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预测多发性硬化症的残疾进展:先进统计建模的见解

Predicting disability progression in multiple sclerosis: Insights from advanced statistical modeling.

作者信息

Pellegrini Fabio, Copetti Massimiliano, Sormani Maria Pia, Bovis Francesca, de Moor Carl, Debray Thomas Pa, Kieseier Bernd C

机构信息

Biogen International GmbH, Zug, Switzerland.

Unit of Biostatistics, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.

出版信息

Mult Scler. 2020 Dec;26(14):1828-1836. doi: 10.1177/1352458519887343. Epub 2019 Nov 5.

Abstract

BACKGROUND

There is an unmet need for precise methods estimating disease prognosis in multiple sclerosis (MS).

OBJECTIVE

Using advanced statistical modeling, we assessed the prognostic value of various clinical measures for disability progression.

METHODS

Advanced models to assess baseline prognostic factors for disability progression over 2 years were applied to a pooled sample of patients from placebo arms in four different phase III clinical trials. least absolute shrinkage and selection operator (LASSO) and ridge regression, elastic nets, support vector machines, and unconditional and conditional random forests were applied to model time to clinical disability progression confirmed at 24 weeks. Sensitivity analyses for different definitions of a combined endpoint were carried out, and bootstrap was used to assess prediction model performance.

RESULTS

A total of 1582 patients were included, of which 434 (27.4%) had disability progression in a combined endpoint over 2 years. Overall model discrimination performance was relatively poor (all -indices ⩽ 0.65) across all models and across different definitions of progression.

CONCLUSION

Inconsistency of prognostic factor importance ranking confirmed the relatively poor prediction ability of baseline factors in modeling disease progression in MS. Our findings underline the importance to explore alternative predictors as well as alternative definitions of commonly used endpoints.

摘要

背景

对于精确估计多发性硬化症(MS)疾病预后的方法仍存在未满足的需求。

目的

使用先进的统计模型,我们评估了各种临床指标对残疾进展的预后价值。

方法

将用于评估2年期间残疾进展基线预后因素的先进模型应用于来自四项不同III期临床试验安慰剂组患者的汇总样本。应用最小绝对收缩和选择算子(LASSO)、岭回归、弹性网络、支持向量机以及无条件和条件随机森林来对24周时确认的临床残疾进展时间进行建模。对联合终点的不同定义进行了敏感性分析,并使用自助法评估预测模型的性能。

结果

共纳入1582例患者,其中434例(27.4%)在2年的联合终点中有残疾进展。在所有模型以及不同进展定义中,总体模型区分性能相对较差(所有指标⩽0.65)。

结论

预后因素重要性排名的不一致证实了基线因素在MS疾病进展建模中的预测能力相对较差。我们的研究结果强调了探索替代预测指标以及常用终点的替代定义的重要性。

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