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Clopidogrel versus aspirin for coronary artery disease. 氯吡格雷与阿司匹林治疗冠状动脉疾病
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-28 DOI: 10.1016/S0140-6736(25)02644-3
Cinzia Dello Russo, Luigi Venetucci, Ronnie Ramlogan, Dimitri Gagliardi, Abisobe Akintola, Munir Pirmohamed
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引用次数: 0
Watching the watchers: a reply from Global Health Watch 7. 观察观察者:全球健康观察的回复。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-28 DOI: 10.1016/S0140-6736(26)00289-8
Ronald Labonté, Chiara Bodini
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引用次数: 0
Clopidogrel versus aspirin for coronary artery disease. 氯吡格雷与阿司匹林治疗冠状动脉疾病
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-28 DOI: 10.1016/S0140-6736(25)02645-5
Ahmed Ibrahim, Laila Shalabi, Giuseppe Andó
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引用次数: 0
Health and war in Sudan. 苏丹的健康和战争。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-26 DOI: 10.1016/S0140-6736(26)00415-0
Sharmila Devi
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引用次数: 0
Switch to single-tablet bictegravir-lenacapavir from a complex HIV regimen (ARTISTRY-1): a randomised, open-label, phase 3 clinical trial. 从复杂的HIV治疗方案(artiry -1)切换到单片双替格拉韦-lenacapavir:一项随机、开放标签的3期临床试验。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-25 DOI: 10.1016/S0140-6736(26)00307-7
Chloe Orkin, Peter J Ruane, Malcolm Hedgcock, Cyril Gaultier, Marcelo H Losso, Benoit Trottier, Thomas Lutz, Mark O'Reilly, Mark Bloch, Jihad Slim, Moti Ramgopal, Simiso Sokhela, Karam Mounzer, Hung-Chin Tsai, Jorge Santana Bagur, Xu Zhang, Keith Aizen, Kwanza Price, Nicolas Margot, Jairo M Montezuma-Rusca, Peter Sklar, Martin Rhee, Pedro Cahn

Background: Single-tablet regimens (STRs) revolutionised HIV-1 treatment, improving adherence and clinical outcomes; however, many people cannot take these due to resistance, contraindications, or drug-drug interactions, instead relying on complex multi-tablet regimens. Novel STRs are therefore needed. We aimed to evaluate the efficacy and safety of a novel STR, bictegravir-lenacapavir, in people with HIV-1.

Methods: ARTISTRY-1 was a randomised, open-label, active-controlled, non-inferiority phase 3 trial conducted at hospitals and clinics across 15 countries that enrolled people with HIV-1 with virological suppression on complex regimens. Participants were randomly assigned (using interactive technology, 2:1, stratified by geographical region) to switch to once-daily oral bictegravir-lenacapavir 75 mg/50 mg STR or continued complex regimen. The primary outcome was the proportion of participants with an HIV-1 RNA viral load of 50 copies per mL or higher at week 48 (US Food and Drug Administration Snapshot algorithm), assessed in all randomly assigned participants who received any dose of assigned treatment. This trial (active; enrolment complete) was registered with ClinicalTrials.gov (NCT05502341).

Findings: Between Jan 29 and Sept 26, 2024, 729 participants were screened; 557 were randomly assigned and treated (bictegravir-lenacapavir n=371; complex regimen n=186). At baseline, median age was 60 years (range 22-84), HIV treatment duration was 28 years (IQR 22-32); participants were taking a median of three antiretroviral pills per day (range 2-11). At week 48, an HIV-1 RNA viral load of 50 copies per mL or higher was observed in three (1%) participants receiving bictegravir-lenacapavir and two (1%) receiving a complex regimen (difference -0·3%; 95·002% CI -2·3 to 1·8), meeting the non-inferiority margin of 4%. No resistance emerged. Adverse event rates were similar between groups. Six (2%) participants discontinued bictegravir-lenacapavir and one (1%) discontinued their complex regimen due to adverse events. There were five deaths in the bictegravir-lenacapavir group, none of which were deemed related to study drug. Participants reported increased treatment satisfaction after switching to bictegravir-lenacapavir.

Interpretation: Bictegravir-lenacapavir STR demonstrated non-inferior efficacy to complex regimens, with a similar safety profile and increased treatment satisfaction. Bictegravir-lenacapavir offers new opportunities for HIV-1 treatment optimisation for people taking complex regimens.

Funding: Gilead Sciences.

背景:单片方案(STRs)彻底改变了HIV-1治疗,改善了依从性和临床结果;然而,由于耐药、禁忌症或药物-药物相互作用,许多人不能服用这些药物,而是依赖于复杂的多片方案。因此需要新的str。我们的目的是评估一种新型STR (bictegravir-lenacapavir)在HIV-1患者中的疗效和安全性。ARTISTRY-1是一项随机、开放标签、主动对照、非劣效性的3期试验,在15个国家的医院和诊所进行,招募了采用复杂方案进行病毒学抑制的HIV-1患者。参与者被随机分配(使用交互式技术,2:1,按地理区域分层),切换到每日一次口服bictegravir- lenacapavi75 mg/50 mg STR或继续复杂方案。主要结果是48周时HIV-1 RNA病毒载量为每mL 50拷贝或更高的参与者比例(美国食品和药物管理局快照算法),在所有随机分配的接受任何剂量指定治疗的参与者中进行评估。该试验(正在进行,登记已完成)已在ClinicalTrials.gov注册(NCT05502341)。研究结果:2024年1月29日至9月26日期间,729名参与者接受了筛查;557人被随机分配并接受治疗(bictegravir-lenacapavir n=371;复杂方案n=186)。基线时,中位年龄为60岁(范围22-84),HIV治疗持续时间为28年(IQR 22-32);参与者平均每天服用3粒抗逆转录病毒药物(范围2-11)。在第48周,3名(1%)接受bictegravvir -lenacapavir治疗的参与者和2名(1%)接受复杂治疗的参与者观察到每mL 50拷贝或更高的HIV-1 RNA病毒载量(差异为- 0.3%;95,002% CI -2·3至1.8),符合4%的非劣效性边界。没有出现任何抵抗。两组不良事件发生率相似。6名(2%)参与者因不良事件停用比替格拉韦-lenacapavir, 1名(1%)参与者因不良事件停用复杂方案。bictegravar -lenacapavir组有5例死亡,没有一例被认为与研究药物有关。参与者报告在改用比替格拉韦-lenacapavir后治疗满意度增加。解释:Bictegravir-lenacapavir STR与复杂方案相比显示出不逊色的疗效,具有相似的安全性和更高的治疗满意度。比替格拉韦-lenacapavir为采用复杂方案的患者提供了优化HIV-1治疗的新机会。资助:Gilead Sciences。
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引用次数: 0
Managing complex antiretroviral regimens. 管理复杂的抗逆转录病毒治疗方案。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-25 DOI: 10.1016/S0140-6736(26)00364-8
Michael S Saag
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引用次数: 0
The EAT-Lancet Commission: issues and responses. EAT-Lancet委员会:问题和回应。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-21 DOI: 10.1016/S0140-6736(25)02509-7
Francisco J Zagmutt, Jane G Pouzou, Flaminia Ortenzi, Gordon Guyatt, Andrew Mente, Ty Beal
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引用次数: 0
Health on the front line: 4 years of war in Ukraine. 前线的卫生:乌克兰4年的战争。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-21 DOI: 10.1016/S0140-6736(26)00355-7
The Lancet
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引用次数: 0
The EAT-Lancet Commission: issues and responses. EAT-Lancet委员会:问题和回应。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-21 DOI: 10.1016/S0140-6736(25)02507-3
Robert Fungo, Francis Zotor, Andrew Prentice, Habiba Hassan-Wassef, Muhammad Ali Dhansay, Hassan Aguenaou, Aloysius Maduforo, Kingsley K A Pereko, Given Chipili, Betrand Tambe, Augustin Zeba
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引用次数: 0
Malawi's strategy on childhood non-communicable diseases. 马拉维儿童非传染性疾病战略。
IF 88.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-14 DOI: 10.1016/S0140-6736(25)02632-7
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引用次数: 0
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The Lancet
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