with TGP5. Material and methods: We retrospectively reviewed the data from 4,146 patients with localized (pT2-3 N0 M0) GS 7 PCa treated by radical prostatectomy (RP) without adjuvant therapy. The primary end point was biochemical recurrence (BCR), and the secondary one was to build a bootstrap-corrected multivariable Cox model. Results: Of the 4,146 patients, 416 (10%) had a TPG5 in the RP specimen. TGP5 was associated with BCR in both univariable and multivariable analyses that adjusted for the effects of standard pathological features (P<0.001). A prognostic model based on preoperative prostate-specific antigen levels (<10 vs.≥10. ng/ml), primary and secondary Gleason pattern (3+4 vs. 4+3), pathological tumor category (pT2/pT3a vs. pT3b), and surgical margin status (R0 vs. R+) stratified patients with a discrimination of 72.2%. Patients in the low-risk group had a 5-year BCR-free survival rate of 76.3% compared with only 18.5% for those in the high-risk group (P<0.001). Conclusions: Knowledge of TGP5 improves our prognostication of patients with GS 7 PCa treated with RP. We developed a statistical tool to help identify the patients with TGP5 who are at the highest risk of BCR after RP, thereby helping with the clinical decision making regarding adjuvant trials and follow-up scheduling.
AB - Objective: To validate the biological and prognostic value of tertiary Gleason pattern 5 (TGP5) in patients with Gleason score 7 (GS 7) prostate cancer (PCa) and to develop a prognostic model to identify the high-risk group of patients with TGP5. Material and methods: We retrospectively reviewed the data from 4,146 patients with localized (pT2-3 N0 M0) GS 7 PCa treated by radical prostatectomy (RP) without adjuvant therapy. The primary end point was biochemical recurrence (BCR), and the secondary one was to build a bootstrap-corrected multivariable Cox model. Results: Of the 4,146 patients, 416 (10%) had a TPG5 in the RP specimen. TGP5 was associated with BCR in both univariable and multivariable analyses that adjusted for the effects of standard pathological features (P<0.001). A prognostic model based on preoperative prostate-specific antigen levels (<10 vs.≥10. ng/ml), primary and secondary Gleason pattern (3+4 vs. 4+3), pathological tumor category (pT2/pT3a vs. pT3b), and surgical margin status (R0 vs. R+) stratified patients with a discrimination of 72.2%. Patients in the low-risk group had a 5-year BCR-free survival rate of 76.3% compared with only 18.5% for those in the high-risk group (P<0.001). Conclusions: Knowledge of TGP5 improves our prognostication of patients with GS 7 PCa treated with RP. We developed a statistical tool to help identify the patients with TGP5 who are at the highest risk of BCR after RP, thereby helping with the clinical decision making regarding adjuvant trials and follow-up scheduling.
KW - Biochemical recurrence
KW - Gleason 7
KW - Prostate cancer
KW - Risk-stratification model
KW - Tertiary Gleason pattern 5
UR - http://www.scopus.com/inward/record.url?scp=84923338699&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84923338699&partnerID=8YFLogxK
U2 - 10.1016/j.urolonc.2014.08.011
DO - 10.1016/j.urolonc.2014.08.011
M3 - Article
C2 - 25443275
AN - SCOPUS:84923338699
SN - 1078-1439
VL - 33
SP - 71.e21-71.e26
JO - Urologic Oncology: Seminars and Original Investigations
JF - Urologic Oncology: Seminars and Original Investigations
IS - 2
ER -