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多西他赛联合唑来膦酸及泼尼松用于激素难治性前列腺癌的化疗:预测疗效及生存的因素

Docetaxel-based chemotherapy with zoledronic acid and prednisone in hormone refractory prostate cancer: factors predicting response and survival.

作者信息

Nayyar Rishi, Sharma Nitin, Gupta Narmada P

机构信息

Department of Urology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Int J Urol. 2009 Sep;16(9):726-31. doi: 10.1111/j.1442-2042.2009.02351.x.

Abstract

OBJECTIVES

To evaluate the efficacy of docetaxel/prednisone and zoledronic acid in hormone refractory prostate cancer (HRPC) patients and to analyze prognostic factors predicting overall survival.

METHODS

Forty-four HRPC patients were given docetaxel (75 mg/m(2)), prednisone and zoledronic acid (4 mg) every three weeks. Overall and progression-free survival curves were calculated. Using the log-rank test, variables predicting overall survival (age, Gleason score, baseline prostate-specific antigen [PSA], percentage PSA decline, nadir PSA, number of chemotherapy cycles) were calculated.

RESULTS

Median age was 66 years and mean PSA 171.25 ng/mL. The average number of given cycles was 6.3. A good PSA response (>50% decline) was observed in 26/44 cases (59.1%). A total of 17/44 (38.6%) patients expired with a median overall survival of 62.4 weeks. Patients with a Gleason score less than 7, who received more than four cycles and with a more-than-50% decline in PSA had significantly better survival. Variables like age, baseline PSA and nadir PSA did not significantly affect survival.

CONCLUSION

The combination of docetaxel/zoledronic/prednisone is safe and effective in the management of HRPC. Patients with a Gleason score <7, PSA decline >50% and those who receive more than four cycles have significantly better survival.

摘要

目的

评估多西他赛/泼尼松和唑来膦酸对激素难治性前列腺癌(HRPC)患者的疗效,并分析预测总生存期的预后因素。

方法

44例HRPC患者每三周接受多西他赛(75mg/m²)、泼尼松和唑来膦酸(4mg)治疗。计算总生存期和无进展生存期曲线。使用对数秩检验计算预测总生存期的变量(年龄、Gleason评分、基线前列腺特异性抗原[PSA]、PSA下降百分比、最低PSA、化疗周期数)。

结果

中位年龄为66岁,平均PSA为171.25ng/mL。平均给药周期数为6.3个。26/44例(59.1%)观察到良好的PSA反应(下降>50%)。共有17/44例(38.6%)患者死亡,中位总生存期为62.4周。Gleason评分小于7、接受超过四个周期治疗且PSA下降超过50%的患者生存期明显更长。年龄、基线PSA和最低PSA等变量对生存期无显著影响。

结论

多西他赛/唑来膦酸/泼尼松联合用药治疗HRPC安全有效。Gleason评分<7、PSA下降>50%且接受超过四个周期治疗的患者生存期明显更长。

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