USING EVENTS FROM DROPOUTS IN NONPARAMETRIC SURVIVAL FUNCTION ESTIMATION WITH APPLICATION TO INCUBATION OF AIDS

被引:11
作者
HOOVER, DR
MUNOZ, A
CAREY, V
TAYLOR, JMG
VANRADEN, M
CHMIEL, JS
KINGSLEY, L
BACELLAR, H
JACOBSON, LP
KUO, V
PARK, L
SAAH, A
FARZADEGAN, H
GRAHAM, N
MARGOLICK, J
MCARTHUR, J
ODAKA, N
PHAIR, JP
COHEN, B
RINALDO, CR
ARMSTRONG, J
GUPTA, P
HO, M
DETELS, R
VISSCHER, BR
DUDLEY, J
FAHEY, JL
GIORGI, JV
IMAGAWA, D
VERMUND, SH
SCHRAGER, LK
KASLOW, RA
机构
[1] JOHNS HOPKINS SCH PUBL HLTH, DEPT EPIDEMIOL, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS SCH PUBL HLTH, DEPT BIOSTAT, BALTIMORE, MD 21205 USA
[3] NCI, BETHESDA, MD 20892 USA
[4] UNIV CALIF LOS ANGELES, SCH PUBL HLTH, DEPT BIOSTAT, LOS ANGELES, CA 90024 USA
[5] UNIV CALIF LOS ANGELES, JONSSON COMPREHENS CANC CTR, LOS ANGELES, CA 90024 USA
[6] NIAID, EPIDEMIOL & BIOMETRY BRANCH, BETHESDA, MD 20892 USA
[7] NORTHWESTERN UNIV, SCH MED, CTR CANC, KRISTALLOG SECT, CHICAGO, IL 60611 USA
[8] NORTHWESTERN UNIV, SCH MED, HOWARD BROWN MEM CLIN, CHICAGO, IL 60611 USA
[9] UNIV CALIF LOS ANGELES, SCH PUBL HLTH, LOS ANGELES, CA 90024 USA
[10] UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA 90024 USA
[11] UNIV PITTSBURGH, GRAD SCH PUBL HLTH, DEPT INFECT DIS & IMMUNOL, PITTSBURGH, PA 15261 USA
关键词
CENSORING METHOD; DROPOUT; INTERVAL CENSORING; NONPARAMETRIC SURVIVAL ANALYSIS; POSTDROPOUT RESPONSE; TRUNCATION;
D O I
10.2307/2290689
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Often postdropout responses (PDR) in study dropouts are identified from death/disease registries or other medical records. If all dropout is random, then use of postdropout responses while censoring other subjects at date of dropout (CDO/PDR) will bias non-parametric survival probability estimates downward. Censoring all individuals at the last date of study contact, ignoring postdropout information (CDO) will produce unbiased nonparametric survival estimates. As onset of the response sometimes incapacitates the individual, preventing further study participation, dropout is often positively correlated with response. In this case CDO/PDR tends to prevent nonparametric survival overestimation but could lead to underestimation. When all of the responses in dropouts are identified, then regardless of dropout cause, use of all postdropout information, together with censoring all other subjects at time of analysis (CTA/PDR) will produce unbiased minimum variance estimates. We analyze the bias properties of nonparametric survival estimates produced using CDO/PDR, CDO, and CTA/PDR censoring mechanisms under various causes of study dropout and degrees of postdropout response recovery. The goal is to identify which of these censoring methods best incorporates postdropout information. Postdropout information may create interval-censored data. To facilitate statistical analysis of such data, the likelihood function is formulated in terms of the hazard. This results in computationally simple nonparametric estimates and covariances for interval-censored and left-truncated data. An application to estimation of acquired immune deficiency (AIDS)-free time after human immunodeficiency virus (HIV)-I seroconversion using data from a long-term cohort study with considerable dropout is presented. Upper and lower bound estimates for AIDS-free survival probabilities derived using CDO and CDO/PDR are shown to be quite close when compared to the underlying variance of these estimates.
引用
收藏
页码:37 / 43
页数:7
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