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在胶质母细胞瘤中,阳性 II 期临床试验的研究治疗方法无法随后预测阳性 III 期临床试验。

Inability of positive phase II clinical trials of investigational treatments to subsequently predict positive phase III clinical trials in glioblastoma.

机构信息

Baylor College of Medicine, Department of Neurology, Houston, Texas, USA.

Rabin Medical Center, Department of Neurosurgery, Petah Tikva, Israel.

出版信息

Neuro Oncol. 2018 Jan 10;20(1):113-122. doi: 10.1093/neuonc/nox144.

Abstract

BACKGROUND

Glioblastoma is the most common primary malignant brain tumor in adults, but effective therapies are lacking. With the scarcity of positive phase III trials, which are increasing in cost, we examined the ability of positive phase II trials to predict statistically significant improvement in clinical outcomes of phase III trials.

METHODS

A PubMed search was conducted to identify phase III clinical trials performed in the past 25 years for patients with newly diagnosed or recurrent glioblastoma. Trials were excluded if they did not examine an investigational chemotherapy or agent, if they were stopped early owing to toxicity, if they lacked prior phase II studies, or if a prior phase II study was negative.

RESULTS

Seven phase III clinical trials in newly diagnosed glioblastoma and 4 phase III clinical trials in recurrent glioblastoma met the inclusion criteria. Only 1 (9%) phase III study documented an improvement in overall survival and changed the standard of care.

CONCLUSION

The high failure rate of phase III trials demonstrates the urgent need to increase the reliability of phase II trials of treatments for glioblastoma. Strategies such as the use of adaptive trial designs, Bayesian statistics, biomarkers, volumetric imaging, and mathematical modeling warrant testing. Additionally, it is critical to increase our expectations of phase II trials so that positive findings increase the probability that a phase III trial will be successful.

摘要

背景

胶质母细胞瘤是成人中最常见的原发性恶性脑肿瘤,但缺乏有效的治疗方法。随着成本不断增加的阳性 III 期临床试验越来越稀缺,我们研究了阳性 II 期临床试验在预测 III 期临床试验临床结果的统计学显著改善方面的能力。

方法

对过去 25 年来针对新诊断或复发性胶质母细胞瘤患者的 III 期临床试验进行了 PubMed 检索。如果试验未检查新的化疗药物或药物、因毒性而提前停止、缺乏 II 期研究或 II 期研究为阴性,则排除试验。

结果

符合纳入标准的新诊断胶质母细胞瘤的 7 项 III 期临床试验和复发性胶质母细胞瘤的 4 项 III 期临床试验。只有 1 项(9%)III 期研究记录了总生存期的改善,并改变了标准治疗方法。

结论

III 期试验的高失败率表明,迫切需要提高胶质母细胞瘤治疗的 II 期试验的可靠性。例如,使用适应性试验设计、贝叶斯统计学、生物标志物、体积成像和数学模型等策略值得测试。此外,提高我们对 II 期试验的期望至关重要,以便阳性结果增加 III 期试验成功的可能性。

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