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BIC/FTC/TAF单片方案真实世界临床疗效和安全性研究 被引量:1
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作者 滕芬 田波 +3 位作者 李重熙 金永梅 陈海云 刘俊 《昆明医科大学学报》 CAS 2024年第4期74-80,共7页
目的分析比克替拉韦/恩曲他滨/丙酚替诺福韦(bictegravir/emtricitabine/tenofovir alafenamide,BIC/FTC/TAF)三合一单片复方制剂在艾滋病抗病毒治疗患者中的疗效和安全性。方法纳入2022年2月1日至2022年6月1日期间接受单片复方制剂(BIC... 目的分析比克替拉韦/恩曲他滨/丙酚替诺福韦(bictegravir/emtricitabine/tenofovir alafenamide,BIC/FTC/TAF)三合一单片复方制剂在艾滋病抗病毒治疗患者中的疗效和安全性。方法纳入2022年2月1日至2022年6月1日期间接受单片复方制剂(BIC/FTC/TAF)的初治患者(初治组)和经历过治疗的患者(经治组),并使用前瞻性观察研究的方法对其治疗后的病毒学、免疫学和生化学指标进行了统计分析。结果基线共纳入了249名患者,其中经治组220例,初治组29例。48周时符合方案分析结果显示,初治组病毒完全抑制率为93.10%,经治组为98.55%。与基线相比,2组患者治疗48周后的CD4+T淋巴细胞计数和CD4^(+)/CD8^(+)T细胞比值均升高(P<0.001),血甘油三酯、总胆固醇、总胆红素和血肌酐较基线相比也有所升高,且差异具有统计学意义(P<0.05),门冬氨酸氨基转移酶和丙氨酸氨基转移酶较基线相比均有所降低,除了初治组丙氨酸氨基转移酶(P>0.05),其余3个差异均有统计学意义(P<0.05),而基于血肌酐估算的肾小球滤过率,初治组较基线有所改善(P<0.001),经治组无明显改变。结论BIC/FTC/TAF不论对初治患者还是经治患者均能有效抑制病毒的复制,提高患者的免疫能力,安全性也较好,是可以成为临床某些特定人群的首选治疗方案之一。 展开更多
关键词 HIV/AIDS bic/ftc/taf 真实世界 疗效 安全性
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BIC/FTC/TAF联合用药方案在不同HIV感染人群中的疗效和安全性研究
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作者 王燕 许景旭 +2 位作者 肖经纬 陈海龙 朱年青 《中国科技期刊数据库 医药》 2024年第12期239-245,共7页
系统评价一线抗病毒治疗方案BIC/FTC/TAF在不同HIV感染人群中的疗效和安全性。方法 检索知网和PubMed等数据库中BIC/FTC/TAF抗病毒治疗方案的随机对照试验并进行质量评价和数据提取,对HIV初治人群和经治人群接受比克替拉韦/恩曲他滨/富... 系统评价一线抗病毒治疗方案BIC/FTC/TAF在不同HIV感染人群中的疗效和安全性。方法 检索知网和PubMed等数据库中BIC/FTC/TAF抗病毒治疗方案的随机对照试验并进行质量评价和数据提取,对HIV初治人群和经治人群接受比克替拉韦/恩曲他滨/富马酸丙酚替诺福韦(BIC/FTC/TAF,必妥维?) 联合抗病毒治疗进行亚组分析,采用R ”metafor” 软件分析各亚组治疗失败风险和不良反应风险差异。结果 共纳入9篇随机临床试验文献,包含1648 名HIV初治患者和2856名HIV经治患者。Meta分析结果显示,初治人群接受BIC/FTC/TAF三联给药治疗48周后的抗病毒失败风险是对照组给药方案的0.82倍(OR=0.82,95%CI:0.61,1.09);经治HIV感染人群接受BIC/TAF/FTC三联方案治疗后发生病毒学失败的风险升高(OR=1.35,95%CI:0.96,1.90)。在安全性上,初治人群接受三联给药(BIC/FTC/TAF)治疗48周后发生不良反应的风险是基于多替拉韦(DTG)的治疗方案(DTG/3TC/ABC或DTG/3TC)的1.37倍(OR=1.37,95%CI:0.36,5.25),但是其严重不良反应风险并无显著差异(OR=1.06,95%CI:0.73,1.55)。经治人群接受BIC/TAF/FTC三联给药治疗48周后不良反应风险是低于对照组给药方案(OR=0.88,95%CI:0.49,1.59)。而严重不良反应发生率和对照组相比则无显著差异(OR=1.08,95%CI:0.79,1.47)。结论 相较于其他以整合酶抑制剂为核心的联合抗病毒治疗方案,BIC/FTC/TAF方案在经治人群中的抗病毒失败风险更低,BIC/FTC/TAF在初治人群中的安全性更高。 展开更多
关键词 比克替拉韦 bic/ftc/taf 整合酶抑制剂 病毒学失败 不良反应 荟萃分析
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Efficacy and safety of switching from lopinavir/ritonavir-based regimens to bictegravir/emtricitabine/tenofovir alafenamide in people living with HIV:A multicenter retrospective study
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作者 Jiantao Fu Yifan Guo +6 位作者 Guoxiang Zheng Zongxing Yang Jinchuan Shi Dingyan Yan Jianhua Yu Lijun Sun Hongxin Zhao 《Virologica Sinica》 2025年第5期835-841,共7页
In China,approximately 13% of people living with human immunodeficiency virus(HIV)(PLWH)are receiving lopinavir/ritonavir(LPV/r)-based regimens.These PLWH typically have a history of either treatment failure or intole... In China,approximately 13% of people living with human immunodeficiency virus(HIV)(PLWH)are receiving lopinavir/ritonavir(LPV/r)-based regimens.These PLWH typically have a history of either treatment failure or intolerance to first-line efavirenz-based regimens.Given the considerable pill burden and adverse effects associated with LPV/r,treatment optimization is important for this population.This multicenter retrospective study aimed to evaluate the efficacy and safety of switching from LPV/r-based regimens to the single-tablet regimen of bictegravir/emtricitabine/tenofovir alafenamide(BIC/FTC/TAF).Virological suppression rates(HIV-RNA<40 copies/mL)were primarily compared between the 48-week periods before and after switching to BIC/FTC/TAF.CD4 counts and metabolic data were also assessed.A total of 461 PLWH were recruited between January 2021 and December 2023,with 92.2% being male,a median age of 38 years,and a median antiretroviral therapy duration of 8 years.Prior to initiating LPV/r,23.0%(106/461)had documented virological failure.During LPV/r treatment,18.9%(20/106)of these individuals experienced viral rebound.Among all participants,the overall virological suppression rates significantly increased from 94.6%(pre-switch)to 98.6%(post-switch)(P<0.001).Notably,among participants with prior virological failure,suppression rates improved significantly from 81.1%to 97.2%(P<0.001),whereas no significant difference was observed in those without such history(from 98.6% to 99.2%,P=0.764).The median triglyceride level decreased from 2.4 mmol/L to 1.8 mmol/L(P<0.001),while no difference in CD4 counts was observed.These findings demonstrate that BIC/FTC/TAF is an effective and metabolically favorable treatment option for PLWH switching from LPV/r based regimens,regardless of whether they have a prior history of virological failure. 展开更多
关键词 Human immunodeficiency virus(HIV) Virological suppression LPV/r bic/ftc/taf Metabolic outcomes
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Changes in blood lipid levels and influencing factors among treatment-naïve adult male HlV/AlDS patients following BlC/FTC/TAF vs.3TC+EFV+TDF 被引量:3
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作者 Xi Wang An Liu +7 位作者 Zaicun Li Hongwei Zhang Ruojun Esther Wu Ying Shao Jianwei Li Jiangzhu Ye Wei Liu Lijun Sun 《Chinese Medical Journal》 SCIE CAS CSCD 2024年第12期1447-1452,共6页
Background:Antiretroviral therapy(ART)was often associated with dyslipidemia among human immunodeficiency virus(HIV)/acquired immunodeficiency syndrome(AIDS)patients.This study aimed to assess treatment-naïve adu... Background:Antiretroviral therapy(ART)was often associated with dyslipidemia among human immunodeficiency virus(HIV)/acquired immunodeficiency syndrome(AIDS)patients.This study aimed to assess treatment-naïve adult male patients with HIV/AIDS who initiated ART with either co-formulated bictegravir,emtricitabine,and tenofovir alafenamide(BIC/FTC/TAF)or lamivudine,efavirenz,and tenofovir disoproxil fumarate(3TC+EFV+TDF),monitoring at weeks 4,12,24,and 48.Methods:A case-control retrospective study was conducted.The newly diagnosed HIV-infected individuals attending the sexual transmission disease(STD)/AIDS clinic of Beijing Youan Hospital,Capital Medical University,from January to December 2021.The patients were divided into BIC/FTC/TAF group or 3TC+EFV+TDF group.High-density lipoprotein cholesterol(HDL-C),low-density lipoprotein cholesterol(LDL-C),triglyceride(TG),and total cholesterol(TC)at different time points over 48 weeks between two groups were compared.A multivariate Cox regression model was used to identify relevant influencing factors for the population at high risk of increased LDL-C.Results:A total of 870 participants,with 510 in BIC/FTC/TAF group and 360 in 3TC+EFV+TDF group.There were no statistically significant differences in median age,baseline CD4/CD8 ratio,median body mass index(BMI)between the two groups.In both two groups,levels of TG,TC,and LDL-C were higher at 4 weeks,12 weeks,and 24 weeks of treatment(all P<0.05),and there were no statistically significant differences at 48 weeks compared to those at baseline(all P>0.05).In addition,the differences in average changes of the level of TG,TC,HDL-C,and LDL-C from weeks 4,12,24,and 48 to baseline between two groups were not statistically significant(all P>0.05).Multivariate Cox proportional risk model analysis showed that initiating ART with HIV RNA≥10^(5)copies/mL(compared with<10^(5)copies/mL)was associated with an increased risk of elevated LDL-C(hazard ratio=1.26,95%confidence interval:1.07-1.48,P=0.005).Conclusions:Transient elevations in blood lipid levels(TC,TG,HDL-C,and LDL-C)were observed in treatment-naïve adult male HIV/AIDS patients with BIC/FTC/TAF at 4 weeks,12 weeks,and 24 weeks of treatment.However,these levels did not differ significantly from baseline after 48 weeks of treatment,regardless of whether patients were in the BIC/FTC/TAF or 3TC+EFV+TDF group. 展开更多
关键词 Antiretroviral therapy Blood lipids bictegravir/emtricitabine/tenofovir alafenamide Lamivudine efavirenz and tenofovir disoproxil fumarate bic/ftc/taf 3TC+EFV+TDF HIV AIDS
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艾考恩,丙替在成年获得性免疫缺陷综合征患者的临床应用 被引量:3
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作者 谭清 周仲辉 何盛华 《中国全科医学》 CAS 北大核心 2020年第23期2964-2968,共5页
随着抗逆转录病毒治疗的出现和广泛应用,获得性免疫缺陷综合征(AIDS)成为了一种慢性可控性疾病。目前AIDS仍不可治愈,患者仍需终生服药,但随着抗逆转录病毒药物不断更新,在保证抗病毒疗效的同时,选择服用方便、不良反应小、安全性和耐... 随着抗逆转录病毒治疗的出现和广泛应用,获得性免疫缺陷综合征(AIDS)成为了一种慢性可控性疾病。目前AIDS仍不可治愈,患者仍需终生服药,但随着抗逆转录病毒药物不断更新,在保证抗病毒疗效的同时,选择服用方便、不良反应小、安全性和耐受性好的药物对提高患者生存质量至关重要。艾考恩,丙替(Genvoya■),即艾维雷韦(EVG)、科比司他(COBI)、恩曲他滨(FTC)、替诺福韦艾拉酚胺(TAF),四药合一的复方单片制剂,简写为E/C/F/TAF,先后获得美国、欧盟以及中国食品药品监督管理局批准用于AIDS治疗。本文重点对Genvoya■的代谢作用机制、临床研究、药物相互作用及不良反应、耐药性相关的研究进行概述,以提高临床医师和患者对该药物的综合认识。 展开更多
关键词 获得性免疫缺陷综合征 抗逆转录病毒治疗 艾考恩 丙替 艾维雷韦 科比司他 恩曲他滨 替诺福韦艾拉酚胺
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Analysis of Service Utilization and Medication Adherence Among Attendees of HIV Nonoccupational Post-Exposure Prophylaxis Clinics—China,2022–2024
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作者 Mengnan Tan Jie Xu Wei Dong 《China CDC weekly》 2025年第34期1099-1105,共7页
Introduction:Human Immunodeficiency Virus(HIV)nonoccupational post-exposure prophylaxis(nPEP)clinics are specialized healthcare facilities that provide urgent medical interventions to individuals with potential high-r... Introduction:Human Immunodeficiency Virus(HIV)nonoccupational post-exposure prophylaxis(nPEP)clinics are specialized healthcare facilities that provide urgent medical interventions to individuals with potential high-risk HIV exposures.This study analyzed utilization patterns of HIV nPEP services in China and examined factors associated with medication adherence among consultees,providing evidence to inform further implementation and optimization of HIV nPEP interventions.Methods:We analyzed nPEP case data collected from the national nPEP data information system between November 1,2022,and November 1,2024,using SPSS 29.0 software.Chi-square tests were applied to analyze characteristics of nPEP consultees,and logistic regression models were used to identify factors influencing medication adherence and followup compliance among those who initiated treatment.Results:As of November 1,2024,924 nPEP clinics nationwide received 54,108 consultees,with 53,405(98.70%)initiating medication.Most individuals seeking services were male(88.63%),classified as high-risk(83.11%),and heterosexual with multiple partners(67.66%).The“BIC/FTC/TAF”regimen was selected by 63.07%of recipients.Nearly all users(99.03%)completed medication evaluation within 72 hours post-exposure.Among medication users,60.34%(30,650)adhered to the full 28-day regimen,and 60.10%(30,509)completed either onemonth or three-month follow-ups.Multivariate logistic regression analysis identified gender,exposure risk assessment results,exposure population classification,individual preferences,and medication regimen as significant factors influencing both 28-day medication adherence and follow-up compliance(P<0.05).Conclusions:nPEP clinic consultees in China are predominantly young male heterosexual individuals with multiple sexual partners,with most selecting the Biktarvy regimen.However,both current 28-day medication adherence and follow-up compliance rates remain suboptimal.High-risk men and those receiving the Biktarvy regimen demonstrate superior medication adherence and follow-up compliance compared to other groups.Further research is needed to develop targeted interventions to improve medication adherence and follow-up rates among nPEP recipients.Enhancing adherence and follow-up should be prioritized in future interventions,supported by continuous monitoring to inform timely intervention strategy adjustments. 展开更多
关键词 HIV Nonoccupational post exposure prophylaxis Medication adherence factors associated medication adherence Follow up compliance China bic ftc taf regimen Service utilization
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洛匹那韦/利托那韦联合恩曲他滨/丙酚替诺福韦方案用于新型冠状病毒肺炎治疗的临床研究方案(TARCoV研究) 被引量:2
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作者 江华 王宇 +5 位作者 王凯 杨兴详 张建成 邓洪飞 王璐 曾俊 《中华急诊医学杂志》 CAS CSCD 北大核心 2020年第3期346-349,共4页
目的探索以洛匹那韦/利托那韦(lopinave/litonawe,LPV/r)为骨干药物,联合恩曲他滨(emtricitabine,FTC)/丙酚替诺福韦(tenofovir alafenamide fumarate,TAF)FTC/TAF的联合抗病毒方案用于新型冠状病毒肺炎患者早期治疗的临床疗效。方法为... 目的探索以洛匹那韦/利托那韦(lopinave/litonawe,LPV/r)为骨干药物,联合恩曲他滨(emtricitabine,FTC)/丙酚替诺福韦(tenofovir alafenamide fumarate,TAF)FTC/TAF的联合抗病毒方案用于新型冠状病毒肺炎患者早期治疗的临床疗效。方法为真实世界临床研究,分为前瞻性干预队列(T1)和历史对照队列(T2)两组。T1组拟纳入确诊NCP的轻型和普通型患者90例,入组患者均为接受国家卫健委推荐的标准治疗方案,并均采用LPV/r+FTC/TAF联合用药。T2组为接受LPV/r抗病毒治疗的历史病例匹配组,共90例。比较两组患者生存率、病毒核酸转阴时间、发展成为ARDS率及住院时间等主要结局指标。结论本试验是一项真实世界临床研究,有望为临床工作者提供一种更加高效和快速的抗病毒疗法,本研究的实施还将进一步帮助其筛选有效治疗药物。 展开更多
关键词 新型冠状病毒肺炎 洛匹那韦/利托那韦(LPV/r) 恩曲他滨/丙酚替诺福韦(ftc/taf) 生存率 住院时间
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