Low-molecular-weight protein tyrosine phosphatase expression as a prognostic factor for men with metastatic hormone-naive prostate cancer

被引:7
作者
Ohtaka, Mari [1 ,2 ]
Miyoshi, Yasuhide [1 ,2 ]
Kawahara, Takashi [1 ,2 ]
Ohtake, Shinji [1 ,2 ]
Yasui, Masato [1 ,2 ]
Uemura, Koichi [1 ,2 ]
Yoneyama, Shuko [1 ,2 ]
Hattori, Yusuke [1 ,2 ]
Teranishi, Jun-ichi [1 ,2 ]
Yokomizo, Yumiko [1 ,2 ]
Uemura, Hiroji [1 ,2 ]
Miyamoto, Hiroshi [3 ]
Yao, Masahiro [1 ,2 ]
机构
[1] Yokohama City Univ, Med Ctr, Dept Urol, Yokohama, Kanagawa, Japan
[2] Yokohama City Univ, Med Ctr, Dept Renal Transplantat, Yokohama, Kanagawa, Japan
[3] Univ Rochester, Med Ctr, Dept Pathol & Lab Med, Rochester, NY 14642 USA
关键词
Low-molecular-weight protein tyrosine phosphatase; Metastatic hormone-naive prostate cancer; Biomarker; RECEPTOR; SURVIVAL; GROWTH;
D O I
10.1016/j.urolonc.2017.05.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Recent studies have demonstrated that up-front docetaxel combined with androgen deprivation therapy (ADT) prolongs survival in some patients with metastatic hormone-naive prostate cancer (mHNPC). However, new biomarkers for selecting personalized treatment strategies for mHNPC are warranted. We evaluated the value of low-molecular-weight protein tyrosine phosphatase (LMW-PTP) expression as a prognosticator in men with mHNPC. Methods and materials: A total of 48 men with mHNPC diagnosed from 2003 to 2009 were enrolled in this study. Prostate cancer tissues obtained by needle biopsies were immunohistochemically stained for LMW-PTP. Correlations between LMW-PTP expression and clinicopathological characteristics were then assessed. Results: At the time of analysis, 29 (60.4%) patients were alive, whereas 15 (31.3%) and 4 (8.3%) died of prostate cancer and nonprostate cancer, respectively. Of these, 29 (60.4%) had low LMW-PTP expression and 19 (39.6%) had high expression. Median overall survival (OS) for patients with high LMW-PTP expression was not reached and that for patients with low LMW-PTP expression was 23.8 months. High LMW-PTP expression was significantly correlated with a shorter OS compared with low LMW-PTP expression (P = 0.01). Moreover, multivariate analysis showed that Gleason score (>= 8 vs. <= 7; HR = 5.8, 95% CI: 1.3-26.5, P = 0.02) and LMW-PTP expression (high vs. low; HR = 2.7, 95% CI: 1.0-7.2, P = 0.04) were independent prognostic factors for OS. Conclusions: LMW-PTP is a potential biomarker to predict OS in patients with mHNPC. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:607.e9 / 607.e14
页数:6
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