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

被引:139
|
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
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