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1
Predicting analysis times in randomized clinical trials with cancer immunotherapy.癌症免疫疗法随机临床试验中的分析时间预测分析
BMC Med Res Methodol. 2016 Feb 1;16:12. doi: 10.1186/s12874-016-0117-3.
2
Real-time prediction of clinical trial enrollment and event counts: A review.临床试验入组和事件计数的实时预测:综述
Contemp Clin Trials. 2015 Nov;45(Pt A):26-33. doi: 10.1016/j.cct.2015.07.010. Epub 2015 Jul 16.
3
Bayesian modeling and prediction of accrual in multi-regional clinical trials.多区域临床试验中应计项目的贝叶斯建模与预测
Stat Methods Med Res. 2017 Apr;26(2):752-765. doi: 10.1177/0962280214557581. Epub 2014 Nov 3.
4
Management of oropharyngeal cancer: a cross-sectional review of institutional practice at a large Canadian referral centre.口咽癌的管理:对加拿大一家大型转诊中心机构实践的横断面回顾。
J Otolaryngol Head Neck Surg. 2014 Jun 24;43(1):19. doi: 10.1186/1916-0216-43-19.
5
Prediction of event times in the REMATCH Trial.REMATCH 试验中事件时间的预测。
Clin Trials. 2013 Apr;10(2):197-206. doi: 10.1177/1740774512470314. Epub 2013 Jan 15.
6
Cure models as a useful statistical tool for analyzing survival.治愈模型作为一种有用的统计工具,可用于分析生存情况。
Clin Cancer Res. 2012 Jul 15;18(14):3731-6. doi: 10.1158/1078-0432.CCR-11-2859. Epub 2012 Jun 6.
7
Modeling and prediction of subject accrual and event times in clinical trials: a systematic review.临床试验中受试者入组和事件时间的建模与预测:系统评价。
Clin Trials. 2012 Dec;9(6):681-8. doi: 10.1177/1740774512447996. Epub 2012 Jun 6.
8
Prediction of accrual closure date in multi-center clinical trials with discrete-time Poisson process models.使用离散时间泊松过程模型预测多中心临床试验中的入组截止日期。
Pharm Stat. 2012 Sep-Oct;11(5):351-6. doi: 10.1002/pst.1506. Epub 2012 Mar 12.
9
A hybrid approach to predicting events in clinical trials with time-to-event outcomes.一种混合方法,用于预测具有时间事件结局的临床试验中的事件。
Contemp Clin Trials. 2011 Sep;32(5):755-9. doi: 10.1016/j.cct.2011.05.013. Epub 2011 May 30.
10
Human papillomavirus and survival of patients with oropharyngeal cancer.人乳头瘤病毒与口咽癌患者的生存。
N Engl J Med. 2010 Jul 1;363(1):24-35. doi: 10.1056/NEJMoa0912217. Epub 2010 Jun 7.

实时预测中的治愈建模:它有多大帮助?

Cure modeling in real-time prediction: How much does it help?

作者信息

Ying Gui-Shuang, Zhang Qiang, Lan Yu, Li Yimei, Heitjan Daniel F

机构信息

Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Biostatistics & Epidemiology, University of Pennsylvania, Philadelphia, PA 19104, USA.

NRG Oncology Statistics & Data Management Center, Philadelphia, PA 19103, USA.

出版信息

Contemp Clin Trials. 2017 Aug;59:30-37. doi: 10.1016/j.cct.2017.05.012. Epub 2017 May 22.

DOI:10.1016/j.cct.2017.05.012
PMID:28545934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5571982/
Abstract

Various parametric and nonparametric modeling approaches exist for real-time prediction in time-to-event clinical trials. Recently, Chen (2016 BMC Biomedical Research Methodology 16) proposed a prediction method based on parametric cure-mixture modeling, intending to cover those situations where it appears that a non-negligible fraction of subjects is cured. In this article we apply a Weibull cure-mixture model to create predictions, demonstrating the approach in RTOG 0129, a randomized trial in head-and-neck cancer. We compare the ultimate realized data in RTOG 0129 to interim predictions from a Weibull cure-mixture model, a standard Weibull model without a cure component, and a nonparametric model based on the Bayesian bootstrap. The standard Weibull model predicted that events would occur earlier than the Weibull cure-mixture model, but the difference was unremarkable until late in the trial when evidence for a cure became clear. Nonparametric predictions often gave undefined predictions or infinite prediction intervals, particularly at early stages of the trial. Simulations suggest that cure modeling can yield better-calibrated prediction intervals when there is a cured component, or the appearance of a cured component, but at a substantial cost in the average width of the intervals.

摘要

在生存时间临床试验的实时预测中,存在各种参数和非参数建模方法。最近,Chen(2016年,《BMC生物医学研究方法》第16卷)提出了一种基于参数治愈混合模型的预测方法,旨在涵盖那些似乎有不可忽略比例的受试者被治愈的情况。在本文中,我们应用威布尔治愈混合模型进行预测,在头颈部癌的随机试验RTOG 0129中展示该方法。我们将RTOG 0129中的最终实际数据与威布尔治愈混合模型、无治愈成分的标准威布尔模型以及基于贝叶斯自助法的非参数模型的中期预测进行比较。标准威布尔模型预测事件发生时间比威布尔治愈混合模型更早,但直到试验后期治愈证据变得明显时,差异才显著。非参数预测常常给出未定义的预测或无限的预测区间,尤其是在试验早期。模拟表明,当存在治愈成分或出现治愈成分的迹象时,治愈建模可以产生校准更好的预测区间,但区间的平均宽度会大幅增加。