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首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Phase II clinical trial of first or second-line treatment with bortezomib in patients with malignant pleural mesothelioma
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Phase II clinical trial of first or second-line treatment with bortezomib in patients with malignant pleural mesothelioma

机译:硼替佐米一线或二线治疗恶性胸膜间皮瘤患者的II期临床试验

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摘要

Based on promising preclinical efficacy of bortezomib in mesothelioma, a single-arm phase II trial (Ireland Cooperative Oncology Research Group 05-10 study), with Simon's two-stage design, was undertaken to assess efficacy of bortezomib monotherapy in the first-line (poor performance status) and second-line settings. The Bcl-2 homology domain 3-only protein Noxa has been implicated as a key inducer of apoptosis by bortezomib. Thus, in a biomarker research substudy, we hypothesized that deficiency in Noxa expression might correlate with resistance. In the second-line setting, 23 patients were enrolled. Partial response was confirmed in one patient (4.8%) who received four cycles of bortezomib. One patient had stable disease; however, progression occurred in the majority of patients within the first two cycles. Median progression-free survival and overall survival were 2.1 and 5.8 months, respectively. In the first-line setting, ten patients were accrued, and there was no evidence of objective response. In the tumor analysis, expression of Noxa was seen in all biopsies. Bortezomib monotherapy exhibits insufficient activity to warrant further investigation in unselected patients with mesothelioma.
机译:基于硼替佐米在间皮瘤中的有希望的临床前疗效,采用西蒙的两阶段设计进行了一项单臂II期临床试验(爱尔兰合作肿瘤研究小组研究05-10),以评估硼替佐米单线治疗的一线疗效(性能状况不佳)和二线设置。 Bcl-2同源结构域3仅蛋白质Noxa已被认为是硼替佐米引起细胞凋亡的关键诱导剂。因此,在一个生物标记研究子中,我们假设Noxa表达的缺乏可能与耐药性相关。在二线治疗中,有23名患者入组。在接受硼替佐米四个疗程的一名患者(4.8%)中确认了部分反应。 1例患者病情稳定;但是,大多数患者在前两个周期内进展。中位无进展生存期和总生存期分别为2.1和5.8个月。在一线治疗中,有10名患者入选,没有客观反应的证据。在肿瘤分析中,在所有活组织检查中均观察到Noxa的表达。硼替佐米单药治疗的活性不足,无法对未选择的间皮瘤患者进行进一步研究。

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