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在皇家自由医院,开始接受含洛匹那韦/利托那韦抗逆转录病毒治疗方案的既往未接受过抗逆转录病毒治疗的HIV感染患者的治疗结果。

Treatment outcomes amongst previously antiretroviral-naïve HIV-infected patients starting lopinavir/ritonavir-containing antiretroviral regimens at the Royal Free Hospital.

作者信息

Smith C J, Phillips A N, Youle M S, Sabin C A, Lampe F C, Tsintas R, Tyrer M, Johnson M A

机构信息

Royal Free Centre for HIV Medicine and Department of Primary Care and Population Sciences, Royal Free and University College Medical School, Rowland Hill Street, London, UK.

出版信息

HIV Med. 2007 Jan;8(1):55-63. doi: 10.1111/j.1468-1293.2007.00431.x.

Abstract

OBJECTIVE

To describe outcomes in patients starting first-line antiretroviral regimens including lopinavir/ritonavir (LPV/r) in a routine clinic setting.

METHODS

Previously naïve patients starting LPV/r-containing antiretroviral therapy were included in the study. Virological failure was defined as the first of two viral loads >500 HIV-1 RNA copies/mL more than 6 months after starting LPV/r. Cumulative percentages experiencing virological failure were calculated using Kaplan-Meier methods.

RESULTS

A total of 195 individuals had a median follow-up time of 1.7 years. At 48 weeks, 87.9, 77.4 and 71.6% of patients with pretreatment CD4 counts of <50, 50-200 and >200 cells/microL, respectively, remained on LPV/r. By 48, 72 and 96 weeks, 2.2, 3.0 and 5.0% of patients, respectively, had experienced virological failure, ignoring treatment changes but censoring follow-up at discontinuation of all antiretrovirals; these percentages became 24.0, 33.7 and 42.3% when LPV/r discontinuation was considered as virological failure. Censoring those who stopped LPV/r with a viral load <50 copies/mL and considering as virological failures those who stopped LPV/r with a viral load >50 copies/mL gave 12.1, 14.6 and 17.0% virological failure at 48, 72 and 96 weeks, respectively. Median CD4 count increases at 24, 48 and 72 weeks were 167, 230 and 253 cells/microL, respectively.

CONCLUSIONS

Few patients experienced virological failure whilst on a LPV/r-based regimen, although it was not uncommon for patients in our clinic with higher baseline CD4 counts to discontinue LPV/r.

摘要

目的

描述在常规门诊环境中开始使用包括洛匹那韦/利托那韦(LPV/r)在内的一线抗逆转录病毒治疗方案的患者的治疗结果。

方法

本研究纳入了之前未接受过治疗且开始含LPV/r的抗逆转录病毒治疗的患者。病毒学失败定义为在开始使用LPV/r超过6个月后,首次出现两次病毒载量>500 HIV-1 RNA拷贝/mL。使用Kaplan-Meier方法计算发生病毒学失败的累积百分比。

结果

共有195例患者,中位随访时间为1.7年。在48周时,治疗前CD4细胞计数分别<50、50 - 200和>200个细胞/微升的患者中,分别有87.9%、77.4%和71.6%仍在使用LPV/r。到48、72和96周时,分别有2.2%、3.0%和5.0%的患者出现病毒学失败,忽略治疗方案的改变,但在所有抗逆转录病毒药物停药时终止随访;当将LPV/r停药视为病毒学失败时,这些百分比分别变为24.0%、33.7%和42.3%。对病毒载量<50拷贝/mL时停用LPV/r的患者进行截尾,将病毒载量>50拷贝/mL时停用LPV/r的患者视为病毒学失败,在48、72和96周时病毒学失败率分别为12.1%、14.6%和17.0%。在24、48和72周时,CD4细胞计数的中位增加值分别为167、230和253个细胞/微升。

结论

在基于LPV/r的治疗方案中,很少有患者出现病毒学失败,尽管在我们诊所中基线CD4细胞计数较高的患者停用LPV/r的情况并不少见。

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