Long-acting injections of cabotegravir (CAB) plus rilpivirine (RPV) is recommended in US and EU treatment guidelines based on two-monthly IM dosing.
CAB/RPV-LA is already available in Scotland and will soon be available in the rest of the UK. Long-acting therapies have many potential benefits, but drug resistance has been highlighted by BHIVA and others despite full adherence. [1, 2]
CROI 2022 included a poster of year three results from the ATLAS-2M phase 3b non-inferiority ITT-E study [2]. Participants were randomised to receive injections every four (Q4W, n=523) or eight weeks (Q8W, n=522). Participants on this multicentre study (Argentina, Australia, Canada, Europe, Korea, Mexico, Russia, South Africa and USA) were women (27%, n=280), median age 42 years (range: 19 to 83), white (73%), BMI >30 kg/m2 (20%); 37% had previous exposure to CAB/RPV.
Non-inferiority of Q4W vs Q8W was reported based on the primary endpoint detectable viral load (>50 copies/mL at week 48) and efficacy remains high at week 152 (86-87%).
Non-inferiority was confirmed between Q4W and Q8W regimens within 4% and 10% margins for detectable and undetectable viral load, respectively. This was 3% (n=14, Q8W) vs 1% (n=5, Q4W) in the ITT-E analysis. Withdrawal rates were higher in Q4W (18%) vs Q4W (14%) with participants citing frequency of visits and intolerability of injections.
Total confirmed virologic failure (CVF) occurred in 11 and 2 for Q8W and Q4W, respectively, with two new CVF between weeks 96 to 152 on Q8W. Both participants developed resistance associated mutations to both CAB and RPV, despite perfect protocol adherence. Viral suppression with alternative ART was achieved.
Adverse events were similar to week 96 results.
Two new low-grade drug-related (non-ISR) adverse events were reported (lipoatrophy and pyrexia).
Treatment satisfaction scores were higher for Q8W than Q4W regimens (p=0.004)
This study confirms previous safety and efficacy data supporting a Q8W strategy. The mechanism to explain drug resistance despite perfect adherence to treatment has not been explained. This could include potential differences in interpatient PK related to injection technique. [4]
Other posters at CROI 2022 include early results from a phase 1/2 PK study in 23 adolescents adding either cabotegravir or rilpivirine to current active ART. Both involved oral formulations before the IM injections and reported comparable drugs levels to adults. [5]
There were 2/23 discontinuations, both in the rilpivirine group. One was due to a hypersensitivity reaction to the first oral dose and one due to pain from the needle, before the full injection.
Another poster used PK/PD modelling to predict that dose adjustment should not be needed during pregnancy. [6]
By Kirk Taylor, HIV i-Base
References
Source : HIV i-Base
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