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Precision medicine needs randomized clinical trials.精准医学需要随机临床试验。
Nat Rev Clin Oncol. 2017 May;14(5):317-323. doi: 10.1038/nrclinonc.2017.8. Epub 2017 Feb 7.
2
Quality of Life, Overall Survival, and Costs of Cancer Drugs Approved Based on Surrogate Endpoints.基于替代终点获批的癌症药物的生活质量、总生存期及成本
JAMA Intern Med. 2017 Feb 1;177(2):276-277. doi: 10.1001/jamainternmed.2016.7761.
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Current Incentives for Scientists Lead to Underpowered Studies with Erroneous Conclusions.当前对科学家的激励措施导致研究力度不足且结论错误。
PLoS Biol. 2016 Nov 10;14(11):e2000995. doi: 10.1371/journal.pbio.2000995. eCollection 2016 Nov.
4
Impact of IDH1 mutation status on outcome in clinical trials for recurrent glioblastoma.异柠檬酸脱氢酶1(IDH1)突变状态对复发性胶质母细胞瘤临床试验结果的影响。
J Neurooncol. 2016 Aug;129(1):147-54. doi: 10.1007/s11060-016-2157-2. Epub 2016 Jun 7.
5
The cost-effectiveness of tumor-treating fields therapy in patients with newly diagnosed glioblastoma.肿瘤电场治疗在新诊断胶质母细胞瘤患者中的成本效益
Neuro Oncol. 2016 Aug;18(8):1129-36. doi: 10.1093/neuonc/now102. Epub 2016 May 13.
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The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.2016 年世界卫生组织中枢神经系统肿瘤分类:概述。
Acta Neuropathol. 2016 Jun;131(6):803-20. doi: 10.1007/s00401-016-1545-1. Epub 2016 May 9.
7
Maintenance Therapy With Tumor-Treating Fields Plus Temozolomide vs Temozolomide Alone for Glioblastoma: A Randomized Clinical Trial.替莫唑胺联合肿瘤电场治疗与替莫唑胺单药治疗胶质母细胞瘤的维持治疗:一项随机临床试验。
JAMA. 2015 Dec 15;314(23):2535-43. doi: 10.1001/jama.2015.16669.
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The influence of industry sponsorship on the reporting of subgroup analyses within phase III randomised controlled trials in gastrointestinal oncology.产业资助对胃肠道肿瘤学 III 期随机对照试验亚组分析报告的影响。
Eur J Cancer. 2015 Dec;51(18):2732-9. doi: 10.1016/j.ejca.2015.08.030. Epub 2015 Nov 19.
9
Immunotherapy response assessment in neuro-oncology: a report of the RANO working group.神经肿瘤学中的免疫治疗反应评估:RANO工作组报告
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10
CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2008-2012.CBTRUS统计报告:2008 - 2012年美国原发性脑和中枢神经系统肿瘤诊断情况
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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.

DOI:10.1093/neuonc/nox144
PMID:29016865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5761583/
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。