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Combination therapy of recurrent prostate cancer with the proteasome inhibitor bortezomib plus hormone blockade.

机译:蛋白酶体抑制剂硼替佐米加激素阻断剂联合治疗复发性前列腺癌。

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摘要

A single arm phase II trial of single-agent bortezomib (BZM) alone or combined with hormone blockade was conducted in patients with early PSA recurrence after definitive local therapy. The primary endpoint of this study was to determine the time to PSA relapse after BZM therapy alone or when BZM was combined with hormone blockade. The secondary endpoint was to determine the safety of combination therapy. Part A of the treatment schedule consisted of three cycles of BZM 1.3 mg/m2 IV given on days 1,4,8,11. If patients progressed on Part A, they were entered on Part B which consisted of a single dose of LH-RH antagonist, daily oral antiandrogen, and weekly BZM 1.3 mg/m2 for three out of four weeks for a total of three months. BZM treatment significantly decreased the slope of the log PSA (p=0.024) demonstrating that this agent alone was capable of slowing the rise of the PSA. Of eight patients treated with BZM alone five had stable disease, two progressed and 1 went off study secondary to toxicity. The major toxicity was neurotoxicity requiring discontinuation of therapy in three patients and treatment interruption in nine patients. Of those receiving Parts A and B or B only, there were 11 of 15 CRs with the average time to progression of 5.5 months. BZM treatment can change the slope of PSA rise and can be combined with hormone deprivation therapy without significant additional side effects; these agents are associated with a median time to CR of 42 days.
机译:在明确的局部治疗后,PSA早期复发的患者进行了单药硼替佐米(BZM)单独或联合激素阻断的单臂II期试验。这项研究的主要终点是确定仅BZM治疗后或BZM合并激素阻断后PSA复发的时间。次要终点是确定联合治疗的安全性。治疗方案的A部分由在第1,4,8,11天给予的三个周期的BZM 1.3 mg / m2 IV周期组成。如果患者进展为A部分,则进入B部分,其中包括单剂量的LH-RH拮抗剂,每日口服抗雄激素和每周BZM 1.3 mg / m2,共四周中的三周,共三个月。 BZM处理显着降低了对数PSA的斜率(p = 0.024),表明该试剂本身能够减缓PSA的升高。单独接受BZM治疗的8例患者中,有5例疾病稳定,2例进展,1例因毒性反应而退出研究。主要毒性反应是神经毒性,其中三名患者需要中断治疗,九名患者需要中断治疗。仅接受A,B或B部分的患者中,有15个CR中有11个CR,平均进展时间为5.5个月。 BZM治疗可以改变PSA升高的斜率,并且可以与激素剥夺疗法联合使用,而没有明显的其他副作用;这些药物与CR的中位时间为42天有关。

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