首都医科大学学报 ›› 2019, Vol. 40 ›› Issue (1): 72-77.doi: 10.3969/j.issn.1006-7795.2019.01.013

• 泌尿系统肿瘤:基础研究与临床实践 • 上一篇    下一篇

TMPRSS2-ERG融合基因在淋巴结转移前列腺癌中的阳性率及与生存的关系

谢英伟, 金世鹏, 闫伟, 王伟, 平浩, 刘跃新   

  1. 首都医科大学附属北京同仁医院泌尿外科, 北京 100730
  • 收稿日期:2018-10-24 出版日期:2019-01-21 发布日期:2019-01-23
  • 通讯作者: 刘跃新 E-mail:doctorlyx@126.com
  • 基金资助:
    北京市自然科学基金(7102033)。

Prevalence and prognostic significance of TMPRSS2-ERG fusion gene in prostate cancer with lymph node metastasis

Xie Yingwei, Jin Shipeng, Yan Wei, Wang Wei, Ping Hao, Liu Yuexin   

  1. Department of Urology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
  • Received:2018-10-24 Online:2019-01-21 Published:2019-01-23
  • Supported by:
    This study was supported by Natural Science Foundation of Beijing (7102033)。

摘要: 目的 研究TMPRSS2-ERG融合基因在淋巴结阳性前列腺癌中的分布以及对其预后的意义。方法 收集2008年1月至2012年12月前列腺癌根治术后,术后病理提示淋巴结转移的标本50例。所有患者术后均接受内分泌治疗。利用荧光原位杂交技术检测标本中TMPRSS2-ERG融合基因。收集患者各种肿瘤特征(Gleason评分、分期)、有无生化复发、疾病特异性和总体生存率。比较融合基因阳性和阴性患者的临床病理资料分布及预后差异。结果 19例(38%)原发性肿瘤中检测到TMPRSS2-ERG融合基因。转移淋巴结中有16例(32%)出现融合基因。原发肿瘤与转移灶TMPRSS2-ERG状态一致性较好(Kappa=0.73)。在COX分析中,原发肿瘤中TMPRSS2-ERG融合基因与Gleason评分是生化复发的预测因素。在生存分析中,原发肿瘤/淋巴结融合基因(+/+)组与原发肿瘤/淋巴结融合基因(+/-)组预后低于原发肿瘤/淋巴结融合基因(-/-)组,无生化复发率差异存在统计学意义(P=0.03)。结论 TMPRSS2-ERG融合基因在伴有淋巴结转移的原发性前列腺癌中阳性率38%。原发肿瘤与淋巴结转移灶中TMPRRS2-ERG融合基因具有较好的一致性。原发肿瘤TMPRSS2-ERG融合基因阳性的患者预后较差。

关键词: TMPRSS2-ERG融合基因, 前列腺癌, 转移, 生存期

Abstract: Objective To investigate the distribution and prognostic significance of TMPRSS2-ERG fusion gene in lymph node-positive prostate cancer. Methods Fifty cases of lymph node metastasis after radical prostatectomy from January 2008 to December 2012 were collected. All patients received endocrine therapy after operation. The TMPRRS2-ERG fusion gene was detected with fluorescence in situ hybridization. The data were correlated with various tumor features (Gleason score, stage) and biochemical recurrence-free, disease-specificity, and overall survival. The distribution of clinicopathological data and prognosis of patients were compared with each other for the patients with positive and negative fusion genes. Results The TMPRSS2-ERG fusion gene was detected in 19 cases (38%) of the primary tumors. Fusion genes were present in 16 cases (32%) of the metastatic lymph nodes. The primary tumor and metastatic lesion TMPRSS2-ERG status was in good agreement (Kappa=0.73). The TMPRSS2-ERG fusion gene and Gleason score in primary tumors in COX analysis were predictors of biochemical recurrence. In survival analysis, the prognosis of primary tumors/lymph node fusion gene (+/+) group and primary tumors/lymph node fusion gene (+/-) group was lower than that of primary tumors/lymph node fusion gene (-/-) group, with significant difference in the non-biochemical recurrence rate (P=0.03). Conclusion The positive rate of TMPRSS2-ERG fusion gene in primary prostate cancer with lymph node metastasis was 38%. The fusion gene of TMPRRS2-ERG in primary tumors and lymph node metastases had good consistency (Kappa=0.73). Patients with positive primary tumor TMPRSS2-ERG fusion gene have a poor prognosis.

Key words: TMPRSS2-ERG, prostate cancer, metastases, survival

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