Surveillance of transmitted drug resistance to integrase inhibitors in Spain: implications for clinical practice.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 06 2019
Historique:
received: 10 11 2018
revised: 17 01 2019
accepted: 24 01 2019
pubmed: 7 3 2019
medline: 21 7 2020
entrez: 7 3 2019
Statut: ppublish

Résumé

Integrase strand-transfer inhibitors (INSTIs) constitute at present one of the pillars of first-line ART. To study the prevalence of and the trend in transmitted drug resistance (TDR) to INSTIs in ART-naive patients in Spain. During the period 2012-17, 1109 patients from CoRIS were analysed. The Stanford algorithm v8.7 was used to evaluate TDR and transmission of clinically relevant resistance. To describe individual mutations/polymorphisms, the most recent IAS list (for INSTIs) and the 2009 WHO list update (for the backbone NRTIs used in combination with INSTIs in first-line treatment) were used. Clinically relevant resistance to the INSTI class was 0.2%: T66I, 0.1%, resistance to elvitegravir and intermediate resistance to raltegravir; and G163K, 0.1%, intermediate resistance to raltegravir and elvitegravir. No clinical resistance to dolutegravir or bictegravir was observed. The prevalence of INSTI TDR following the IAS-USA INSTI mutation list was 2.6%, with no trend towards changes in the prevalence throughout the study period. The overall prevalence of NRTI WHO mutations was 4.3%, whereas clinically relevant resistance to tenofovir, abacavir and emtricitabine/lamivudine was 1.7%, 1.9% and 0.7%, respectively. Given the low prevalence of clinically relevant resistance to INSTIs and first-line NRTIs in Spain, it is very unlikely that a newly diagnosed patient will present with clinical resistance to a first-line INSTI-based regimen. These patients may not benefit from INSTI and NRTI baseline resistance testing.

Sections du résumé

BACKGROUND
Integrase strand-transfer inhibitors (INSTIs) constitute at present one of the pillars of first-line ART.
OBJECTIVES
To study the prevalence of and the trend in transmitted drug resistance (TDR) to INSTIs in ART-naive patients in Spain.
METHODS
During the period 2012-17, 1109 patients from CoRIS were analysed. The Stanford algorithm v8.7 was used to evaluate TDR and transmission of clinically relevant resistance. To describe individual mutations/polymorphisms, the most recent IAS list (for INSTIs) and the 2009 WHO list update (for the backbone NRTIs used in combination with INSTIs in first-line treatment) were used.
RESULTS
Clinically relevant resistance to the INSTI class was 0.2%: T66I, 0.1%, resistance to elvitegravir and intermediate resistance to raltegravir; and G163K, 0.1%, intermediate resistance to raltegravir and elvitegravir. No clinical resistance to dolutegravir or bictegravir was observed. The prevalence of INSTI TDR following the IAS-USA INSTI mutation list was 2.6%, with no trend towards changes in the prevalence throughout the study period. The overall prevalence of NRTI WHO mutations was 4.3%, whereas clinically relevant resistance to tenofovir, abacavir and emtricitabine/lamivudine was 1.7%, 1.9% and 0.7%, respectively.
CONCLUSIONS
Given the low prevalence of clinically relevant resistance to INSTIs and first-line NRTIs in Spain, it is very unlikely that a newly diagnosed patient will present with clinical resistance to a first-line INSTI-based regimen. These patients may not benefit from INSTI and NRTI baseline resistance testing.

Identifiants

pubmed: 30838386
pii: 5369817
doi: 10.1093/jac/dkz067
doi:

Substances chimiques

HIV Integrase Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1693-1700

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Marta Alvarez (M)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

Paz Casas (P)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

Adolfo de Salazar (A)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

Natalia Chueca (N)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

Carlos Guerrero-Beltran (C)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

Carmen Rodríguez (C)

Clínica Sandoval, Madrid, Spain.

Arkaitz Imaz (A)

Unidad de VIH e ITS, Departamento de Enfermedades Infecciosas, Hospital Universitari de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.

Nuria Espinosa (N)

Unidad de Enfermedades Infecciosas, Hospital Virgen del Rocio, Sevilla, Spain.

Silvia García-Bujalance (S)

Unidad de Enfermedades Infecciosas, Hospital Universitario La Paz, Madrid, Spain.

María Jesús Pérez-Elías (MJ)

Unidad de Enfermedades Infecciosas, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Mónica García-Alvarez (M)

Unidad de Microbiología Clínica, Hospital Universitario Doce de Octubre, Madrid, Spain.

Jose Antonio Iribarren (JA)

Unidad de Enfermedades Infecciosas, Hospital Universitario Donostia, Instituto BioDonostia, Donostia, Spain.

Jesús Santos (J)

Unidad de Enfermedades Infecciosas, Hospital Universitario Virgen de la Victoria, Málaga, Spain.

David Dalmau (D)

Unidad de Enfermedades Infecciosas, Hospital Universitario Mutua Terrasa, Terrasa, Spain.

Antonio Aguilera (A)

Servicio y Departamento de Microbiología, Complejo Hospitalario Universitario de Santiago y Universidad de Santiago de Compostela, Santiago de Compostela, Spain.

David Vinuesa (D)

Unidad de Enfermedades Infecciosas, Hospital Universitario, Universitario San Cecilio, Granada, Spain.

Félix Gutiérrez (F)

Unidad de Enfermedades Infecciosas, Hospital Universitario de Elche & Universidad Miguel Hernández, Alicante, Spain.

Beatriz Piérola (B)

Unidad de Enfermedades Infecciosas, Complejo Hospitalario de Navarra, Pamplona, Spain.

José Miguel Molina (JM)

Unidad de Microbiología Clínica, Hospital Universitario La Fe, Valencia, Spain.

Joaquim Peraire (J)

Unidad de Enfermedades Infecciosas, Hospital Universitari de Tarragona Joan XXIII, IISPV, Universitat Rovira i Virgili, Tarragona, Spain.

Irene Portilla (I)

Unidad de Enfermedades Infecciosas, Hospital Universitario Alicante, Alicante, Spain.

Juan Luis Gómez-Sirvent (JL)

Unidad de Enfermedades Infecciosas, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.

Julián Olalla (J)

Unidad de Enfermedades Infecciosas, Hospital Costa del Sol, Marbella, Spain.

Carlos Galera (C)

Unidad de Enfermedades Infecciosas, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.

José Ramón Blanco (JR)

Unidad de Enfermedades Infecciosas, Hospital Universitario San Pedro, Logroño, Spain.

Melchor Riera (M)

Unidad de Enfermedades Infecciosas, Hospital Universitario Son Espases, Palma de Mallorca, Spain.

Lucio García-Fraile (L)

Unidad de Enfermedades Infecciosas, Hospital Universitario La Princesa, Madrid, Spain.

Gemma Navarro (G)

Unidad de Enfermedades Infecciosas, Hospital Universitario Parc Taulí, Sabadell, Spain.

Adrían Curran (A)

Servicio de Enfermedades Infecciosas, Hospital Universitario Vall d´Hebron, Barcelona, Spain.

Eva Poveda (E)

Group of Virology and Pathogenesis, Galicia Sur Health Research Institute (IIS Galicia Sur)-Complexo Hospitalario Universitario de Vigo, SERGAS-UVigo, Spain.

Federico García (F)

Unidad de Microbiología Clínica, Hospital Universitario San Cecilio, Granada, Instituto de Investigacion Ibs., Granada, Spain.

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