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多西他赛是治疗皮质类固醇难治性前列腺癌的重要选择。

Docetaxel as a vital option for corticosteroid-refractory prostate cancer.

机构信息

Department of Urology, The University of Tokyo Hospital, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-8655, Japan.

出版信息

Int Urol Nephrol. 2011 Dec;43(4):1081-7. doi: 10.1007/s11255-011-9922-0. Epub 2011 Mar 11.

Abstract

OBJECTIVES

The efficacy of docetaxel (TAX) chemotherapy for corticosteroid-refractory refractory prostate cancer (CRPC) is uncertain.

MATERIALS AND METHODS

We retrospectively reviewed outcomes of 51 men with corticosteroid-refractory CRPC treated at our institute. Of them, 24 men had received only dexamethasone (DEX) before the approval of TAX (historical control). The remaining 27 men who had already become DEX refractory on the approval of TAX underwent TAX plus DEX.

RESULTS

The median overall survival for men treated with TAX plus DEX (17.6 months) was significantly longer than men with DEX (8.1 months, P = 0.021). On univariate analysis, performance status, lactate dehydrogenase (LDH), alkaline phosphatase (ALP), prostate specific antigen (PSA), and TAX therapy were significant factors for overall survival. Of these, performance status and TAX therapy remained as the significant factor on multivariate analysis. No significant benefit was detected for men with advanced disease such as poorer performance status, elevated LDH, elevated ALP, or high PSA. Grades 3, 4 toxicities including anemia (19%), leukocytopenia (26%), and neutropenia (26%) were found in TAX cases.

CONCLUSIONS

Our results suggest that TAX would be a vital option for DEX refractory CRPC possibly with more efficacy for less advanced stages.

摘要

目的

多西他赛(TAX)化疗治疗皮质类固醇难治性前列腺癌(CRPC)的疗效尚不确定。

材料与方法

我们回顾性分析了在我院治疗的 51 例皮质类固醇难治性 CRPC 患者的结局。其中,24 例患者在 TAX 获得批准前仅接受地塞米松(DEX)治疗(历史对照)。其余 27 例患者在 TAX 获得批准后已经对 DEX 产生耐药性,接受了 TAX 加 DEX 治疗。

结果

接受 TAX 加 DEX 治疗的患者的中位总生存期(17.6 个月)明显长于仅接受 DEX 治疗的患者(8.1 个月,P = 0.021)。单因素分析显示,体能状态、乳酸脱氢酶(LDH)、碱性磷酸酶(ALP)、前列腺特异性抗原(PSA)和 TAX 治疗是总生存期的显著因素。其中,体能状态和 TAX 治疗在多因素分析中仍然是显著因素。对于晚期疾病患者,如体能状态较差、LDH 升高、ALP 升高或 PSA 升高,并未发现明显获益。TAX 治疗组出现 3、4 级毒性反应,包括贫血(19%)、白细胞减少(26%)和中性粒细胞减少(26%)。

结论

我们的结果表明,TAX 可能是 DEX 耐药性 CRPC 的重要选择,对于进展程度较低的患者可能更有效。

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