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Dolastatin-10 in metastatic melanoma: a phase II and pharmokinetic trial of the California Cancer Consortium.

机译:Dolastatin-10在转移性黑色素瘤中的应用:加利福尼亚癌症协会的II期临床研究和药物动力学研究。

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摘要

Dolastatin-10 is a novel pentapeptide agent originally isolated from the marine mollusk Dolabella auricularia with a mechanism of antitumor activity that involves the inhibition of microtubule assembly. We performed a Phase II trial of Dolastatin-10, 400 microg/m2 in patients with advanced melanoma who had received no prior chemotherapy. Dolastatin-10 pharmokinetics were evaluated in a subset of patients following courses 1 and 2. Twelve patients were treated with a median of 2 cycles of Dolastatin-10, and no patient experienced an objective response. The only grade >2 toxicities were grade 3 neutropenia uncomplicated by infection, occurring in 4 patients following the first treatment cycle. The total systemic clearance and volume of distribution at steady-state were 2.61 +/- 1.9 L/h/m2 and 28.4 +/- 13 L/m2, respectively. Due to prolonged terminal elimination. Dolastatin-10 plasma concentrations of greater than 1 nM were sustained for 24 h in all patients studied. Dolastatin-10 is unlikely to have substantial activity in the treatment of melanoma.
机译:Dolastatin-10是一种新颖的五肽药物,最初是从海洋软体动物小叶杜氏斑Do中分离出来的,具有抗肿瘤活性的机制,该机制涉及抑制微管组装。我们对未接受过化疗的晚期黑色素瘤患者进行了Dolastatin-10(400微克/平方米)的II期试验。在课程1和2之后,对一部分患者的Dolastatin-10药物动力学进行了评估。十二位患者接受了2个周期的Dolastatin-10周期中值治疗,没有患者出现客观反应。唯一的> 2级毒性反应是3例中性粒细胞减少症,没有感染引起,在第一个治疗周期后发生4例。稳态时的总全身清除率和分布体积分别为2.61 +/- 1.9 L / h / m2和28.4 +/- 13 L / m2。由于长期淘汰。在所有研究的患者中,持续超过24小时的Dolastatin-10血浆浓度均超过1 nM。 Dolastatin-10在黑色素瘤的治疗中不太可能具有实质活性。

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