ViiV Healthcare近期宣布,其3期LATITUDE臨床試驗的最終結果顯示,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優于每日口服抗逆轉錄病毒治療(ART),尤其是在既往治療依從性困難的人群中。該研究的48周數據已發表于《新英格蘭醫學雜志》(
NEJM)。
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LATITUDE是一項隨機、開放標簽的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失敗與因任何原因導致的方案中止的綜合指標。結果顯示,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險為22.8%(29/152),而繼續每日口服ART治療人群為41.2%(55/154),風險降低近一半。該研究結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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