Resistance analyses in highly treatment-experienced people with human immunodeficiency virus (HIV) treated with the novel capsid HIV inhibitor lenacapavir
NA Margot, V Naik, L VanderVeen… - The Journal of …, 2022 - academic.oup.com
NA Margot, V Naik, L VanderVeen, O Anoshchenko, R Singh, H Dvory-Sobol, MS Rhee…
The Journal of Infectious Diseases, 2022•academic.oup.comBackground Lenacapavir (LEN) is a first-in-class inhibitor of human immunodeficiency virus
type 1 (HIV-1) capsid function in clinical development for the treatment of heavily treatment-
experienced (HTE) people with HIV (PWH) harboring multidrug resistance (MDR) in
combination with an optimized background regimen (OBR). Here we describe resistance
analyses conducted in the pivotal phase 2/3 CAPELLA study. Methods CAPELLA enrolled
viremic HTE PWH with resistance to≥ 3 of 4 of the main antiretroviral (ARV) classes and …
type 1 (HIV-1) capsid function in clinical development for the treatment of heavily treatment-
experienced (HTE) people with HIV (PWH) harboring multidrug resistance (MDR) in
combination with an optimized background regimen (OBR). Here we describe resistance
analyses conducted in the pivotal phase 2/3 CAPELLA study. Methods CAPELLA enrolled
viremic HTE PWH with resistance to≥ 3 of 4 of the main antiretroviral (ARV) classes and …
Background
Lenacapavir (LEN) is a first-in-class inhibitor of human immunodeficiency virus type 1 (HIV-1) capsid function in clinical development for the treatment of heavily treatment-experienced (HTE) people with HIV (PWH) harboring multidrug resistance (MDR) in combination with an optimized background regimen (OBR). Here we describe resistance analyses conducted in the pivotal phase 2/3 CAPELLA study.
Methods
CAPELLA enrolled viremic HTE PWH with resistance to ≥3 of 4 of the main antiretroviral (ARV) classes and resistance to ≥2 ARV drugs per class. Baseline resistance analyses used commercial assays (HIV-1 protease, reverse transcriptase, integrase genotypic/phenotypic tests). Postbaseline resistance was evaluated in participants experiencing virologic failure.
Results
At baseline, 46% of participants had resistance to the 4 main ARV drug classes, with one-third of participants having exhausted all drugs from ≥3 of the 4 main ARV classes. Treatment with LEN + OBR for 26 weeks led to viral suppression in 81% of participants. Postbaseline resistance mutations to lenacapavir occurred in 8 participants (6 with M66I, 1 with K70H, 1 with Q67H + K70R) who were receiving unintended functional LEN monotherapy at the time of resistance selection.
Conclusions
LEN added to OBR led to high efficacy in this HTE patient population with MDR but could select for resistance when used unintentionally as functional monotherapy.
Oxford University Press