Journal Article

Lopinavir/Ritonavir Monotherapy as a Nucleoside Analogue—Sparing Strategy to Prevent HIV-1 Mother-to-Child Transmission: The ANRS 135 PRIMEVA Phase 2/3 Randomized Trial

Treluyer, Jean-Marc, Chaix, Marie-Laure, Le Chenadec, Jérome, Ekoukou, Dieudonné, Tubiana, Roland, Delmas, Sandrine, Bui, Eda, Warszawski, Josiane, Mandelbrot, Laurent, Hirt, Deborah, Rouzioux, Christine, Blanche, Stéphane

2013

Overview

Background. Prevention of mother-to-child transmission (PMTCT) of human immunodeficiency virus (HIV) is usually based on zidovudine-containing regimens, despite potential toxicities. This multicenter trial evaluated whether lopinavir/ritonavir (LPV/r) monotherapy in HIV type 1—infected women not requiring antiretrovirals for themselves could control maternal viral load (VL). Methods. Overall, 105 pregnant women with baseline VL <30 000 copies/mL and CD4 ≥350 cells/μL were randomized to start open-label LPV/r 400/100 mg twice daily alone (monotherapy group, n = 69) or combined with zidovudine/lamivudine 300/150 mg twice daily (triple therapy group, n = 36) from 26 gestational weeks to delivery. According to a Fleming 2-stage phase 2 design, monotherapy was considered to be efficacious if at least 59 patients achieved VL <200 copies/mL at 8 weeks of treatment (primary endpoint). Secondary endpoints were VL at delivery and tolerance. Results. Monotherapy was efficacious as defined: 62 women in the monotherapy group achieved VL <200 copies/mL at 34 weeks' gestation (ie, 8 weeks of treatment; 89.9%; 95% confidence interval [CI], 80.2%–95.8%). At delivery, proportions with VL <200 copies/mL were similar in the monotherapy and triple therapy groups (92.8% vs 97.2%; P = .66); however, fewer had VL <50 copies/mL in the monotherapy group (78.3% vs 97.2%; P = .01). Changes for intolerance were less frequent in the monotherapy than in the triple therapy group (1.4% vs 11.1%, respectively; P = .046). Cesarean delivery and preterm delivery rates did not differ. All children were liveborn; 1 case of HIV-1 transmission occurred in the triple therapy group, none in the monotherapy group (95% CI upper limit = 5.2%). Conclusions. LPV/r monotherapy achieved satisfactory virologic efficacy in women treated solely for PMTCT, providing proof of concept for future nucleoside-sparing strategies. Clinical Trials Registration. NCT00424814; Afssaps AIDS Clinical Trial Group A61176-34.

• Publisher: Oxford University Press
• Subject: Adolescent / Adult / AIDS / Anti-HIV Agents - therapeutic use / Antibiotics. Antiinfectious agents. Antiparasitic agents / Antiretroviral drugs / Antiretrovirals / Antiviral agents / Biological and medical sciences / Children / Clinical outcomes / Disease transmission / Female / HIV / HIV 1 / HIV Infections - drug therapy / HIV Infections - prevention & control / HIV Infections - transmission / HIV/AIDS / Human immunodeficiency virus / Human viral diseases / Humans / Immunodeficiencies / Immunodeficiencies. Immunoglobulinopathies / Immunology / Immunopathology / Infant, Newborn / Infants / Infectious Disease Transmission, Vertical - prevention & control / Infectious diseases / Lopinavir - therapeutic use / Male / Maternal & child health / Medical sciences / Pharmacology. Drug treatments / Pregnancy / Pregnancy Complications, Infectious - drug therapy / Pregnancy Complications, Infectious - prevention & control / Pregnancy Complications, Infectious - virology / Ritonavir / Ritonavir - therapeutic use / Statistical median / Test ranges / Viral diseases / Viral diseases of the lymphoid tissue and the blood. Aids / Virology