Department of Solid Tumor Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Invest New Drugs. 2011 Dec;29(6):1441-8. doi: 10.1007/s10637-010-9428-0. Epub 2010 Apr 6.
Enzastaurin is an oral serine/threonine kinase inhibitor of the beta isoform of protein kinase C that may have therapeutic activity in prostate cancer. We explored the efficacy of enzastaurin on two cohorts of patients with prostate cancer progression in the castrate state.
A two-cohort phase II trial was conducted, with both groups participating simultaneously. Cohort 1 consisted of patients with non-metastatic castrate prostate-specific antigen progressive disease. Cohort 2 consisted of patients with castrate metastatic disease with progression following docetaxel-based chemotherapy. Patients in both cohorts received 500 mg/day enzastaurin.
Therapy was well tolerated in both cohorts. One complete response was observed in Cohort 1, with limited activity in the majority of patients. In Cohort 2, no objective responses were seen and the median progression-free survival (11 weeks [90% confidence interval: 7.6, 11.7]) did not differ from the historical control.
Enzastaurin as a single agent has limited activity in castrate progressive prostate cancer. Evaluation in combination with docetaxel is ongoing.
恩杂鲁胺是蛋白激酶 C 的β 同工型的丝氨酸/苏氨酸激酶抑制剂,可能在前列腺癌中有治疗活性。我们研究了恩杂鲁胺在去势状态下前列腺癌进展的两批患者中的疗效。
进行了一项两队列的二期试验,两组同时参与。队列 1 包括非转移性去势前列腺特异性抗原进展性疾病的患者。队列 2 包括接受多西他赛为基础化疗后发生转移且进展的去势转移性疾病患者。两组患者均接受 500 mg/天的恩杂鲁胺治疗。
两组患者的治疗均耐受良好。队列 1 观察到 1 例完全缓解,多数患者疗效有限。在队列 2 中,未观察到客观缓解,中位无进展生存期(11 周[90%置信区间:7.6,11.7])与历史对照无差异。
恩杂鲁胺作为单一药物在去势进展性前列腺癌中活性有限。正在评估与多西他赛联合应用的效果。