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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >GDC-0449 in patients with advanced chondrosarcomas: A French sarcoma group/US and French national cancer institute single-arm phase ii collaborative study
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GDC-0449 in patients with advanced chondrosarcomas: A French sarcoma group/US and French national cancer institute single-arm phase ii collaborative study

机译:GDC-0449在晚期软骨肉瘤患者中的应用:法国肉瘤组织/美国和法国国家癌症研究所单臂ii期合作研究

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摘要

Background: Pre-clinical data have suggested a therapeutic role of Hedgehog (Hh) pathway inhibitors in chondrosarcoma. Methods: This phase II trial included patients with progressive advanced chondrosarcoma. They received GDC-0449 150 mg/day (days 1-28, 28-day cycle). The primary end point was the 6-month clinical benefit rate (CBR) defined as the proportion of patients with non-progressive disease at 6 months. A 6-month CBR of 40% was considered as a reasonable objective to claim drug efficacy. Results: Between February 2011 and February 2012, 45 patients were included. Twenty had received prior chemotherapy. Thirty-nine were assessable for efficacy. The 6-month CBR was 25.6% (95% confidence interval 13.0-42.1). All stable patients had grade 1 or 2 conventional chondrosarcoma with documented progression within the 6 months before inclusion. All but one with available data also had overexpression of the Hh ligand. Median progression-free and overall survivals were 3.5 and 12.4 months, respectively. The most frequent adverse events were grade 1 or 2 myalgia, dysgeusia and alopecia. Conclusions: GDC-0449 did not meet the primary end point of this trial. Results suggest some activity in a subset of patients with progressive grade 1 or 2 conventional chondrosarcoma. Further studies assessing its role in combination with chemotherapy are warranted.
机译:背景:临床前数据表明刺猬(Hh)途径抑制剂在软骨肉瘤中具有治疗作用。方法:II期临床试验包括进行性晚期软骨肉瘤患者。他们接受了150毫克/天的GDC-0449(1-28天,28天周期)。主要终点为6个月临床获益率(CBR),定义为6个月时非进展性疾病患者的比例。 40%的6个月CBR被认为是声称具有药物疗效的合理目标。结果:2011年2月至2012年2月,纳入45例患者。之前接受过二十次化疗。 39名患者可评估疗效。 6个月的CBR为25.6%(95%置信区间13.0-42.1)。所有稳定的患者均具有1级或2级常规软骨肉瘤,并在入组前6个月内有记录的进展。除了一个有可用数据的人,其他人都过表达Hh配体。中位无进展生存期和总生存期分别为3.5个月和12.4个月。最常见的不良事件是1或2级肌痛,消化不良和脱发。结论:GDC-0449没有达到该试验的主要终点。结果表明,在进行性1级或2级常规软骨肉瘤的一部分患者中有一定活动。评估其与化学疗法联合作用的进一步研究是必要的。

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