Brief Report: Sex Differences in Outcomes for Individuals Presenting for Third-Line Antiretroviral Therapy.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 06 2020
Historique:
pubmed: 13 2 2020
medline: 7 1 2021
entrez: 13 2 2020
Statut: ppublish

Résumé

Sex differences in studies of antiretroviral (ART) drug exposure and treatment outcomes support the hypothesis that some ART combinations may not be well tolerated in women. We evaluated disparities in outcomes between men and women participating in ACTG A5288, an interventional strategy trial for individuals failing a protease inhibitor-based second-line ART regimen in low- and middle-income countries. Participants were assigned to one of 4 cohorts (A-D) based on resistance profiles and ART history. Cohort A had no lopinavir/ritonavir (LPV/r) resistance and stayed on their second-line regimen, and cohorts B, C, and D had increasing resistance and accessed novel ART regimens. In this secondary analysis, we evaluated sex differences in the primary endpoint, HIV-1 RNA ≤200 copies/mL at week 48; confirmed virologic failure ≥1000 copies/mL (VF); and clinical outcomes and adverse events (intent-to-treat). Women made up 258/545 (47%) of the study population. More women than men were assigned to cohort A. Median follow-up was 72 weeks. Fewer women than men had HIV-1 RNA ≤200 copies/mL at week 48: 39% vs. 49% in cohort A and 83% vs. 89% in cohorts B, C, and D combined. More women experienced VF, grade ≥3 signs and symptoms, but similar grade ≥3 diagnoses or laboratory abnormalities. More women than men entered the study with a resistance profile suggesting that their second-line regimen could have been effective in maintaining virologic suppression. The more frequent occurrence of grade ≥3 signs and symptoms in women suggests that tolerability issues were under recognized in women on protease inhibitor-based therapy.

Sections du résumé

BACKGROUND
Sex differences in studies of antiretroviral (ART) drug exposure and treatment outcomes support the hypothesis that some ART combinations may not be well tolerated in women. We evaluated disparities in outcomes between men and women participating in ACTG A5288, an interventional strategy trial for individuals failing a protease inhibitor-based second-line ART regimen in low- and middle-income countries.
METHODS
Participants were assigned to one of 4 cohorts (A-D) based on resistance profiles and ART history. Cohort A had no lopinavir/ritonavir (LPV/r) resistance and stayed on their second-line regimen, and cohorts B, C, and D had increasing resistance and accessed novel ART regimens. In this secondary analysis, we evaluated sex differences in the primary endpoint, HIV-1 RNA ≤200 copies/mL at week 48; confirmed virologic failure ≥1000 copies/mL (VF); and clinical outcomes and adverse events (intent-to-treat).
RESULTS
Women made up 258/545 (47%) of the study population. More women than men were assigned to cohort A. Median follow-up was 72 weeks. Fewer women than men had HIV-1 RNA ≤200 copies/mL at week 48: 39% vs. 49% in cohort A and 83% vs. 89% in cohorts B, C, and D combined. More women experienced VF, grade ≥3 signs and symptoms, but similar grade ≥3 diagnoses or laboratory abnormalities.
CONCLUSIONS
More women than men entered the study with a resistance profile suggesting that their second-line regimen could have been effective in maintaining virologic suppression. The more frequent occurrence of grade ≥3 signs and symptoms in women suggests that tolerability issues were under recognized in women on protease inhibitor-based therapy.

Identifiants

pubmed: 32049773
doi: 10.1097/QAI.0000000000002324
pmc: PMC7228852
mid: NIHMS1558587
pii: 00126334-202006010-00010
doi:

Substances chimiques

Anti-HIV Agents 0
Drug Combinations 0
Reverse Transcriptase Inhibitors 0
lopinavir-ritonavir drug combination 0
Lopinavir 2494G1JF75
Ritonavir O3J8G9O825

Banques de données

ClinicalTrials.gov
['NCT01641367']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

203-207

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI069423
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069481
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106701
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI108568
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106716
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI045008
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States

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Auteurs

Catherine Godfrey (C)

Division of AIDS NIAID, NIH, Bethesda, MD.

Michael D Hughes (MD)

Harvard T.H. Chan School of Public Health, Boston, MA.

Justin Ritz (J)

Harvard T.H. Chan School of Public Health, Boston, MA.

Lara Coelho (L)

Instituto Nacional de Infectologia Evandro Chagas, Rio de Janeiro, Brazil.

Robert Gross (R)

University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Robert Salata (R)

Case Western Reserve University School of Medicine, Cleveland, OH.

Rosie Mngqibisa (R)

Durban International CRS, Enhancing Care Foundation, Durban, South Africa.

Carole L Wallis (CL)

Lancet Laboratories and BARC SA, Johannesburg, South Africa.

Makanga E Mumbi (ME)

KEMRI Centre for Global Health Research, Kisumu, Kenya.

Mitch Matoga (M)

UNC Project, Lilongwe, Malawi.

Selvamuthu Poongulali (S)

CART Clinical Research Site, Voluntary Health Services, Chennai, India.

Marije Van Schalkwyk (M)

FAM-CRU CRS, Stellenbosch University, Cape Town, South Africa.

Evelyn Hogg (E)

Social & Scientific Systems, Silver Spring, MD.

Courtney V Fletcher (CV)

University of Nebraska Medical Center, Omaha, NE; and.

Beatriz Grinsztejn (B)

Instituto Nacional de Infectologia Evandro Chagas, Rio de Janeiro, Brazil.

Ann C Collier (AC)

University of Washington School of Medicine, Seattle, WA.

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Classifications MeSH