Emergent Resistance to Dolutegravir Among INSTI-Naïve Patients on First-line or Second-line Antiretroviral Therapy: A Review of Published Cases.

HIV dolutegravir resistance treatment failure treatment-naïve

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 17 01 2020
accepted: 28 05 2020
entrez: 27 6 2020
pubmed: 27 6 2020
medline: 27 6 2020
Statut: epublish

Résumé

None of the licensing studies of dolutegravir (DTG) reported any treatment-emergent resistance among DTG-treated individuals, though virological failure in treatment-naïve and treatment-experienced, integrase strand transfer inhibitor (INSTI)-naïve individuals has been reported in clinical practice. While the spectrum of dolutegravir-selected mutations and their effects on clinical outcome have been described, the clinical characteristics of these rare but important virological failure cases are often overlooked. In this perspective piece, we focus on key clinical aspects of emergent resistance to DTG among treatment-naïve and treatment-experienced INSTI-naïve patients, with an aim to inform clinical decision-making. Poor adherence and HIV disease factors contribute to emergent drug resistance, even in regimens with high resistance barriers. Patients with severe immunosuppression or poor adherence are under-represented in licensing studies, and these patients may be at higher risk of treatment failure with DTG resistance, which requires close clinical and laboratory follow-up.

Identifiants

pubmed: 32587877
doi: 10.1093/ofid/ofaa202
pii: ofaa202
pmc: PMC7304932
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofaa202

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Références

Sex Transm Infect. 2018 Sep;94(6):420
pubmed: 30030303
N Engl J Med. 2019 Aug 29;381(9):816-826
pubmed: 31339676
Pharmacotherapy. 2017 Aug;37(8):e82-e89
pubmed: 28556353
Lancet Infect Dis. 2019 Mar;19(3):253-264
pubmed: 30732940
Pediatr Infect Dis J. 2015 Nov;34(11):1207-13
pubmed: 26244832
Clin Infect Dis. 2018 May 17;66(11):1794-1797
pubmed: 29293895
Expert Opin Drug Metab Toxicol. 2013 Sep;9(9):1067-84
pubmed: 23682923
Open Forum Infect Dis. 2018 Dec 10;6(1):ofy332
pubmed: 30631792
PLoS One. 2013 Nov 08;8(11):e79603
pubmed: 24282510
N Engl J Med. 2019 Aug 29;381(9):887-889
pubmed: 31461601
AIDS. 2017 Jun 19;31(10):1425-1434
pubmed: 28375875
Lancet. 2019 Jan 12;393(10167):143-155
pubmed: 30420123
Virology. 1997 Nov 24;238(2):231-42
pubmed: 9400596
Clin Infect Dis. 2018 Aug 16;67(5):791-794
pubmed: 29933437
Antiviral Res. 2020 Jul;179:104717
pubmed: 31982483
Braz J Infect Dis. 2003 Feb;7(1):16-22
pubmed: 12807688
J Antimicrob Chemother. 2019 Nov 1;74(11):3135-3149
pubmed: 31280314
Clin Infect Dis. 2020 Feb 3;70(4):549-556
pubmed: 30918967
Lancet. 2013 Aug 24;382(9893):700-8
pubmed: 23830355

Auteurs

Muge Cevik (M)

Infection and Global Health Research, School of Medicine, University of St Andrews, St Andrews, UK.
NHS Lothian Infection Service, Specialist Virology Laboratory, Royal Infirmary of Edinburgh, Edinburgh, UK.

Chloe Orkin (C)

Blizzard Institute, Queen Mary University of London, London, UK.
Royal London Hospital, Barts Health NHS Trust, London, UK.

Paul E Sax (PE)

Division of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Harvard Medical School, Boston, Massachusetts, USA.

Classifications MeSH