Prior-cancer diagnosis in men with nonmetastatic prostate cancer and the risk of prostate-cancer-specific and all-cause mortality.

ISRN oncology Pub Date : 2014-01-30 eCollection Date: 2014-01-01 DOI:10.1155/2014/736163
Kristina Mirabeau-Beale, Ming-Hui Chen, Anthony V D'Amico
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引用次数: 6

Abstract

Purpose. We evaluated the impact a prior cancer diagnosis had on the risk of prostate-cancer-specific mortality (PCSM) and all-cause mortality (ACM) in men with PC. Methods. Using the SEER data registry, 166,104 men (median age: 66) diagnosed with PC between 2004 and 2007 comprised the study cohort. Competing risks and Cox regression were used to evaluate whether a prior cancer diagnosis impacted the risk of PCSM and ACM adjusting for known prognostic factors PSA level, age at and year of diagnosis, race, and whether PC treatment was curative, noncurative, or active surveillance (AS)/watchful waiting (WW). Results. At a median followup of 2.75 years, 12,453 men died: 3,809 (30.6%) from PC. Men with a prior cancer were followed longer, had GS 8 to 10 PC more often, and underwent WW/AS more frequently (P < 0.001). Despite these differences that should increase the risk of PCSM, the adjusted risk of PCSM was significantly decreased (AHR: 0.66 (95% CI: (0.45, 0.97); P = 0.033), while the risk of ACM was increased (AHR: 2.92 (95% CI: 2.64, 3.23); P < 0.001) in men with a prior cancer suggesting that competing risks accounted for the reduction in the risk of PCSM. Conclusion. An assessment of the impact that a prior cancer has on life expectancy is needed at the time of PC diagnosis to determine whether curative treatment for unfavorable-risk PC versus AS is appropriate.

Abstract Image

男性非转移性前列腺癌的既往癌症诊断与前列腺癌特异性和全因死亡率的风险
目的。我们评估了既往癌症诊断对前列腺癌患者前列腺癌特异性死亡率(PCSM)和全因死亡率(ACM)风险的影响。方法。使用SEER数据注册表,2004年至2007年间诊断为PC的166104名男性(中位年龄:66岁)组成了研究队列。使用竞争风险和Cox回归来评估先前的癌症诊断是否影响PCSM和ACM的风险,调整已知的预后因素PSA水平,诊断年龄和年份,种族,以及PC治疗是否有效,无疗效,或主动监测(AS)/观察等待(WW)。结果。在平均2.75年的随访中,12,453人死亡:3,809人(30.6%)死于前列腺癌。既往有癌症的男性随访时间更长,GS 8 - 10 PC的频率更高,WW/AS的频率更高(P < 0.001)。尽管这些差异会增加PCSM的风险,但PCSM的调整风险显著降低(AHR: 0.66 (95% CI: 0.45, 0.97);P = 0.033),而发生ACM的风险增加(AHR: 2.92 (95% CI: 2.64, 3.23);P < 0.001),表明竞争风险是PCSM风险降低的原因。结论。在PC诊断时,需要评估既往癌症对预期寿命的影响,以确定治疗不良风险PC与AS是否合适。
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