Real World Use of Lenacapavir, as an add-on to an Optimized Background Regimen in France

For most people with human immunodeficiency virus type 1 (HIV-1) infection, an effective antiretroviral regimen can be devised. However, some PWH have multiple treatment failures due to viral resistance or unacceptable side effects to medication and no longer have durable viral suppression. People with multidrug-resistant HIV-1 are at increased risk for hospitalization, progression to acquired immunodeficiency syndrome, and death.

Lenacapavir (LEN) is a first-in-class inhibitor of HIV-1 capsid function.5 By interfering with capsid-mediated nuclear uptake of pre-integration complexes and impairing virion production, lenacapavir inhibits viral replication at both early and late stages of the life cycle. In vitro, lenacapavir has antiviral activity against viral mutations that are resistant to major antiretroviral classes of drugs. LEN can be administered in a long-acting fashion - up to every 6 months subcutaneously or weekly orally - because of its picomolar potency, low clearance, and slow release kinetics. Its efficacy has been demonstrated in the CAPELLA phase 3 trial. For the primary endpoint (following 14 days of functional monotherapy) of CAPELLA, 88% of participants randomized to LEN achieved a significant viral load reduction (≥0.5 log10 copies/mL decline) versus 17% on placebo (p\< 0.001).10 Consistent with results through week 52 of the CAPELLA study, LEN combined with an optimized background regimen (OBR) continued to result in high and sustained rates of virologic suppression and increases in CD4 T cell counts through week. When analyzed as missing equals excluded, 82% of participants achieved HIV-1 RNA \<50 copies/mL.

Lenacapavir has become publicly available in France in June 20, 2023. LEN prescriptions in France are discussed and validated by multidisciplinary committees, including HIV physicians, virologists and pharmacologists in the hospitals.

From the time LEN was made publicly available in France, no real-world data have been generated (except for a few clinical cases) to describe the real-world use of LEN, in association with an OBR, in various patient's profiles who may differ from the subjects included the CAPELLA trial.

To document the real-world use of LEN plus OBR, this study will describe baseline socio-demographic, clinical and biological profiles of PWH receiving LEN with OBR, and determine the continuation of LEN injections at week 26 and week 52 in real-life settings in France.

In its current indication, LEN is reserved for a minority of PWH. However, France is the second-largest prescribing country for this drug, and one year after it was first marketed, it seems essential to review its use. Whether LEN injections are continued 6 and 12 months after starting treatment is a crucial question for understanding its use in treatment centers.

LENAddOn is a retrospective, observational, national, multicenter study

This study consists in retrospectively analyzing data from participant medical records, without intervention. All clinical decisions are made as part of routine management, and are not protocolized. No additional clinical visits or biological samples are required for the study. For this reason, weeks 26 and 52 are for information only, but a window of +/- 2 weeks will be allowed for data capture. Initiation of LEN and optimization of associated ART is chosen by the physician, in agreement with the patient, after discussion within a multidisciplinary committee, as recommended by the guidelines. All these decisions are independent of the LENAddOn observational study.

All participants to be included in the study have already begun their LEN treatment, since the period for initiating LEN (first dose received) has ended (end of June 2024). They will be therefore identified retrospectively for inclusion in the study. Some patients will not have completed their 52-week follow-up at the time of inclusion in the study: their follow-up will be prospective. Nevertheless, data collection will be retrospective. Entry of participants' data into the eCRF will only be authorized for a period of time following the end of the follow-up period for the last patient included.