Publicación:
Single-dose tafenoquine to prevent relapse of plasmodium vivax malaria

dc.contributor.authorLacerda, M.V.G.
dc.contributor.authorLlanos Cuentas, Elmer Alejandro
dc.contributor.authorKrudsood, S.
dc.contributor.authorLon, C.
dc.contributor.authorSaunders, D.L.
dc.contributor.authorMohammed, R.
dc.contributor.authorYilma, D.
dc.contributor.authorPereira, D.B.
dc.contributor.authorEspino, F.E.J.
dc.contributor.authorMia, R.Z.
dc.contributor.authorChuquiyauri, R.
dc.contributor.authorVal, F.
dc.contributor.authorCasapía, M.
dc.contributor.authorMonteiro, W.M.
dc.contributor.authorBrito, M.A.M.
dc.contributor.authorCosta, M.R.F.
dc.contributor.authorBuathong, N.
dc.contributor.authorNoedl, H.
dc.contributor.authorDiro, E.
dc.contributor.authorGetie, S.
dc.contributor.authorWubie, K.M.
dc.contributor.authorAbdissa, A.
dc.contributor.authorZeynudin, A.
dc.contributor.authorAbebe, C.
dc.contributor.authorTada, M.S.
dc.contributor.authorBrand, F.
dc.contributor.authorBeck, H.-P.
dc.contributor.authorAngus, B.
dc.contributor.authorDuparc, S.
dc.contributor.authorKleim, J.-P.
dc.contributor.authorKellam, L.M.
dc.contributor.authorRousell, V.M.
dc.contributor.authorJones, S.W.
dc.contributor.authorHardaker, E.
dc.contributor.authorMohamed, K.
dc.contributor.authorClover, D.D.
dc.contributor.authorFletcher, K.
dc.contributor.authorBreton, J.J.
dc.contributor.authorUgwuegbulam, C.O.
dc.contributor.authorGreen, J.A.
dc.contributor.authorKoh, G.C.K.W.
dc.date.accessioned2026-04-28T22:47:52Z
dc.date.issued2019
dc.description.abstractBACKGROUND: Treatment of Plasmodium vivax malaria requires the clearing of asexual parasites, but relapse can be prevented only if dormant hypnozoites are cleared from the liver (a treatment termed "radical cure"). Tafenoquine is a single-dose 8-aminoquinoline that has recently been registered for the radical cure of P. vivax. METHODS: This multicenter, double-blind, double-dummy, parallel group, randomized, placebo-controlled trial was conducted in Ethiopia, Peru, Brazil, Cambodia, Thailand, and the Philippines. We enrolled 522 patients with microscopically confirmed P. vivax infection (>100 to <100,000 parasites per microliter) and normal glucose-6-phosphate dehydrogenase (G6PD) activity (with normal activity defined as >/=70% of the median value determined at each trial site among 36 healthy male volunteers who were otherwise not involved in the trial). All patients received a 3-day course of chloroquine (total dose of 1500 mg). In addition, patients were assigned to receive a single 300-mg dose of tafenoquine on day 1 or 2 (260 patients), placebo (133 patients), or a 15-mg dose of primaquine once daily for 14 days (129 patients). The primary outcome was the Kaplan-Meier estimated percentage of patients who were free from recurrence at 6 months, defined as P. vivax clearance without recurrent parasitemia. RESULTS: In the intention-to-treat population, the percentage of patients who were free from recurrence at 6 months was 62.4% in the tafenoquine group (95% confidence interval [CI], 54.9 to 69.0), 27.7% in the placebo group (95% CI, 19.6 to 36.6), and 69.6% in the primaquine group (95% CI, 60.2 to 77.1). The hazard ratio for the risk of recurrence was 0.30 (95% CI, 0.22 to 0.40) with tafenoquine as compared with placebo (P<0.001) and 0.26 (95% CI, 0.18 to 0.39) with primaquine as compared with placebo (P<0.001). Tafenoquine was associated with asymptomatic declines in hemoglobin levels, which resolved without intervention. CONCLUSIONS: Single-dose tafenoquine resulted in a significantly lower risk of P. vivax recurrence than placebo in patients with phenotypically normal G6PD activity.en_US
dc.identifier.doihttps://doi.org/10.1056/NEJMoa1710775
dc.identifier.scopus2-s2.0-85060126699
dc.identifier.urihttps://hdl.handle.net/20.500.12866/19149
dc.language.isoeng
dc.publisherMassachusetts Medical Society
dc.relation.ispartofurn:issn:1533-4406
dc.relation.ispartofseriesNew England Journal of Medicine
dc.relation.issn1533-4406
dc.rightshttp://purl.org/coar/access_right/c_14cb
dc.subjectadolescenten_US
dc.subjectAdolescenten_US
dc.subjectadulten_US
dc.subjectAdulten_US
dc.subjectaminoquinoline derivativeen_US
dc.subjectAminoquinolinesen_US
dc.subjectantimalarial agenten_US
dc.subjectAntimalarialsen_US
dc.subjectArticleen_US
dc.subjectBrazilen_US
dc.subjectCambodiaen_US
dc.subjectchloroquineen_US
dc.subjectChloroquineen_US
dc.subjectclinical trialen_US
dc.subjectcombination drug therapyen_US
dc.subjectcontrolled studyen_US
dc.subjectCytochrome P-450 CYP2D6en_US
dc.subjectcytochrome P450 2D6en_US
dc.subjectdisease free survivalen_US
dc.subjectdisease severityen_US
dc.subjectDisease-Free Survivalen_US
dc.subjectdizzinessen_US
dc.subjectdouble blind procedureen_US
dc.subjectDouble-Blind Methoden_US
dc.subjectdrug safetyen_US
dc.subjectDrug Therapy, Combinationen_US
dc.subjectenzyme activityen_US
dc.subjectEthiopiaen_US
dc.subjectfemaleen_US
dc.subjectFemaleen_US
dc.subjectG6PD protein, humanen_US
dc.subjectglucose 6 phosphate dehydrogenaseen_US
dc.subjectGlucosephosphate Dehydrogenaseen_US
dc.subjecthematocriten_US
dc.subjecthemoglobinen_US
dc.subjectHemoglobinsen_US
dc.subjecthumanen_US
dc.subjectHumansen_US
dc.subjecthypopigmentationen_US
dc.subjectintention to treat analysisen_US
dc.subjectIntention to Treat Analysisen_US
dc.subjectisolation and purificationen_US
dc.subjectKaplan Meier methoden_US
dc.subjectKaplan-Meier Estimateen_US
dc.subjectkeratopathyen_US
dc.subjectLogistic Modelsen_US
dc.subjectmajor clinical studyen_US
dc.subjectMalaria, Vivaxen_US
dc.subjectmaleen_US
dc.subjectMaleen_US
dc.subjectmetabolismen_US
dc.subjectmethemoglobinen_US
dc.subjectmulticenter studyen_US
dc.subjectparasite clearanceen_US
dc.subjectparasitemiaen_US
dc.subjectParasitemiaen_US
dc.subjectPeruen_US
dc.subjectphase 2 clinical trialen_US
dc.subjectphase 3 clinical trialen_US
dc.subjectPhilippinesen_US
dc.subjectplaceboen_US
dc.subjectPlasmodium vivaxen_US
dc.subjectPlasmodium vivax malariaen_US
dc.subjectprimaquineen_US
dc.subjectPrimaquineen_US
dc.subjectpriority journalen_US
dc.subjectproceduresen_US
dc.subjectrandomized controlled trialen_US
dc.subjectrecurrence risken_US
dc.subjectrelapseen_US
dc.subjectretina diseaseen_US
dc.subjectretinal hypopigmentationen_US
dc.subjectsecondary preventionen_US
dc.subjectSecondary Preventionen_US
dc.subjectsingle drug doseen_US
dc.subjectstatistical modelen_US
dc.subjecttafenoquineen_US
dc.subjectThailanden_US
dc.subjecttreatment durationen_US
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.00
dc.titleSingle-dose tafenoquine to prevent relapse of plasmodium vivax malariaen_US
dc.typeinfo:eu-repo/semantics/article
dc.type.localArtículo de revista
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication

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