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Switching to Doravirine in cART-Experienced Patients: An Effective and Highly Tolerated Option With Substantial Cost Savings.
Lanting, Vincent R; Oosterhof, Piter; Ait Moha, Daoud; van Heerde, Roos; Kleene, Marie José T; Stalenhoef, Janneke E; de Regt, Marieke J A; Vrouenraets, Saskia M E; van den Berk, Guido E L; Brinkman, Kees.
Afiliação
  • Lanting VR; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • Oosterhof P; Department of Clinical Pharmacology, OLVG Hospital, Amsterdam, the Netherlands.
  • Ait Moha D; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • van Heerde R; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • Kleene MJT; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • Stalenhoef JE; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • de Regt MJA; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • Vrouenraets SME; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • van den Berk GEL; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
  • Brinkman K; Department of Internal Medicine, OLVG Hospital, Amsterdam, the Netherlands; and.
J Acquir Immune Defic Syndr ; 95(2): 190-196, 2024 02 01.
Article em En | MEDLINE | ID: mdl-37963350
BACKGROUND: Doravirine is a non-nucleoside reverse transcriptase inhibitor with demonstrated efficacy as a third agent in treatment-naive and treatment-experienced people living with HIV (PLWH) in registration studies. However, limited real-world data are available. METHODS: By searching electronic health care records, PLWH using doravirine-based regimens were selected with at least 1 year of follow-up after their first prescription. All stable PLWH who were switched to a doravirine-based regimen were included in the analysis. The primary outcome was the durability of a doravirine-based regimen 1 year after prescription. Reasons for stopping were also collected. Secondary outcomes for PLWH continuing a doravirine-based regimen after 1 year were routine laboratory assessment, body mass index, and differences in medication costs compared with their previous cART. RESULTS: A total of 687 patients (92% men) were included from September 2019 to August 2022: 97.7% switched to doravirine/tenofovir/lamivudine (DOR/TDF/3TC). After 1 year, 94/687 (13.6%) PLWH stopped this therapy. The main reason for discontinuation was patient-reported adverse events in 70/687 (10.2%). Medical reasons for discontinuation included increased alanine tranaminase levels in 6/687 (0.9%), decreased estimated glomerular filtration rate in 3/687 (0.4%), and precautions after diagnosis of osteoporosis in 2/687 (0.3%) patients. Virologic failure occurred in 4/687 cases (0.6%), and 1 case demonstrated resistance mutations. The secondary outcomes demonstrated a statistically significant increase in alanine tranaminase levels and decrease in LDL-c levels. The switch to a doravirine-based regimen in the Netherlands reduced medication costs by 27%. CONCLUSIONS: This study demonstrated that switching to a doravirine-based regimen, mostly DOR/TDF/3TC, was highly effective and generally well tolerated, with substantial cost savings.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Piridonas / Triazóis / Infecções por HIV / Fármacos Anti-HIV Limite: Female / Humans / Male Idioma: En Revista: J Acquir Immune Defic Syndr Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Piridonas / Triazóis / Infecções por HIV / Fármacos Anti-HIV Limite: Female / Humans / Male Idioma: En Revista: J Acquir Immune Defic Syndr Ano de publicação: 2024 Tipo de documento: Article