ViiV Healthcare, Durham, North Carolina, USA.
ViiV Healthcare, Madrid, Spain.
HIV Med. 2023 Feb;24(2):202-211. doi: 10.1111/hiv.13370. Epub 2022 Aug 9.
Physicians could request compassionate use of oral and long-acting (LA) cabotegravir + rilpivirine for people living with HIV-1 under a single-patient request programme supported by ViiV Healthcare and Janssen. Outcomes are reported.
Eligibility criteria included need for parenteral therapy, no primary resistance mutations to cabotegravir or rilpivirine, and established retention in care. Demographic, efficacy, and safety data were obtained from standardized programme applications and quarterly clinical updates. Individuals received a loading dose of LA cabotegravir 600 mg + rilpivirine 900 mg, followed by LA maintenance doses of 400 mg/600 mg every 4 weeks; some received lead-in oral cabotegravir and rilpivirine.
Through July 2020, 35 people living with HIV-1 had data available. The most frequent reason for compassionate use request was chronic non-adherence due to psychological conditions (n = 15). Of 35 people living with HIV-1, 28 had detectable viremia (median viral load 60 300 copies/mL) and seven were virologically suppressed at programme entry; 16/28 and 6/7 achieved or maintained virological suppression at data cutoff, respectively. Seven people living with HIV-1 discontinued for incomplete virological response, six with detectable viremia at initiation; six and four had new reverse transcriptase and integrase mutations at discontinuation, respectively. Six non-fatal serious adverse events were reported, two considered possibly treatment related. Four deaths were reported; none were treatment related. One individual reported two pregnancies and continued LA dosing.
Most people living with HIV-1 had advanced disease and achieved (16/28) or maintained (6/7) virological suppression with LA therapy. Cabotegravir LA + rilpivirine LA as compassionate use provided a valuable treatment option for individuals with adherence issues with oral therapy and advanced disease.
在 ViiV 医疗保健公司和杨森公司支持的单一患者申请计划下,医生可以为感染 HIV-1 的患者申请同情用药,使用口服和长效(LA)卡替拉韦/利匹韦林。现将结果报告如下。
入选标准包括需要进行注射治疗、无卡替拉韦或利匹韦林原发性耐药突变,以及已建立的治疗保留。从标准化的项目申请和每季度的临床更新中获取人口统计学、疗效和安全性数据。患者接受 LA 卡替拉韦 600 mg + 利匹韦林 900 mg 的负荷剂量,随后每 4 周接受 LA 维持剂量 400 mg/600 mg;部分患者接受口服卡替拉韦和利匹韦林的导入治疗。
截至 2020 年 7 月,共有 35 名 HIV-1 感染者的数据可用。同情用药申请最常见的原因是由于心理状况导致的慢性不依从(n=15)。在 35 名 HIV-1 感染者中,28 人有可检测到的病毒血症(中位病毒载量 60300 拷贝/ml),7 人在项目开始时病毒学抑制;分别有 16/28 和 6/7 在数据截止时达到或维持病毒学抑制。7 名患者因不完全病毒学应答而停药,6 名患者在开始时病毒载量可检测;6 名和 4 名患者在停药时分别出现新的逆转录酶和整合酶突变。报告了 7 例非致命性严重不良事件,其中 2 例被认为可能与治疗相关。报告了 4 例死亡;均与治疗无关。1 名患者报告了两次怀孕,并继续接受 LA 治疗。
大多数 HIV-1 感染者疾病进展严重,但 LA 治疗后(16/28)或维持(6/7)病毒学抑制。卡替拉韦 LA+利匹韦林 LA 作为同情用药为口服治疗依从性差和疾病进展严重的患者提供了一种有价值的治疗选择。