Hu Liangyuan, Hogan Joseph W, Mwangi Ann W, Siika Abraham
Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Brown University School of Public Health, Providence, Rhode Island 02912, USA.
Biometrics. 2018 Jun;74(2):703-713. doi: 10.1111/biom.12780. Epub 2017 Sep 28.
The timing of antiretroviral therapy (ART) initiation for HIV and tuberculosis (TB) co-infected patients needs to be considered carefully. CD4 cell count can be used to guide decision making about when to initiate ART. Evidence from recent randomized trials and observational studies generally supports early initiation but does not provide information about effects of initiation time on a continuous scale. In this article, we develop and apply a highly flexible structural proportional hazards model for characterizing the effect of treatment initiation time on a survival distribution. The model can be fitted using a weighted partial likelihood score function. Construction of both the score function and the weights must accommodate censoring of the treatment initiation time, the outcome, or both. The methods are applied to data on 4903 individuals with HIV/TB co-infection, derived from electronic health records in a large HIV care program in Kenya. We use a model formulation that flexibly captures the joint effects of ART initiation time and ART duration using natural cubic splines. The model is used to generate survival curves corresponding to specific treatment initiation times; and to identify optimal times for ART initiation for subgroups defined by CD4 count at time of TB diagnosis. Our findings potentially provide 'higher resolution' information about the relationship between ART timing and mortality, and about the differential effect of ART timing within CD4 subgroups.
对于合并感染艾滋病毒(HIV)和结核病(TB)的患者,抗逆转录病毒疗法(ART)启动的时机需要仔细考虑。CD4细胞计数可用于指导何时启动ART的决策。近期随机试验和观察性研究的证据总体上支持早期启动,但未提供关于启动时间在连续尺度上的影响的信息。在本文中,我们开发并应用了一种高度灵活的结构比例风险模型,用于描述治疗启动时间对生存分布的影响。该模型可使用加权偏似然得分函数进行拟合。得分函数和权重的构建都必须考虑治疗启动时间、结局或两者的删失情况。这些方法应用于来自肯尼亚一个大型HIV护理项目电子健康记录的4903名HIV/TB合并感染个体的数据。我们使用一种模型公式,通过自然三次样条灵活地捕捉ART启动时间和ART持续时间的联合效应。该模型用于生成对应于特定治疗启动时间的生存曲线;并确定根据结核病诊断时的CD4计数定义的亚组的ART最佳启动时间。我们的研究结果可能提供关于ART启动时间与死亡率之间关系以及CD4亚组内ART启动时间差异效应的“更高分辨率”信息。