A weighted logistic regression model for estimation of recurrence of adenomas

被引:9
作者
Hsu, Chiu-Hsieh
Green, Sylvan B.
He, Yulei
机构
[1] Univ Arizona, Mel & Enid Zuckerman Coll Publ Hlth, Div Epidemiol & Biostat, Tucson, AZ 85724 USA
[2] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[3] Harvard Univ, Sch Med, Dept Hlth Care Policy, Boston, MA 02118 USA
关键词
colon cancer; current status data; logistic regression; non-parametric maximum likelihood estimator; weight function;
D O I
10.1002/sim.2648
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
In a colorectal polyp prevention trial, some participants might have their follow-up colonoscopy conducted before the scheduled time (i.e. at the end of the trial). This results in variable follow-up lengths for participants and the data of recurrence status at the end of the trial can be considered as current status data. In this paper, we use a weighted logistic regression model to estimate recurrence rate of adenoma data at the end of the trial. The weights are used to adjust for variable follow-up. We show that logistic regression tends to underestimate recurrence rate. In a simulation study, we show that Kaplan-Meier estimator derived from the right endpoint of the current status data tends to overestimate recurrence rate in contrast to logistic regression and the weighted logistic regression method can produce reasonable estimates of recurrence rate even under a high non-compliance rate compared to conventional logistic regression and Kaplan-Meier estimator. The method described here is illustrated with an example from a colon cancer study. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1567 / 1578
页数:12
相关论文
共 13 条
[1]
Phase III trial of ursodeoxycholic acid to prevent colorectal adenoma recurrence [J].
Alberts, DS ;
Martínez, ME ;
Hess, LM ;
Einspahr, JG ;
Green, SB ;
Bhattacharyya, AK ;
Guillen, J ;
Krutzsch, M ;
Batta, AK ;
Salen, G ;
Fales, L ;
Koonce, K ;
Parish, D ;
Clouser, M ;
Roe, D ;
Lance, P .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (11) :846-853
[2]
Sequential designs for phase I clinical trials with late-onset toxicities [J].
Cheung, YK ;
Chappell, R .
BIOMETRICS, 2000, 56 (04) :1177-1182
[3]
MULTIPLE IMPUTATION FOR THRESHOLD-CROSSING DATA WITH INTERVAL CENSORING [J].
DOREY, FJ ;
LITTLE, RJA ;
SCHENKER, N .
STATISTICS IN MEDICINE, 1993, 12 (17) :1589-1603
[4]
Efron B, 1967, Proceedings of the 5th Berkeley Symposium on Mathematical Statistics and Probability, V4, P831
[5]
Einspahr JG, 1997, CANCER EPIDEM BIOMAR, V6, P37
[6]
GILL R. D., 1980, Censoring and Stochastic Integrals, V124
[7]
Joint modelling of recurrence and progression of adenomas: a latent variable approach [J].
Hsu, CH .
STATISTICAL MODELLING, 2005, 5 (03) :201-215
[8]
KLEIN JP, 1991, SCAND J STAT, V18, P333
[9]
EFFECTS OF MIDPOINT IMPUTATION ON THE ANALYSIS OF DOUBLY CENSORED-DATA [J].
LAW, CG ;
BROOKMEYER, R .
STATISTICS IN MEDICINE, 1992, 11 (12) :1569-1578
[10]
MAXIMUM-LIKELIHOOD-ESTIMATION FOR INTERVAL-CENSORED DATA USING A WEIBULL-BASED ACCELERATED FAILURE TIME MODEL [J].
ODELL, PM ;
ANDERSON, KM ;
DAGOSTINO, RB .
BIOMETRICS, 1992, 48 (03) :951-959