Mulato A S, Lamy P D, Miller M D, Li W X, Anton K E, Hellmann N S, Cherrington J M
Gilead Sciences, Inc., Foster City, California 94404, USA.
Antimicrob Agents Chemother. 1998 Jul;42(7):1620-8. doi: 10.1128/AAC.42.7.1620.
Adefovir dipivoxil [bis(pivaloyloxymethyl)-ester prodrug], an orally bioavailable prodrug of adefovir [9-(2-phosphonylmethoxyethyl)adenine], is currently in phase III clinical trials for the treatment of human immunodeficiency virus (HIV). In vitro experiments demonstrated that either a K65R or a K70E mutation in HIV reverse transcriptase (RT) was selected in the presence of adefovir, conferring a 16- or 9-fold decrease in susceptibility to adefovir, respectively. Previous data demonstrated that patients receiving adefovir dipivoxil monotherapy (125 mg daily) for 12 weeks experienced a median decrease in HIV RNA levels of 0.5 log10 copies/ml and that resistance to adefovir dipivoxil did not arise during that period. In the present investigation, a further study was undertaken to investigate whether RT mutations developed among viruses from patients who completed the 12-week study and who opted to enroll in a maintenance phase of prolonged (6- to 12-month) adefovir dipivoxil therapy (120 mg daily). Concomitant treatment with antiretroviral agents was permitted during the maintenance phase. The median decreases in HIV RNA levels for patients who completed 6 or 12 months of maintenance-phase dosing were 0.6 and 1.14 log10 copies/ml, respectively. The reductions in the HIV RNA levels were similar among patients who received adefovir dipivoxil with or without concomitant treatment with antiretroviral agents. Viruses from 8 of 29 patients dosed for up to 12 months developed RT mutations that were not present at baseline; these mutations may have been related to adefovir dipivoxil therapy. Viruses from two of the eight patients developed the K70E mutation while the patients were on therapy, but none of the viruses from patients developed the K65R RT substitution. Despite the development of RT mutations, sustained reductions (6 to 12 months) in viral load (> or = 0.7 log10 copies/ml decrease from baseline) were observed in all eight patients.
阿德福韦酯[双(新戊酰氧甲基)酯前体药物],即阿德福韦[9-(2-膦酰甲氧基乙基)腺嘌呤]的一种口服生物利用度前体药物,目前正处于治疗人类免疫缺陷病毒(HIV)的III期临床试验阶段。体外实验表明,在阿德福韦存在的情况下,HIV逆转录酶(RT)中会出现K65R或K70E突变,分别使对阿德福韦的敏感性降低16倍或9倍。先前的数据表明,接受阿德福韦酯单药治疗(每日125毫克)12周的患者,HIV RNA水平的中位数下降了0.5 log10拷贝/毫升,且在此期间未出现对阿德福韦酯的耐药性。在本研究中,进一步开展了一项研究,以调查在完成12周研究并选择进入延长(6至12个月)阿德福韦酯治疗(每日120毫克)维持阶段的患者的病毒中,是否会出现RT突变。维持阶段允许同时使用抗逆转录病毒药物进行治疗。完成6个月或12个月维持阶段给药的患者,HIV RNA水平的中位数下降分别为0.6和1.14 log10拷贝/毫升。接受阿德福韦酯治疗的患者,无论是否同时接受抗逆转录病毒药物治疗,其HIV RNA水平的降低情况相似。在接受长达12个月给药的29名患者中,有8名患者的病毒出现了基线时不存在的RT突变;这些突变可能与阿德福韦酯治疗有关。8名患者中有两名患者的病毒在治疗期间出现了K70E突变,但患者的病毒均未出现K65R RT替代。尽管出现了RT突变,但在所有8名患者中均观察到病毒载量持续降低(6至12个月)(从基线下降≥0.7 log10拷贝/毫升)。