Changing antiretroviral therapy to dolutegravir from a ritonavir-boosted protease inhibitor in patients with virologic suppression is safe, even without resistance genotyping.
Dolutegravir-based antiretroviral therapy (whether initial or second line) is preferred in most of the world. In sub-Saharan Africa, most persons with HIV (PWH) who have failed initial therapy are receiving ritonavir-boosted protease inhibitor (PI)–based therapy. In a trial in Kenya, investigators studied the efficacy of switching (in the absence of genotypic resistance data) previously treated PWH with viral suppression on a ritonavir-boosted PI regimen to a dolutegravir-based regimen. The baseline nucleoside reverse transcriptase inhibitor (NRTI) backbone was maintained in all participants. The primary endpoint was virologic failure at week 48 (defined as viral loads ≥50 copies/mL).
Of 795 participants, about half were randomized to switch…
Reviewing Author
DisclosuresGrant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; NIH/National Institute on Drug Abuse
Editorial BoardsJAIDS: Journal of Acquired Immune Deficiency Syndromes; Vaccines
Leadership Positions in Professional SocietiesInternational Antiviral Society–USA (Board of Directors); Infectious Diseases Society of America (Past President)
DisclosuresGrant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; NIH/National Institute on Drug Abuse
Editorial BoardsJAIDS: Journal of Acquired Immune Deficiency Syndromes; Vaccines
Leadership Positions in Professional SocietiesInternational Antiviral Society–USA (Board of Directors); Infectious Diseases Society of America (Past President)