Smith C J, Phillips A N, Youle M S, Sabin C A, Lampe F C, Tsintas R, Tyrer M, Johnson M A
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.
HIV Med. 2007 Jan;8(1):55-63. doi: 10.1111/j.1468-1293.2007.00431.x.
To describe outcomes in patients starting first-line antiretroviral regimens including lopinavir/ritonavir (LPV/r) in a routine clinic setting.
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.
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.
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.
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。
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。
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。
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。