Fillaux J, Delpierre C, Alvarez M, Jaafar A, Marchou B, Massip P, Cuzin L
Centre d'information et de soins sur l'immunodéficience humaine (CISIH), hôpital Purpan, place Baylac, 31059 Toulouse cedex, France.
Med Mal Infect. 2006 Jun;36(6):335-9. doi: 10.1016/j.medmal.2006.01.009. Epub 2006 May 2.
To determine predictive factors of treatment interruption (TI) duration within a cohort of HIV-1 infected patients having stopped their treatment with CD4 above 350 cells per mm(3).
Data were collected from computerized medical records. Patients were selected if they were HIV-1 positive, 18 years of age or older, and had stopped their treatment between January 1st, 1999 and July 1st, 2003, with CD4 count above 350 cells per mm(3). The study period was censored on October 1st, 2003. Patients were assessed every 3 months from inclusion to censure. A survival analysis using the Cox proportional hazard model was performed.
One hundred eighty-five patients were included. The median duration of TI was 43 weeks. Sixty-three patients remained off-treatment at censure. In the multivariate analysis, TI duration was shorter if CD4 nadir was below 250 cells per mm(3) before TI (relative hazard, 2.10), age superior to 40 (relative hazard, 1.72), viral load higher than 2.3 log.copies per ml (relative hazard, 1.52), and CDC class C (relative hazard, 1.78) at TI. Neither CD4 cell count at TI, numbers of treatments, nor duration of treatment and infection before TI were independent predictive factors of early treatment resumption (TR).
Some clinical and biological data may be used as predictive factors of early TR. Our results can have implications on future therapeutic strategies, in which the goal of therapy is to maintain CD4 cell count above a predetermined threshold using cycles of therapy followed by prolonged interruption according to CD4 count.
确定在CD4细胞计数高于每立方毫米350个细胞时停止治疗的人类免疫缺陷病毒1型(HIV-1)感染患者队列中治疗中断(TI)持续时间的预测因素。
从计算机化医疗记录中收集数据。入选患者为HIV-1阳性、年龄在18岁及以上,于1999年1月1日至2003年7月1日期间停止治疗,且CD4细胞计数高于每立方毫米350个细胞。研究期截至2003年10月1日。从纳入研究至 censure,每3个月对患者进行评估。采用Cox比例风险模型进行生存分析。
纳入185例患者。TI的中位持续时间为43周。63例患者在 censure时仍未接受治疗。在多变量分析中,如果TI前CD4最低点低于每立方毫米250个细胞(相对风险,2.10)、年龄大于40岁(相对风险,1.72)、病毒载量高于每毫升2.3 log拷贝(相对风险,1.52)以及TI时疾病控制中心(CDC)C类(相对风险,1.78),则TI持续时间较短。TI时的CD4细胞计数、治疗次数、TI前的治疗持续时间和感染持续时间均不是早期恢复治疗(TR)的独立预测因素。
一些临床和生物学数据可作为早期TR的预测因素。我们的结果可能对未来的治疗策略产生影响,在这些策略中,治疗目标是通过治疗周期维持CD4细胞计数高于预定阈值,然后根据CD4计数进行长时间中断治疗。