共 2 条
Estimation of conditional cumulative incidence functions under generalized semiparametric regression models with missing covariates, with application to analysis of biomarker correlates in vaccine trials
被引:0
|作者:
Sun, Yanqing
[1
]
Heng, Fei
[2
]
Lee, Unkyung
[3
]
Gilbert, Peter B.
[4
,5
]
机构:
[1] Univ N Carolina, Dept Math & Stat, Charlotte, NC 28223 USA
[2] Univ North Florida, Dept Math & Stat, Jacksonville, FL 32224 USA
[3] CBER, Food & Drug Adm, Silver Spring, MD 20993 USA
[4] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[5] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
来源:
基金:
美国国家科学基金会;
关键词:
Augmented inverse probability weighted complete-case estimation;
competing risks;
cumulative incidence function;
two-phase sampling;
vaccine-induced antibody immune response biomarkers;
PROPORTIONAL HAZARDS MODELS;
EFFICACY;
AIDSVAX;
COEFFICIENTS;
COHORT;
ALVAC;
D O I:
10.1002/cjs.11693
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:
This article presents generalized semiparametric regression models for conditional cumulative incidence functions with competing risks data when covariates are missing by sampling design or happenstance. A doubly robust augmented inverse probability weighted (AIPW) complete-case approach to estimation and inference is investigated. This approach modifies IPW complete-case estimating equations by exploiting the key features in the relationship between the missing covariates and the phase-one data to improve efficiency. An iterative numerical procedure is derived to solve the nonlinear estimating equations. The asymptotic properties of the proposed estimators are established. A simulation study examining the finite-sample performances of the proposed estimators shows that the AIPW estimators are more efficient than the IPW estimators. The developed method is applied to the RV144 HIV-1 vaccine efficacy trial to investigate vaccine-induced IgG binding antibodies to HIV-1 as correlates of acquisition of HIV-1 infection while taking account of whether the HIV-1 sequences are near or far from the HIV-1 sequences represented in the vaccine construct.
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页码:235 / 257
页数:23
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