ViiV Healthcare近期宣布,其3期LATITUDE臨床試驗的最終結(jié)果顯示,長效注射型HIV治療方案Cabenuva(cabotegravir + rilpivirine)在維持病毒載量抑制方面的表現(xiàn)優(yōu)于每日口服抗逆轉(zhuǎn)錄病毒治療(ART),尤其是在既往治療依從性困難的人群中。該研究的48周數(shù)據(jù)已發(fā)表于《新英格蘭醫(yī)學(xué)雜志》(
NEJM)。
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LATITUDE是一項隨機、開放標(biāo)簽的3期研究,共納入453名難以堅持每日口服ART或曾中斷HIV醫(yī)療管理的受試者,旨在評估長效治療方案在真實世界場景中的治療益處。研究的主要終點為兩組治療方案的治療失敗率比較,治療失敗定義為病毒學(xué)失敗與因任何原因?qū)е碌姆桨钢兄沟木C合指標(biāo)。結(jié)果顯示,在48周治療期間,接受長效注射Cabenuva方案的患者累計治療失敗風(fēng)險為22.8%(29/152),而繼續(xù)每日口服ART治療人群為41.2%(55/154),風(fēng)險降低近一半。該研究結(jié)果進一步支持長效注射治療在改善依從性困難患者治療結(jié)局方面的潛力,提示其有望成為特定HIV患者群體的治療選擇。
參考資料:
[1] ViiV Healthcare’s long-acting Cabenuva (cabotegravir + rilpivirine) for HIV demonstrates superior efficacy compared to daily oral therapy for people with adherence challenges; results published in NEJM. Retrieved February 20, 2026 from https://www.businesswire.com/news/home/20260218371644/en/ViiV-Healthcares-long-acting-Cabenuva-cabotegravir-rilpivirine-for-HIV-demonstrates-superior-efficacy-compared-to-daily-oral-therapy-for-people-with-adherence-challenges-results-published-in-NEJM
[2] CALQUENCE? plus venetoclax approved in the US as first all-oral, fixed-duration combination for patients with chronic lymphocytic leukemia in the 1st-line setting. Retrieved February 20, 2026 from https://www.businesswire.com/news/home/20260220286386/en/CALQUENCE-plus-venetoclax-approved-in-the-US-as-first-all-oral-fixed-duration-combination-for-patients-with-chronic-lymphocytic-leukemia-in-the-1st-line-setting
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