scholarly journals Bayesian MLIRT-based joint models for multivariate longitudinal and survival data with multiple features

2021 ◽  
Vol 9 (1) ◽  
pp. 4
Author(s):  
Yangxin Huang ◽  
Jiaqing Chen ◽  
Lan Xu ◽  
Hanze Zhang ◽  
Yuanyuan Lu
Biometrics ◽  
2017 ◽  
Vol 74 (2) ◽  
pp. 685-693 ◽  
Author(s):  
Eleni-Rosalina Andrinopoulou ◽  
Paul H. C. Eilers ◽  
Johanna J. M. Takkenberg ◽  
Dimitris Rizopoulos

Entropy ◽  
2020 ◽  
Vol 23 (1) ◽  
pp. 50
Author(s):  
Valeria Leiva-Yamaguchi ◽  
Danilo Alvares

Joint models of longitudinal and survival outcomes have gained much popularity in recent years, both in applications and in methodological development. This type of modelling is usually characterised by two submodels, one longitudinal (e.g., mixed-effects model) and one survival (e.g., Cox model), which are connected by some common term. Naturally, sharing information makes the inferential process highly time-consuming. In particular, the Bayesian framework requires even more time for Markov chains to reach stationarity. Hence, in order to reduce the modelling complexity while maintaining the accuracy of the estimates, we propose a two-stage strategy that first fits the longitudinal submodel and then plug the shared information into the survival submodel. Unlike a standard two-stage approach, we apply a correction by incorporating an individual and multiplicative fixed-effect with informative prior into the survival submodel. Based on simulation studies and sensitivity analyses, we empirically compare our proposal with joint specification and standard two-stage approaches. The results show that our methodology is very promising, since it reduces the estimation bias compared to the other two-stage method and requires less processing time than the joint specification approach.


Author(s):  
D. O. Nyaboga ◽  
A. Mwangi ◽  
D. Lusweti

Missing data is a common problem in real word studies especially clinical studies. However, most people working with such data, often drop missing cases from individuals with incomplete observations that occur when patients do not complete the treatment or miss their scheduled visits. This may lead to misleading results and ultimately affect the decision of whether an intervention is good or bad for the patients under treatment. The comparison of Complete Case (CC) and Inverse Probability Weights (IPW) techniques of handling missing data in various models has been addressed, however little has been done to compare these methods when applied to joint models of longitudinal and time to event data. Therefore, this paper seeks to investigate the impact of assuming CC analysis on clinical data with missing cases, comparing it with IPW method when fitting joint models of longitudinal and survival data setting full data model as the baseline model. This paper made use of randomized aids clinical trial data. The model with Deviance Information Criteria (DIC) close to that of full data joint model is considered the best. From the results, joint models from full data, CC and IPW had DIC of 10603.94, 8410.33 and 10600.95 respectively. The joint model obtained from IPW data had a DIC too close to that of full data joint model as compared to model from CC data.


2010 ◽  
Vol 28 (16) ◽  
pp. 2796-2801 ◽  
Author(s):  
Joseph G. Ibrahim ◽  
Haitao Chu ◽  
Liddy M. Chen

Joint models for longitudinal and survival data are particularly relevant to many cancer clinical trials and observational studies in which longitudinal biomarkers (eg, circulating tumor cells, immune response to a vaccine, and quality-of-life measurements) may be highly associated with time to event, such as relapse-free survival or overall survival. In this article, we give an introductory overview on joint modeling and present a general discussion of a broad range of issues that arise in the design and analysis of clinical trials using joint models. To demonstrate our points throughout, we present an analysis from the Eastern Cooperative Oncology Group trial E1193, as well as examine some operating characteristics of joint models through simulation studies.


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