Off-label use of combined antiretroviral therapy, analysis of data collected by the Italian Register for HIV-1 infection in paediatrics in a large cohort of children.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
15 Jan 2022
Historique:
received: 12 03 2021
accepted: 31 12 2021
entrez: 16 1 2022
pubmed: 17 1 2022
medline: 19 1 2022
Statut: epublish

Résumé

Early start of highly active antiretroviral therapy (HAART) in perinatally HIV-1 infected children is the optimal strategy to prevent immunological and clinical deterioration. To date, according to EMA, only 35% of antiretroviral drugs are licenced in children < 2 years of age and 60% in those aged 2-12 years, due to the lack of adequate paediatric clinical studies on pharmacokinetics, pharmacodynamics and drug safety in children. An observational retrospective study investigating the rate and the outcomes of off-label prescription of HAART was conducted on 225 perinatally HIV-1 infected children enrolled in the Italian Register for HIV Infection in Children and followed-up from 2001 to 2018. 22.2% (50/225) of included children were receiving an off-label HAART regimen at last check. Only 26% (13/50) of off-label children had an undetectable viral load (VL) before the commencing of the regimen and the 52.0% (26/50) had a CD4 + T lymphocyte percentage > 25%. At last check, during the off label regimen, the 80% (40/50) of patients had an undetectable VL, and 90% (45/50) of them displayed CD4 + T lymphocyte percentage > 25%. The most widely used off-label drugs were: dolutegravir/abacavir/lamivudine (16%; 8/50), emtricitbine/tenofovir disoproxil (22%; 11/50), lopinavir/ritonavir (20%; 10/50) and elvitegravir/cobicistat/emtricitabine/ tenofovir alafenamide (10%; 10/50). At logistic regression analysis, detectable VL before starting the current HAART regimen was a risk factor for receiving an off-label therapy (OR: 2.41; 95% CI 1.13-5.19; p = 0.024). Moreover, children < 2 years of age were at increased risk for receiving off-label HAART with respect to older children (OR: 3.24; 95% CI 1063-7.3; p = 0.001). Even if our safety data regarding off-label regimens where poor, no adverse event was reported. The prescription of an off-label HAART regimen in perinatally HIV-1 infected children was common, in particular in children with detectable VL despite previous HAART and in younger children, especially those receiving their first regimen. Our data suggest similar proportions of virological and immunological successes at last check among children receiving off-label or on-label HAART. Larger studies are needed to better clarify efficacy and safety of off-label HAART regimens in children, in order to allow the enlargement of on-label prescription in children.

Sections du résumé

BACKGROUND BACKGROUND
Early start of highly active antiretroviral therapy (HAART) in perinatally HIV-1 infected children is the optimal strategy to prevent immunological and clinical deterioration. To date, according to EMA, only 35% of antiretroviral drugs are licenced in children < 2 years of age and 60% in those aged 2-12 years, due to the lack of adequate paediatric clinical studies on pharmacokinetics, pharmacodynamics and drug safety in children.
METHODS METHODS
An observational retrospective study investigating the rate and the outcomes of off-label prescription of HAART was conducted on 225 perinatally HIV-1 infected children enrolled in the Italian Register for HIV Infection in Children and followed-up from 2001 to 2018.
RESULTS RESULTS
22.2% (50/225) of included children were receiving an off-label HAART regimen at last check. Only 26% (13/50) of off-label children had an undetectable viral load (VL) before the commencing of the regimen and the 52.0% (26/50) had a CD4 + T lymphocyte percentage > 25%. At last check, during the off label regimen, the 80% (40/50) of patients had an undetectable VL, and 90% (45/50) of them displayed CD4 + T lymphocyte percentage > 25%. The most widely used off-label drugs were: dolutegravir/abacavir/lamivudine (16%; 8/50), emtricitbine/tenofovir disoproxil (22%; 11/50), lopinavir/ritonavir (20%; 10/50) and elvitegravir/cobicistat/emtricitabine/ tenofovir alafenamide (10%; 10/50). At logistic regression analysis, detectable VL before starting the current HAART regimen was a risk factor for receiving an off-label therapy (OR: 2.41; 95% CI 1.13-5.19; p = 0.024). Moreover, children < 2 years of age were at increased risk for receiving off-label HAART with respect to older children (OR: 3.24; 95% CI 1063-7.3; p = 0.001). Even if our safety data regarding off-label regimens where poor, no adverse event was reported.
CONCLUSION CONCLUSIONS
The prescription of an off-label HAART regimen in perinatally HIV-1 infected children was common, in particular in children with detectable VL despite previous HAART and in younger children, especially those receiving their first regimen. Our data suggest similar proportions of virological and immunological successes at last check among children receiving off-label or on-label HAART. Larger studies are needed to better clarify efficacy and safety of off-label HAART regimens in children, in order to allow the enlargement of on-label prescription in children.

Identifiants

pubmed: 35033018
doi: 10.1186/s12879-022-07026-w
pii: 10.1186/s12879-022-07026-w
pmc: PMC8760752
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

55

Investigateurs

Sara Parigi (S)
Francesca Orlandi (F)
Alessandra de Martino (A)
Raffaella Pinzani (R)
Luisa Abbagnato (L)
Maurizio Ruggeri (M)
Francesco Baldi (F)
Giacomo Faldella (G)
Piergiorgio Chiriacò (P)
Carlo Dessì (C)
Maria Grazia Pantò (MG)
Elisa Anastasio (E)
Maria Rita Govoni (MR)
Maurizio Bigi (M)
Elisabetta Bondi (E)
Riccardo Borea (R)
Giovanni Cenderello (G)
Donato Tommasi (D)
Ernesto Renato Dalle Nogare (ERD)
Marcello Saitta (M)
Leonardo Felici (L)
Rita Consolini (R)
Angelo Antonellini (A)
Gianfranco Anzidei (G)
Orazio Genovese (O)
Salvatore Catania (S)
Fabio Natale (F)
Paolina Olmeo (P)
Letizia Cristiano (L)
Vincenzo Portelli (V)
Marco Rabusin (M)
Giada Maria Di Pietro (GM)
Leone Fabrizio (L)

Informations de copyright

© 2022. The Author(s).

Références

Clin Pharmacokinet. 2016 Feb;55(2):185-96
pubmed: 26245673
Clin Infect Dis. 2011 Aug 1;53(3):310-3
pubmed: 21765089
Medicine (Baltimore). 2015 Oct;94(42):e1677
pubmed: 26496277
Pediatr Med Chir. 2008 Jul-Aug;30(4):177-91
pubmed: 19216201
Antivir Ther. 2016;21(1):65-70
pubmed: 26079937
J Acquir Immune Defic Syndr. 2018 Sep 1;79(1):54-61
pubmed: 29957673
N Engl J Med. 2012 Jun 21;366(25):2380-9
pubmed: 22716976
Expert Rev Clin Pharmacol. 2018 Jan;11(1):83-93
pubmed: 29039686
Antiviral Res. 2010 Jan;85(1):1-18
pubmed: 20018391
Infect Disord Drug Targets. 2018;18(1):15-22
pubmed: 28474549
Medicine (Baltimore). 2016 Jun;95(24):e3842
pubmed: 27310962
BMJ. 2006 May 20;332(7551):1183-7
pubmed: 16709991

Auteurs

Elena Chiappini (E)

Paediatric Infectious Diseases Unit, Department of Health Sciences, Anna Meyer Children's University Hospital, University of Florence, Viale Pieraccini, 24, 50100, Florence, Italy. elena.chiappini@unifi.it.

Catiuscia Lisi (C)

Paediatric Infectious Diseases Unit, Department of Health Sciences, Anna Meyer Children's University Hospital, University of Florence, Viale Pieraccini, 24, 50100, Florence, Italy.

Vania Giacomet (V)

Paediatric Infectious Diseases Unit, Department of Paediatrics, ASST FBF SACCO, University of Milan, Milan, Italy.

Paola Erba (P)

Paediatric Infectious Diseases Unit, Department of Paediatrics, ASST FBF SACCO, University of Milan, Milan, Italy.

Stefania Bernardi (S)

Academic Department of Pediatrics (DPUO), Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Paola Zangari (P)

Academic Department of Pediatrics (DPUO), Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Antonio Di Biagio (A)

Infectious Disease Unit, Ospedale Policlinico San Martino, University of Genova, Genova, Italy.

Lucia Taramasso (L)

Infectious Disease Unit, Ospedale Policlinico San Martino, University of Genova, Genova, Italy.

Carlo Giaquinto (C)

Department of Women and Child Health, University of Padova, Padova, Italy.

Osvalda Rampon (O)

Department of Women and Child Health, University of Padova, Padova, Italy.

Clara Gabiano (C)

Paediatric Infectious Diseases Unit, Regina Margherita Children's Hospital, University of Turin, Turin, Italy.

Silvia Garazzino (S)

Paediatric Infectious Diseases Unit, Regina Margherita Children's Hospital, University of Turin, Turin, Italy.

Claudia Tagliabue (C)

Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Susanna Esposito (S)

Paediatric Clinic, Pietro Barilla Children's Hospital, University of Parma, Parma, Italy.

Eugenia Bruzzese (E)

Department of Translational Medical Sciences, Section of Paediatrics, University of Naples Federico II, Naples, Italy.

Raffaele Badolato (R)

Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.

Domenico Zanaboni (D)

Department On Internal Medicine and Therapeutics, IRCCS Policlinico "S. Matteo" Foundation, University of Pavia, Pavia, Italy.

Monica Cellini (M)

Department of Medical and Surgical Sciences, Section of Paediatric Hemato-Oncology, University of Modena and Reggio Emilia, Modena, Italy.

Maurizio Dedoni (M)

Department of Paediatrics, Ospedale Microcitemico, Cagliari, Italy.

Antonio Mazza (A)

Paediatric Unit, "S. Chiara" Hospital, Trento, Italy.

Andrea Pession (A)

Andrea Pession, Paediatric Unit, IRCCS Azienda Ospedaliero-Universitaria, Bologna, Italy.

Anna Maria Giannini (AM)

Paediatric Infectious Diseases Unit, University Hospital Policlinico Giovanni XXIII, Bari, Italy.

Filippo Salvini (F)

Department of Paediatrics, University of Milan, Niguarda Hospital, Milan, Italy.

Icilio Dodi (I)

Paediatric Clinic, Pietro Barilla Children's Hospital, University of Parma, Parma, Italy.

Ines Carloni (I)

Department of Mother and Child Health, Salesi Children's Hospital, Ancona, Italy.

Salvatore Cazzato (S)

Paediatric Unit, Sant'Anna Hospital, Como, Italy.

Pier Angelo Tovo (PA)

Paediatric Infectious Diseases Unit, Regina Margherita Children's Hospital, University of Turin, Turin, Italy.

Maurizio de Martino (M)

Paediatric Infectious Diseases Unit, Department of Health Sciences, Anna Meyer Children's University Hospital, University of Florence, Viale Pieraccini, 24, 50100, Florence, Italy.

Luisa Galli (L)

Paediatric Infectious Diseases Unit, Department of Health Sciences, Anna Meyer Children's University Hospital, University of Florence, Viale Pieraccini, 24, 50100, Florence, Italy.

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