Prognostic value of intraductal carcinoma of the prostate in radical prostatectomy specimens

被引:140
作者
Kimura, Kyosuke [1 ]
Tsuzuki, Toyonori [2 ]
Kato, Masashi [3 ]
Saito, Akiko M. [4 ]
Sassa, Naoto [3 ]
Ishida, Ryo [5 ]
Hirabayashi, Hiroki [6 ]
Yoshino, Yasushi [3 ]
Hattori, Ryohei [7 ]
Gotoh, Momokazu [3 ]
机构
[1] Natl Hosp Org, Nagoya Med Ctr, Dept Urol, Nagoya, Aichi, Japan
[2] Japanese Red Cross Nagoya Daini Hosp, Dept Pathol, Nagoya, Aichi 4668650, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Urol, Nagoya, Aichi 4648601, Japan
[4] Nalt Hosp Org, Nagoya Med Ctr, Clin Res Ctr, Dept Clin Res Promot,Lab Clin Epidemiol & Hlth Se, Nagoya, Aichi, Japan
[5] Japanese Red Cross Nagoya Daini Hosp, Dept Urol, Nagoya, Aichi 4668650, Japan
[6] Komaki City Hosp, Dept Urol, Komaki, Japan
[7] Japanese Red Cross Nagoya Daiichi Hos, Dept Urol, Nagoya, Aichi, Japan
关键词
cancer-specific survival; radical prostatectomy; clinical outcome; prostate cancer; clinical progression-free survival; intraductal carcinoma of the prostate; 2005; INTERNATIONAL-SOCIETY; CANCER-SPECIFIC MORTALITY; INTRAEPITHELIAL NEOPLASIA; ADENOCARCINOMA; PROGRESSION; IMPACT; PATTERNS; SURVIVAL; ANTIGEN; SPREAD;
D O I
10.1002/pros.22786
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Intraductal carcinoma of the prostate (IDC-P) is an adverse prognostic factor for radical prostatectomy (RP). The endpoint in most IDC-P studies is increased prostate-specific antigen (PSA) levels. The aim of this study was to evaluate whether IDC-P in RP specimens is an adverse prognostic factor for progression-free survival (PFS) and cancer-specific survival (CSS). METHODS We retrospectively evaluated 206 high-risk prostate cancer patients treated with RP and analyzed data on age, serum PSA level at diagnosis, biopsy Gleason score (bGS), surgical margin (SM), clinical T stage (cT), extraprostatic extension (EPE), seminal vesicle invasion (SVI), lymph node metastasis (LN), and neoadjuvant therapy. RESULTS An IDC-P component was found in 104 cases. Forty-four patients experienced clinical failure, and 20 patients died of the disease. Patients with IDC-P showed a higher bGS and stage (including cT, EPE, SVI, and LN) than those without IDC-P. In univariate analysis, IDC-P, PSA level, bGS, SM, cT, SVI, LN, and EPE (P < 0.0001) were significantly associated with PFS. IDC-P (P = 0.0004), PSA level (P < 0.0001), SM (P = 0.0013), cT (P = 0.0019), SVI (P = 0.0012), and LN (P = 0.0002) were significantly associated with CSS. In multivariate analysis, IDC-P (P = 0.0038), and cT (P = 0.0001) were significantly associated with PFS. IDC-P (P = 0.0238) and PSA level (P = 0.0112) were significantly associated with CSS. CONCLUSIONS IDC-P in RP specimens was an independent risk factor for PFS and CSS and could predict clinical outcomes. Prostate 74:680-687, 2014. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:680 / 687
页数:8
相关论文
共 34 条
[1]   Radical Prostatectomy versus Watchful Waiting in Early Prostate Cancer [J].
Bill-Axelson, Anna ;
Holmberg, Lars ;
Ruutu, Mirja ;
Garmo, Hans ;
Stark, Jennifer R. ;
Busch, Christer ;
Nordling, Stig ;
Haggman, Michael ;
Andersson, Swen-Olof ;
Bratell, Stefan ;
Spangberg, Anders ;
Palmgren, Juni ;
Steineck, Gunnar ;
Adami, Hans-Olov ;
Johansson, Jan-Erik .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (18) :1708-1717
[2]   Postoperative radiotherapy after radical prostatectomy for high-risk prostate cancer: long-term results of a randomised controlled trial (EORTC trial 22911) [J].
Bolla, Michel ;
van Poppel, Hein ;
Tombal, Bertrand ;
Vekemans, Kris ;
Da Pozzo, Luigi ;
de Reijke, Theo M. ;
Verbaeys, Antony ;
Bosset, Jean-Francois ;
van Velthoven, Roland ;
Colombel, Marc ;
van de Beek, Cees ;
Verhagen, Paul ;
van den Bergh, Alphonsus ;
Sternberg, Cora ;
Gasser, Thomas ;
van Tienhoven, Geertjan ;
Scalliet, Pierre ;
Haustermans, Karin ;
Collette, Laurence .
LANCET, 2012, 380 (9858) :2018-2027
[3]   Intraductal carcinoma of the prostate: Precursor or aggressive phenotype of prostate cancer? [J].
Bonkhoff, Helmut ;
Wheeler, Thomas M. ;
van der Kwast, Theodorus H. ;
Magi-Galluzzi, Cristina ;
Montironi, Rodolfo ;
Cohen, Ronald J. .
PROSTATE, 2013, 73 (04) :442-448
[4]   Impact of surgical margin status on prostate-cancer-specific mortality [J].
Chalfin, Heather J. ;
Dinizo, Michael ;
Trock, Bruce J. ;
Feng, Zhaoyong ;
Partin, Alan W. ;
Walsh, Patrick C. ;
Humphreys, Elizabeth ;
Han, Misop .
BJU INTERNATIONAL, 2012, 110 (11) :1684-1689
[5]  
Cohen RJ, 2000, PROSTATE, V43, P11, DOI 10.1002/(SICI)1097-0045(20000401)43:1<11::AID-PROS3>3.0.CO
[6]  
2-B
[7]   Prostate-specific antigen (PSA) as a surrogate end point for survival in prostate cancer clinical trials [J].
Collette, Laurence .
EUROPEAN UROLOGY, 2008, 53 (01) :6-9
[8]   Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer [J].
D'Amico, AV ;
Whittington, R ;
Malkowicz, SB ;
Schultz, D ;
Blank, K ;
Broderick, GA ;
Tomaszewski, JE ;
Renshaw, AA ;
Kaplan, I ;
Beard, CJ ;
Wein, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (11) :969-974
[9]  
Dawkins HJS, 2000, PROSTATE, V44, P265
[10]   Impact on the Clinical Outcome of Prostate Cancer by the 2005 International Society of Urological Pathology Modified Gleason Grading System [J].
Dong, Fei ;
Wang, Chaofu ;
Farris, A. Brad ;
Wu, Shulin ;
Lee, Hang ;
Olumi, Aria F. ;
McDougal, W. Scott ;
Young, Robert H. ;
Wu, Chin-Lee .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2012, 36 (06) :838-843