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Nonlinear joint models for individual dynamic prediction of risk of death using Hamiltonian Monte Carlo: application to metastatic prostate cancer

机译:使用汉密尔顿蒙特卡洛法对死亡风险进行个体动态预测的非线性联合模型:在转移性前列腺癌中的应用

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Background Joint models of longitudinal and time-to-event data are increasingly used to perform individual dynamic prediction of a risk of event. However the difficulty to perform inference in nonlinear models and to calculate the distribution of individual parameters has long limited this approach to linear mixed-effect models for the longitudinal part. Here we use a Bayesian algorithm and a nonlinear joint model to calculate individual dynamic predictions. We apply this approach to predict the risk of death in metastatic castration-resistant prostate cancer (mCRPC) patients with frequent Prostate-Specific Antigen (PSA) measurements. Methods A joint model is built using a large population of 400 mCRPC patients where PSA kinetics is described by a biexponential function and the hazard function is a PSA-dependent function. Using Hamiltonian Monte Carlo algorithm implemented in Stan software and the estimated population parameters in this population as priors, the a posteriori distribution of the hazard function is computed for a new patient knowing his PSA measurements until a given landmark time. Time-dependent area under the ROC curve (AUC) and Brier score are derived to assess discrimination and calibration of the model predictions, first on 200 simulated patients and then on 196 real patients that are not included to build the model. Results Satisfying coverage probabilities of Monte Carlo prediction intervals are obtained for longitudinal and hazard functions. Individual dynamic predictions provide good predictive performances for landmark times larger than 12 months and horizon time of up to 18 months for both simulated and real data. Conclusions As nonlinear joint models can characterize the kinetics of biomarkers and their link with a time-to-event, this approach could be useful to improve patient’s follow-up and the early detection of most at risk patients.
机译:背景技术纵向和事件发生时间数据的联合模型越来越多地用于执行事件风险的单独动态预测。但是,在非线性模型中执行推理和计算单个参数的分布的困难将这种方法长期局限于纵向部分的线性混合效应模型。在这里,我们使用贝叶斯算法和非线性联合模型来计算单个动态预测。我们采用这种方法来预测经常进行前列腺特异性抗原(PSA)测量的转移性去势抵抗性前列腺癌(mCRPC)患者的死亡风险。方法使用大量400例mCRPC患者建立联合模型,其中PSA动力学由双指数函数描述,危险函数是PSA依赖性函数。使用在Stan软件中实现的汉密尔顿蒙特卡罗算法和该人口中的估计人口参数作为先验,可以计算出已知患者的PSA测量值直至给定界标时间为止的危险函数的后验分布。得出ROC曲线(AUC)和Brier评分下随时间变化的面积,以评估模型预测的区分和校准,首先对200位模拟患者进行治疗,然后对196位未包括在内的真实患者进行建模。结果获得了满足纵向和危险函数的蒙特卡洛预测区间的覆盖概率。单独的动态预测可为大于12个月的界标时间和高达18个月的模拟和真实数据的视界时间提供良好的预测性能。结论由于非线性关节模型可以表征生物标志物的动力学及其与事件发生时间的联系,因此这种方法可能有助于改善患者的随访和对大多数高危患者的早期发现。

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