Yamada Yoshiaki, Naruse Katsuya, Nakamura Kogenta, Taki Tomohiro, Tobiume Motoi, Zennami Kenji, Nishikawa Genya, Itoh Youko, Muramatsu Yoshitaka, Nanaura Hiroshi, Nishimura Miho, Takii Kazuko, Adham Adnan Odhafa Kh, Honda Nobuaki
Department of Urology, Aichi Medical University School of Medicine;
Exp Ther Med. 2010 Jul;1(4):635-639. doi: 10.3892/etm_00000099. Epub 2010 Jul 1.
It has not yet been determined whether certain types of prostate cancer with bone metastasis (M1b PC) are associated with a poor outcome. The present study retrospectively assessed the potential significance of various clinical data in predicting the outcome of M1b PC. The subjects were 104 patients who attended our hospital and received a diagnosis of M1b PC between January 1998 and December 2006. The age of the subjects ranged from 51 to 91 years (median 74). The observation period ranged from 4 to 122 months (median 43). The parameters investigated were T classification, N classification, Gleason score (GS), pre-treatment prostate-specific antigen (PSA) level, extent of disease (EOD) grade, alkaline phosphatase (ALP), lactate dehydrogenase (LDH), calcium and hemoglobin (Hb) levels and platelet count. The 5-year cause-specific survival rate was 56.6% and the 10-year cause-specific survival rate was 34.9%. Log-rank test and Cox univariate analysis identified the following factors with statistically significant differences: pre-treatment PSA level ≥192, N1, GS ≥8, EOD grade 3+4, high LDH, high ALP and low Hb. Multivariate Cox proportional hazard analysis identified the factors GS ≥8 and high LDH with significant differences. The hazard ratio was 4.967 and 2.728, respectively, and the probability value (P) was 0.029 and 0.004, respectively. When the subjects with GS ≥8 and high LDH were classified as the high-risk group, the 5-year cause-specific survival rate was 24.6%. The outcome was significantly poorer in this group (P<0.0001) than in the other group, which had a 5-year cause-specific survival rate of 67.7%. The present study showed that patients with M1b PC with GS ≥8 and high LDH have a very poor outcome and thus should be treated as a high-risk group requiring close follow-up.
某些伴有骨转移的前列腺癌(M1b PC)类型是否与不良预后相关尚未确定。本研究回顾性评估了各种临床数据在预测M1b PC预后方面的潜在意义。研究对象为1998年1月至2006年12月期间在我院就诊并被诊断为M1b PC的104例患者。研究对象的年龄在51岁至91岁之间(中位数为74岁)。观察期为4个月至122个月(中位数为43个月)。所研究的参数包括T分期、N分期、 Gleason评分(GS)、治疗前前列腺特异性抗原(PSA)水平、疾病范围(EOD)分级、碱性磷酸酶(ALP)、乳酸脱氢酶(LDH)、钙和血红蛋白(Hb)水平以及血小板计数。5年病因特异性生存率为56.6%,10年病因特异性生存率为34.9%。对数秩检验和Cox单因素分析确定了以下具有统计学显著差异的因素:治疗前PSA水平≥192、N1、GS≥8、EOD分级3 + 4、高LDH、高ALP和低Hb。多因素Cox比例风险分析确定GS≥8和高LDH因素具有显著差异。风险比分别为4.967和2.728,概率值(P)分别为0.029和0.004。当将GS≥8和高LDH的研究对象归为高危组时,5年病因特异性生存率为24.6%。该组的预后明显比另一组差(P<0.0001),另一组的5年病因特异性生存率为67.7%。本研究表明,GS≥8和高LDH的M1b PC患者预后非常差,因此应作为需要密切随访的高危组进行治疗。