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唑来膦酸和多西他赛联合节拍式给药在去势抵抗性前列腺癌患者中的应用:I 期 ZANTE 试验。

Metronomic administration of zoledronic acid and taxotere combination in castration resistant prostate cancer patients: phase I ZANTE trial.

机构信息

Genito-Urinary Department, National Cancer Institute Fondazione G Pascale, Naples, Italy.

出版信息

Cancer Biol Ther. 2010 Sep 15;10(6):543-8. doi: 10.4161/cbt.10.6.12611. Epub 2010 Sep 8.

Abstract

BACKGROUND

Docetaxel (DTX) and zoledronic acid (ZOL) are effective in patients with hormone resistant prostate cancer (HRPC) with bone metastases. A phase I clinical trial of metronomic administration of Zoledronic Acid AN d TaxoterE combination (ZANTE trial) in 2 different sequences was conducted in HRPC.

RESULTS

The maximum tolerated dose was not achieved with sequence A. Two patients at third level of sequence B developed dose limiting toxicity. A disease control was obtained in six out of nine patients treated with sequence A, where a decrease of biological markers and PSA were also observed. No evidence of anti-tumor activity was observed in patients treated with sequence B.

PATIENTS AND METHODS

Twenty-two patients enrolled into the study (median age: 73 years; range: 43-80) received one of three escalated doses of DTX (30, 40 and 50 mg/m(2)) in combination with a fixed dose of ZOL (2 mg), both administered every 14 days in two different sequences: DTX at the day 1 followed by ZOL at the day 2 (sequence A) or the reverse (sequence B). Patients were evaluated for adverse events and serum IL-8, MMP-2 and MMP-9 were evaluated prior and after therapy with the two sequences of administration of DTX and ZOL.

CONCLUSIONS

The bi-weekly combination of DTX (50 mg/m(2)) followed by ZOL was feasible and show promising anti-tumor activity.

摘要

背景

多西紫杉醇(DTX)和唑来膦酸(ZOL)在有骨转移的激素难治性前列腺癌(HRPC)患者中有效。在 HRPC 中进行了一项关于唑来膦酸和 TaxoterE 联合(ZANTE 试验)按两种不同顺序进行的节拍式给药的 I 期临床试验。

结果

A 序未达到最大耐受剂量。B 序的第 3 级的 2 例患者出现剂量限制毒性。A 序治疗的 9 例患者中有 6 例获得疾病控制,同时观察到生物标志物和 PSA 下降。B 序治疗的患者无抗肿瘤活性证据。

患者和方法

22 例患者入组研究(中位年龄:73 岁;范围:43-80),以三种递增剂量的 DTX(30、40 和 50mg/m²)与固定剂量的 ZOL(2mg)联合使用,每 14 天在两种不同的顺序给药:第 1 天 DTX 随后第 2 天 ZOL(A 序)或相反(B 序)。评估患者的不良反应,并用两种 DTX 和 ZOL 给药顺序治疗前后评估血清 IL-8、MMP-2 和 MMP-9。

结论

每周两次的 DTX(50mg/m²)联合 ZOL 是可行的,且显示出有希望的抗肿瘤活性。

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