Teoh Jeremy Yuen Chun, Tsu James Hok Leung, Yuen Steffi Kar Kei, Chan Samson Yun Sang, Chiu Peter Ka Fung, Lee Wai-Man, Wong Ka-Wing, Ho Kwan-Lun, Hou Simon See Ming, Ng Chi-Fai, Yiu Ming-Kwong
Division of Urology, Department of Surgery, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, China.
Ann Surg Oncol. 2015 Apr;22(4):1385-91. doi: 10.1245/s10434-014-4105-8. Epub 2014 Sep 19.
This study investigated the prognostic significance of time to the prostate-specific antigen nadir (TTPN) and its relationship to survival beyond TTPN in metastatic prostate cancer after primary androgen-deprivation therapy (ADT).
All metastatic prostate cancer patients treated with primary ADT from 2000 to 2009 were reviewed. The prognostic significance of TTPN in predicting progression-free survival (PFS) beyond TTPN and overall survival (OS) beyond TTPN was analyzed using the Cox regression model. The median PFS and OS were plotted against TTPN on a monthly interval. The PFS beyond TTPN and the OS beyond TTPN with reference to TTPN were calculated and presented.
The study enrolled 419 patients with a median follow-up period of 38 months. The findings showed that TTPN was a significant prognostic indicator for both PFS beyond TTPN (hazard ratio [HR] 0.72, 95 % confidence interval [CI] 0.52-0.99, p = 0.04) and OS beyond TTPN (HR 0.65, 95 % CI 0.47-0.90, p = 0.01) according to Cox regression analyses. The relationship between TTPN and survival beyond TTPN consisted of three phases. In the first phase (<3 months for PFS and <6 months for OS), the survival beyond TTPN increased with TTPN. In the second phase (3-17 months for PFS and 6-20 months for OS), the survival beyond TTPN remained relatively static. In the third phase (>17 months for PFS and >20 months for OS), the survival beyond TTPN increased exponentially with TTPN.
In this study, TTPN was a good prognostic indicator for PFS beyond TTPN and OS beyond TTPN in metastatic prostate cancer cases after primary ADT. Different TTPNs had different implications for predicting survival beyond TTPN.
本研究调查了前列腺特异性抗原最低点时间(TTPN)的预后意义及其与转移性前列腺癌初次雄激素剥夺治疗(ADT)后TTPN之外生存期的关系。
回顾了2000年至2009年接受初次ADT治疗的所有转移性前列腺癌患者。使用Cox回归模型分析TTPN在预测TTPN之后的无进展生存期(PFS)和总生存期(OS)方面的预后意义。将PFS和OS的中位数按月间隔与TTPN绘制在一起。计算并呈现了参照TTPN的TTPN之后的PFS和TTPN之后的OS。
该研究纳入了419例患者,中位随访期为38个月。研究结果显示,根据Cox回归分析,TTPN是TTPN之后PFS(风险比[HR] 0.72,95%置信区间[CI] 0.52 - 0.99,p = 0.04)和TTPN之后OS(HR 0.65,95% CI 0.47 - 0.90,p = 0.01)的显著预后指标。TTPN与TTPN之后生存期的关系包括三个阶段。在第一阶段(PFS < 3个月且OS < 6个月)中,TTPN之后的生存期随TTPN增加。在第二阶段(PFS为3 - 17个月且OS为6 - 20个月)中,TTPN之后的生存期保持相对稳定。在第三阶段(PFS > 17个月且OS > 20个月)中,TTPN之后的生存期随TTPN呈指数增长。
在本研究中,TTPN是转移性前列腺癌初次ADT后TTPN之后PFS和TTPN之后OS的良好预后指标。不同的TTPN对预测TTPN之后的生存期有不同的意义。