Treatment-Experienced Patients on Third-Line Therapy : A Retrospective Cohort of Treatment Outcomes at the HIV Advanced Treatment Centre, University Teaching Hospital, Zambia

Antiretroviral therapy (ART) uptake continues to increase across sub-Saharan Africa and emergence of drug-resistant HIV mutations poses significant challenges to management of treatment-experienced patients with virologic failure. In Zambia, new third-line ART (TLART) guidelines including use of dolutegravir (DTG) were introduced in 2018. We assessed virologic suppression, immunologic response, and HIV drug-resistant mutations (DRMs) among patients on TLART at the University Teaching Hospital (UTH) in Lusaka, Zambia. We conducted a retrospective review of patients enrolled at UTH on TLART for >6 months between January 2010 and June 30, 2021. CD4 and HIV viral load (VL) at TLART initiation and post-initiation were assessed to determine virologic and immunologic outcomes. Regression analysis using bivariate and multivariate methods to describe baseline characteristics, virologic, and immunologic response to TLART was performed. A total of 345 patients met inclusion criteria; women comprised 57.6% (199/345) of the cohort. Median age at HIV diagnosis was 30 (interquartile range: 17.3-36.8). In 255 (73.8%) patients with at least two VLs, VL decreased from mean of 3.45 log10 copies/mL (standard deviation [SD]: 2.02) to 1.68 log10 copies/mL (SD: 1.79). Common ARVs prescribed included DTG (89.9%), tenofovir disoproxil fumarate (68.7%), and darunavir boosted with ritonavir (66.4%); 170 (49.3%) patients had genotypes; mutations consisted of 88.8% nucleoside reverse transcriptase inhibitor, 86.5% non-nucleoside reverse transcriptase inhibitor, and 55.9% protease inhibitor. VL suppression to <1,000 copies/mL was achieved in 225 (78.9%) patients. DRM frequency ranged from 56% to 89% depending on drug class. Treatment-experienced patients receiving TLART in Zambia achieved high rates of suppression despite high proportions of HIV mutations illustrating TLART effectiveness in the DTG era.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:38

Enthalten in:

AIDS research and human retroviruses - 38(2022), 10 vom: 04. Okt., Seite 798-805

Sprache:

Englisch

Beteiligte Personen:

Toeque, Mona-Gekanju [VerfasserIn]
Lindsay, Brianna [VerfasserIn]
Zulu, Paul Msanzya [VerfasserIn]
Hachaambwa, Lottie [VerfasserIn]
Fwoloshi, Sombo [VerfasserIn]
Chanda, Duncan [VerfasserIn]
Stafford, Kristen A [VerfasserIn]
Mupeta, Francis [VerfasserIn]
Siwingwa, Mpanji [VerfasserIn]
Mutinta, Melody [VerfasserIn]
Chirwa, Lameck [VerfasserIn]
Riedel, David J [VerfasserIn]
Claassen, Cassidy [VerfasserIn]
Mulenga, Lloyd [VerfasserIn]

Links:

Volltext

Themen:

99YXE507IL
Anti-HIV Agents
Antiretroviral treatment
Darunavir
HIV
Journal Article
O3J8G9O825
Protease Inhibitors
Research Support, Non-U.S. Gov't
Reverse Transcriptase Inhibitors
Ritonavir
Sub-Saharan Africa
Tenofovir
Third-line ART
Virologic failure
YO603Y8113
Zambia

Anmerkungen:

Date Completed 20.10.2022

Date Revised 24.01.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1089/AID.2021.0208

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM342996053