Pour Sadaf Marashi, Woolley Ian, Canavan Peter, Chuah John, Russell Darren B, Law Matthew, Petoumenos Kathy
National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney, NSW 2052, Australia.
Sex Health. 2011 Sep;8(3):295-303. doi: 10.1071/SH10008.
Patients who have become triple class experienced (TCE) are at a high risk of exhausting available treatment options. This study aims to investigate factors associated with becoming TCE and to explore the effect of becoming TCE on survival. We also project the prevalence of TCE in Australia to 2012.
Patients were defined as TCE when they stopped a combination antiretroviral treatment (cART) that introduced the third of the three major antiretroviral classes. Cox proportional hazards models were used to investigate factors associated with TCE and the effect of TCE on survival. To project TCE prevalence, we used predicted rates of TCE by fitting a Poisson regression model, together with the estimated number of patients who started cART in each year in Australia, assuming a mortality rate of 1.5 per 100 person-years.
Of the 1498 eligible patients, 526 became TCE. Independent predictors of a higher risk of TCE included current CD4 counts below 200cellsμL(-1) and earlier calendar periods. No significant difference in survival was observed between those who were TCE and those who were not yet TCE. An increasing number of patients are using cART in Australia and if current trends continue, the number of patients who are TCE is estimated to increase from 2800 in 2003 to 5000 in 2012.
Our results suggest that the prevalence of TCE in Australia is estimated to plateau after 2003. However, as an increasing number of patients are becoming TCE, it is necessary to develop new drugs that come from new classes or do not have overlapping resistance.
已成为三重类别经验丰富(TCE)的患者面临可用治疗方案耗尽的高风险。本研究旨在调查与成为TCE相关的因素,并探讨成为TCE对生存的影响。我们还预测了到2012年澳大利亚TCE的患病率。
当患者停止引入三大抗逆转录病毒类别中第三种的联合抗逆转录病毒治疗(cART)时,被定义为TCE。采用Cox比例风险模型来研究与TCE相关的因素以及TCE对生存的影响。为了预测TCE患病率,我们通过拟合泊松回归模型来使用TCE的预测率,并结合澳大利亚每年开始cART的患者估计数量,假设死亡率为每100人年1.5例。
在1498名符合条件的患者中,526人成为TCE。TCE风险较高的独立预测因素包括当前CD4细胞计数低于200个/μL以及较早的日历时间段。TCE患者和非TCE患者之间在生存方面未观察到显著差异。在澳大利亚,越来越多的患者正在使用cART,如果当前趋势持续下去,预计TCE患者数量将从2003年的2800例增加到2012年的5000例。
我们的结果表明,澳大利亚TCE的患病率预计在2003年后趋于平稳。然而,由于越来越多的患者正成为TCE,有必要开发来自新类别或无交叉耐药性的新药。