Abstract
Original language | English |
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Pages (from-to) | 1166-1183 |
Number of pages | 18 |
Journal | Biometrical Journal |
Volume | 59 |
Issue number | 6 |
DOIs | |
Publication status | Published - 2017 |
Keywords
- Cure fraction
- Mixed models
- Repeated measures
- Spatial frailty
- Time-to-event analysis
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In: Biometrical Journal, Vol. 59, No. 6, 2017, p. 1166-1183.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Joint analysis of longitudinal and survival AIDS data with a spatial fraction of long-term survivors: A Bayesian approach
AU - Martins, R.
AU - Silva, G.L.
AU - Andreozzi, V.
N1 - Export Date: 11 December 2017 Correspondence Address: Martins, R.; Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Escola Superior de Saúde Egas Moniz, Quinta da Granja, Monte de CaparicaPortugal; email: ruimartins@egasmoniz.edu.pt References: Andrinopoulou, E.-R., Rizopoulos, D., Takkenberg, J., Lesaffre, E., Combined dynamic predictions using joint models of two longitudinal outcomes and competing risk data (2015) Statistical Methods in Medical Research, , https://doi.org/10.1177/0962280215588340; Banerjee, S., Carlin, B., Gelfand, A., (2004) Hierarchical Modeling and Analysis for Spatial Data, , Chapman & Hall/CRC, Boca Raton, FL; Berkson, J., Gage, R., Survival curve for cancer patients following treatment (1952) Journal of the American Statistical Association, 47, pp. 501-515; Besag, J., York, J., Mollie, A., Bayesian image restoration with two application in spatial statistics (1991) Annals of the Institute of Statistical Mathematics, 43, pp. 1-59; Brezger, A., Lang, S., Generalized structured additive regression based on Bayesian P-splines (2006) Computational Statistics and Data Analysis, 50, pp. 967-991; Brown, E.R., Ibrahim, J.G., Bayesian approaches to joint cure-rate and longitudinal models with applications to cancer vaccine trials (2003) Biometrics, 59, pp. 686-693; Brown, E.R., Ibrahim, J.G., DeGruttola, V., A flexible B-spline model for multiple longitudinal biomarkers and survival (2005) Biometrics, 61, pp. 64-73; Chen, M., Ibrahim, J., Sinha, D., A new Bayesian model for survival data with a surviving fraction (1999) Journal of the American Statistical Association, 94, pp. 909-919; Chen, M.H., Ibrahim, J.G., Sinha, D., A new joint model for longitudinal and survival data with a cure fraction (2004) Journal of Multivariate Analysis, 91, pp. 18-34; Christensen, R., Johnson, W., Branscum, A., Hanson, T., (2011) Bayesian Ideas and Data Analysis—An Introduction for Scientists and Statisticians, , CRC Press, Boca Raton, FL; Cooner, F., Banerjee, S., Carlin, B., Sinha, D., Flexible cure rate modeling under latent activation schemes (2007) Journal of the American Statistical Association, 102, pp. 560-572; Cooner, F., Banerjee, S., McBean, A.M., Modelling geographically referenced survival data with a cure fraction (2006) Statistical Methods in Medical Research, 15, pp. 307-324; Deapen, D., Cockburn, M., Pinder, R., Lu, S., Wohl, A., Population-based linkage of AIDS and cancer registries (2007) American Journal of Preventive Medicine, 33, pp. 134-136; Eilers, P., Marx, B., Flexible smoothing with B-splines and penalties (1996) Statistical Science, 11, pp. 89-102; Eilers, P., Marx, B., (2004) Splines, knots and penalties, , Technical report, Department of Medical Statistics, Leiden University Medical Center; Ewell, M., Ibrahim, J., The large sample distribution of the weighted log rank statistic under general local alternatives (1997) Lifetime Data Analysis, 3, pp. 5-12; Farewell, V., The use of mixture models for the analysis of survival data with long-term survivors (1982) Biometrics, 38, pp. 1041-1046; Farewell, V., Mixture models in survival analysis: are they worth the risk (1986) Canadian Journal of Statistics, 14, pp. 257-262; Faucett, C.L., Thomas, D.C., Simultaneously modelling censored survival data and repeatedly measured covariates: a Gibbs sampling approach (1996) Statistics in Medicine, 15, pp. 1663-1685; Fonseca, M., Lucena, F., Veloso, V., Carvalho, M., Accuracy of a probabilistic record linkage strategy applied to identify deaths among cases reported to the Brazilian AIDS surveillance database (2010) Cad. 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PY - 2017
Y1 - 2017
N2 - A typical survival analysis with time-dependent covariates usually does not take into account the possible random fluctuations or the contamination by measurement errors of the variables. Ignoring these sources of randomness may cause bias in the estimates of the model parameters. One possible way for overcoming that limitation is to consider a longitudinal model for the time-varying covariates jointly with a survival model for the time to the event of interest, thereby taking advantage of the complementary information flowing between these two-model outcomes. We employ here a Bayesian hierarchical approach to jointly model spatial-clustered survival data with a fraction of long-term survivors along with the repeated measurements of CD4+ T lymphocyte counts for a random sample of 500 HIV/AIDS individuals collected in all the 27 states of Brazil during the period 2002–2006. The proposed Bayesian joint model comprises two parts: on the one hand, a flexible model using Penalized Splines to better capture the nonlinear behavior of the different CD4 profiles over time; on the other hand, a spatial cure model to cope with the set of long-term survivor individuals. Our findings show that joint models considering this set of patients were the ones with the best performance comparatively to the more traditional survival approach. Moreover, the use of spatial frailties allowed us to map the heterogeneity in the disease risk among the Brazilian states. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
AB - A typical survival analysis with time-dependent covariates usually does not take into account the possible random fluctuations or the contamination by measurement errors of the variables. Ignoring these sources of randomness may cause bias in the estimates of the model parameters. One possible way for overcoming that limitation is to consider a longitudinal model for the time-varying covariates jointly with a survival model for the time to the event of interest, thereby taking advantage of the complementary information flowing between these two-model outcomes. We employ here a Bayesian hierarchical approach to jointly model spatial-clustered survival data with a fraction of long-term survivors along with the repeated measurements of CD4+ T lymphocyte counts for a random sample of 500 HIV/AIDS individuals collected in all the 27 states of Brazil during the period 2002–2006. The proposed Bayesian joint model comprises two parts: on the one hand, a flexible model using Penalized Splines to better capture the nonlinear behavior of the different CD4 profiles over time; on the other hand, a spatial cure model to cope with the set of long-term survivor individuals. Our findings show that joint models considering this set of patients were the ones with the best performance comparatively to the more traditional survival approach. Moreover, the use of spatial frailties allowed us to map the heterogeneity in the disease risk among the Brazilian states. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
KW - Cure fraction
KW - Mixed models
KW - Repeated measures
KW - Spatial frailty
KW - Time-to-event analysis
U2 - 10.1002/bimj.201600159
DO - 10.1002/bimj.201600159
M3 - Article
C2 - 28464317
SN - 0323-3847
VL - 59
SP - 1166
EP - 1183
JO - Biometrical Journal
JF - Biometrical Journal
IS - 6
ER -