利用机器学习开发的预后模型的偏差风险:肿瘤学系统综述。

Paula Dhiman, Jie Ma, Constanza L Andaur Navarro, Benjamin Speich, Garrett Bullock, Johanna A A Damen, Lotty Hooft, Shona Kirtley, Richard D Riley, Ben Van Calster, Karel G M Moons, Gary S Collins
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引用次数: 0

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背景:预后模型在肿瘤学领域被广泛用于指导医疗决策。人们对利用机器学习开发的预后模型的偏倚风险及其在肿瘤学领域的临床应用障碍知之甚少:我们进行了一项系统性回顾,并在 MEDLINE 和 EMBASE 数据库中检索了 2019 年 1 月 1 日至 2019 年 9 月 5 日期间发表的使用机器学习方法开发预后模型的肿瘤学相关研究。主要结果是偏倚风险,使用预测模型偏倚风险评估工具(PROBAST)进行判断。我们通过开发分析和验证分析分别描述了总体偏倚风险和每个领域的偏倚风险:我们纳入了 62 篇出版物(48 篇仅开发;14 篇开发与验证)。所有出版物共开发了 152 个模型,37 个模型经过验证。84%(95% CI:77-89)的开发模型和 51%(95% CI:35-67)的验证模型总体上存在高偏倚风险。在模型开发和验证的总体偏倚风险判断中,分析中引入的偏倚是最大的因素。123个(81%,95% CI:73.8-86.4)已开发模型和19个(51%,95% CI:35.1-67.3)已验证模型因其分析而存在高偏倚风险,这主要是由于分析中的缺陷,包括样本量不足和分割样本内部验证:肿瘤学领域基于机器学习的预后模型质量较差,大多数模型存在较高的偏倚风险,不宜在临床实践中使用。亟需遵守更好的标准,重点关注样本量估算和分析方法,以提高这些模型的质量。
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Risk of bias of prognostic models developed using machine learning: a systematic review in oncology.

Background: Prognostic models are used widely in the oncology domain to guide medical decision-making. Little is known about the risk of bias of prognostic models developed using machine learning and the barriers to their clinical uptake in the oncology domain.

Methods: We conducted a systematic review and searched MEDLINE and EMBASE databases for oncology-related studies developing a prognostic model using machine learning methods published between 01/01/2019 and 05/09/2019. The primary outcome was risk of bias, judged using the Prediction model Risk Of Bias ASsessment Tool (PROBAST). We described risk of bias overall and for each domain, by development and validation analyses separately.

Results: We included 62 publications (48 development-only; 14 development with validation). 152 models were developed across all publications and 37 models were validated. 84% (95% CI: 77 to 89) of developed models and 51% (95% CI: 35 to 67) of validated models were at overall high risk of bias. Bias introduced in the analysis was the largest contributor to the overall risk of bias judgement for model development and validation. 123 (81%, 95% CI: 73.8 to 86.4) developed models and 19 (51%, 95% CI: 35.1 to 67.3) validated models were at high risk of bias due to their analysis, mostly due to shortcomings in the analysis including insufficient sample size and split-sample internal validation.

Conclusions: The quality of machine learning based prognostic models in the oncology domain is poor and most models have a high risk of bias, contraindicating their use in clinical practice. Adherence to better standards is urgently needed, with a focus on sample size estimation and analysis methods, to improve the quality of these models.

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