Department of Cancer Studies and Molecular Medicine, University of Leicester, Leicester, United Kingdom.
J Thorac Oncol. 2012 Sep;7(9):1466-70. doi: 10.1097/JTO.0b013e318260dfb9.
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.
基于硼替佐米在间皮瘤中的有前景的临床前疗效,进行了一项单臂 II 期试验(爱尔兰合作肿瘤学研究组 05-10 研究),采用 Simon 的两阶段设计,以评估硼替佐米单药治疗一线(表现状态不佳)和二线环境中的疗效。Bcl-2 同源结构域 3 仅蛋白 Noxa 已被认为是硼替佐米诱导细胞凋亡的关键诱导剂。因此,在一项生物标志物研究子研究中,我们假设 Noxa 表达的缺乏可能与耐药性相关。在二线环境中,共招募了 23 名患者。接受四个周期硼替佐米治疗的一名患者(4.8%)确认部分缓解。一名患者病情稳定;然而,大多数患者在头两个周期内就出现了进展。中位无进展生存期和总生存期分别为 2.1 个月和 5.8 个月。在一线环境中,共入组了 10 名患者,没有观察到客观缓解的证据。在肿瘤分析中,所有活检均可见 Noxa 的表达。硼替佐米单药治疗在未选择的间皮瘤患者中没有足够的活性,不值得进一步研究。