Journal of Capital Medical University ›› 2020, Vol. 41 ›› Issue (1): 103-107.doi: 10.3969/j.issn.1006-7795.2020.01.020

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Correlation between TMPRSS2-ERG fusion gene and survival rate of metastatic castration-resistant prostate cancer after chemotherapy

Xie Yingwei, Jin Shipeng, Li Shuang, Wang Yonghui, Wang Wei, Ping Hao, Liu Yuexin   

  1. Department of Urology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
  • Received:2019-06-11 Online:2020-02-21 Published:2020-02-13
  • Supported by:
    This study was supported by Natural Science Foundation of Beijing (7102033).

Abstract: Objective To determine the correlation of TMPRSS2-ERG(T-E) fusion gene to the survival rate in metastatic castration-resistant prostate cancer after docetaxel chemotherapy. Methods We included 20 patients with benign prostatic hyperplasia and 50 patients with prostate cancer(mCRPC) chemotherapy. The expression of T-E fusion gene in peripheral blood mononuclear cells was examined by quantitative real time polymerase chain reaction(qRT-PCR). Therapeutic responses of patients with different fusion gene expression were assessed by prostate specific antigen (PSA) response rate, PSA-progression free survival(PFS), radiological progression free survival(RX-PFS), and overall survival(OS). Results The T-E fusion gene was detected in 10 (20%) of 50 prostate cancer patients. The PSA response rate in the T-E positive group was lower than that in the negative group (32.52% vs 74.35%, P=0.040). Univariate survival analysis showed that PSA-PFS, RX-PFS, and OS were lower in T-E positive patients than in negative patients, and the difference was statistically significant (P<0.01). Multivariate Cox regression analysis showed that T-E positive was an independent risk factor for PSA-PFS, RX-PFS and OS (P=0.010, P=0.010, P=0.020). Conclusion This study demonstrates that T-E fusion gene expression is an independent risk factor for PSA-PFS, RX-PFS and OS in mCRPC patients treated with docetaxel.

Key words: TMPRSS2-ERG fusion gene, prostate cancer, chemotherapy, drug resistance

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