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加权Kaplan-Meier估计量用于估计受检测限 censored的HIV-1 RNA减少情况。(注:这里“censored”在医学统计语境中通常指删失,因未达到检测限等原因部分数据无法准确记录完整,翻译中保留英文更准确传达专业含义,待根据具体专业知识进一步明确其准确翻译。)

Weighted Kaplan-Meier estimators motivating to estimate HIV-1 RNA reduction censored by a limit of detection.

作者信息

Ahmed Ismaïl, Flandre Philippe

机构信息

INSERM, Biostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases (B2PHI), UVSQ, Villejuif, France.

INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (IPLESP), Sorbonne Université, Paris, France.

出版信息

Stat Med. 2020 Mar 30;39(7):968-983. doi: 10.1002/sim.8455. Epub 2020 Jan 24.

Abstract

Measuring the magnitude of reduction in HIV-1 RNA levels accurately is difficult because many patients have a censored reduction due to the limit of detection (LOD) of the virologic assay being employed. The use of censored methods has improved the analysis of such reductions compared with crude methods but implies independent censoring. For HIV-1 RNA reduction data, the value at which a patient's HIV-1 RNA reduction becomes censored is mainly determined by the patient's baseline HIV-1 RNA level. We suggest two possibilities based on modification of the redistribution to the right algorithm to handle the situation of dependence either from a single continuous marker, that is, the baseline HIV-1 RNA level, or from multiple markers. Two series of simulation, one in the HIV-1 RNA setting and one in the classical censoring setting, compared performance of the previous methods with our suggestions. Our proposed estimators show good performances when the dependent censoring is due to LOD. Overall, in the classical censoring setting, our suggestions perform as well as other methods including the Inverse Probability of Censoring Weighted and the Kaplan-Meier imputation with Bootstrap. We applied those estimators to estimate the HIV-1 RNA reduction at week 8 of 502 patients who received a raltegravir-containing regimen and to data from the Mayo Clinic trial in primary biliary cirrhosis.

摘要

准确测量HIV-1 RNA水平的降低幅度很困难,因为许多患者由于所采用的病毒学检测方法的检测限(LOD)而出现删失性降低。与粗略方法相比,使用删失方法改善了对此类降低情况的分析,但意味着独立删失。对于HIV-1 RNA降低数据,患者的HIV-1 RNA降低变为删失值主要由患者的基线HIV-1 RNA水平决定。我们基于对向右重新分布算法的修改提出了两种可能性,以处理来自单个连续标志物(即基线HIV-1 RNA水平)或多个标志物的依赖情况。进行了两个系列的模拟,一个在HIV-1 RNA环境中,一个在经典删失环境中,将先前方法的性能与我们的建议进行了比较。当依赖删失是由于LOD时,我们提出的估计器表现良好。总体而言,在经典删失环境中,我们的建议与其他方法(包括删失加权逆概率法和带自助法的Kaplan-Meier插补法)表现相当。我们将这些估计器应用于估计502例接受含raltegravir方案治疗的患者在第8周时的HIV-1 RNA降低情况,并应用于梅奥诊所原发性胆汁性肝硬化试验的数据。

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