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较高的前列腺特异性抗原水平预示着患有骨转移且血清碱性磷酸酶正常的激素难治性前列腺癌患者的生存率会提高。

Higher prostate-specific antigen levels predict improved survival in patients with hormone-refractory prostate cancer who have skeletal metastases and normal serum alkaline phosphatase.

作者信息

Xie Wanling, Nakabayashi Mari, Regan Meredith M, Oh William K

机构信息

Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cancer. 2007 Dec 15;110(12):2709-15. doi: 10.1002/cncr.23111.

Abstract

BACKGROUND

Higher prostate-specific antigen (PSA) and alkaline phosphatase (ALK-P) levels predicted worse survival in men with metastatic hormone-refractory prostate cancer (HRPC). In the current study, the authors evaluated the combined effects of PSA and ALK-P on survival.

METHODS

Two hundred twenty-four men who had HRPC with bone metastases and who were receiving chemotherapy were identified, and 143 of those men had data available on both ALK-P and PSA levels at chemotherapy initiation. The primary endpoint of the study was overall survival (OS) after chemotherapy. The men were dichotomized into normal and abnormal ALK-P groups according to levels based on institutional normal ranges. The effect of PSA was evaluated as both a categorical value and a continuous value using Cox regression.

RESULTS

Eighty-nine of 143 patients (62%) had elevated ALK-P levels. The median PSA was 147 ng/mL (93 ng/mL in patients with normal ALK-P, 171 ng/mL in patients with elevated ALK-P). At a median follow-up of 30 months after chemotherapy initiation, 93 patients had died. The median OS after chemotherapy was 15.8 months (95% confidence interval, 12.8-18.4 months) and was significantly longer if ALK-P was in the normal range (21.3 months vs 14 months; P = .005). For the group with normal ALK-P levels, the median OS was 12.5 months, 24.5 months, and 36.9 months for patients with low, medium, and high PSA levels, respectively. In contrast, the effect of PSA on survival was not as evident in the group with elevated ALK-P levels (16.5 months vs 11.9 months vs 12.1 months, respectively; P = .14 for interaction). Age-adjusted multivariate analysis demonstrated statistically significant interactions of PSA and ALK-P with OS (P = .02).

CONCLUSIONS

ALK-P significantly predicted OS in men with HRPC who had bone metastases. In patients with normal ALK-P levels, higher PSA levels were associated with improved survival.

摘要

背景

较高的前列腺特异性抗原(PSA)和碱性磷酸酶(ALK-P)水平预示着转移性激素难治性前列腺癌(HRPC)男性患者的生存预后较差。在本研究中,作者评估了PSA和ALK-P对生存的联合影响。

方法

确定了224例患有HRPC并伴有骨转移且正在接受化疗的男性患者,其中143例患者在化疗开始时同时有ALK-P和PSA水平的数据。研究的主要终点是化疗后的总生存期(OS)。根据机构正常范围的水平,将这些男性患者分为ALK-P正常组和异常组。使用Cox回归将PSA作为分类值和连续值来评估其影响。

结果

143例患者中有89例(62%)ALK-P水平升高。PSA的中位数为147 ng/mL(ALK-P正常的患者为93 ng/mL,ALK-P升高的患者为171 ng/mL)。化疗开始后的中位随访时间为30个月,93例患者死亡。化疗后的中位OS为15.8个月(95%置信区间,12.8 - 18.4个月),如果ALK-P在正常范围内,则明显更长(21.3个月对14个月;P = 0.005)。对于ALK-P水平正常的组,PSA水平低、中、高的患者的中位OS分别为12.5个月、24.5个月和36.9个月。相比之下,在ALK-P水平升高的组中,PSA对生存的影响不那么明显(分别为16.5个月对11.9个月对12.1个月;交互作用P = 0.14)。年龄调整后的多变量分析显示PSA和ALK-P与OS之间存在统计学上显著的交互作用(P = 0.02)。

结论

ALK-P显著预测了患有骨转移的HRPC男性患者的OS。在ALK-P水平正常的患者中,较高的PSA水平与更好的生存相关。

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