dc.date.accessioned2019-07-04T17:00:24Z
dc.date.available2019-07-04T17:00:24Z
dc.date.created2019-07-04T17:00:24Z
dc.date.issued2019
dc.identifierhttps://hdl.handle.net/20.500.12866/6905
dc.identifierhttps://doi.org/10.1056/NEJMoa1710775
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.
dc.languageeng
dc.publisherMassachusetts Medical Society
dc.relationNew England Journal of Medicine
dc.relation1533-4406
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectadolescent
dc.subjectAdolescent
dc.subjectadult
dc.subjectAdult
dc.subjectaminoquinoline derivative
dc.subjectAminoquinolines
dc.subjectantimalarial agent
dc.subjectAntimalarials
dc.subjectArticle
dc.subjectBrazil
dc.subjectCambodia
dc.subjectchloroquine
dc.subjectChloroquine
dc.subjectclinical trial
dc.subjectcombination drug therapy
dc.subjectcontrolled study
dc.subjectCytochrome P-450 CYP2D6
dc.subjectcytochrome P450 2D6
dc.subjectdisease free survival
dc.subjectdisease severity
dc.subjectDisease-Free Survival
dc.subjectdizziness
dc.subjectdouble blind procedure
dc.subjectDouble-Blind Method
dc.subjectdrug safety
dc.subjectDrug Therapy, Combination
dc.subjectenzyme activity
dc.subjectEthiopia
dc.subjectfemale
dc.subjectFemale
dc.subjectG6PD protein, human
dc.subjectglucose 6 phosphate dehydrogenase
dc.subjectGlucosephosphate Dehydrogenase
dc.subjecthematocrit
dc.subjecthemoglobin
dc.subjectHemoglobins
dc.subjecthuman
dc.subjectHumans
dc.subjecthypopigmentation
dc.subjectintention to treat analysis
dc.subjectIntention to Treat Analysis
dc.subjectisolation and purification
dc.subjectKaplan Meier method
dc.subjectKaplan-Meier Estimate
dc.subjectkeratopathy
dc.subjectLogistic Models
dc.subjectmajor clinical study
dc.subjectMalaria, Vivax
dc.subjectmale
dc.subjectMale
dc.subjectmetabolism
dc.subjectmethemoglobin
dc.subjectmulticenter study
dc.subjectparasite clearance
dc.subjectparasitemia
dc.subjectParasitemia
dc.subjectPeru
dc.subjectphase 2 clinical trial
dc.subjectphase 3 clinical trial
dc.subjectPhilippines
dc.subjectplacebo
dc.subjectPlasmodium vivax
dc.subjectPlasmodium vivax malaria
dc.subjectprimaquine
dc.subjectPrimaquine
dc.subjectpriority journal
dc.subjectprocedures
dc.subjectrandomized controlled trial
dc.subjectrecurrence risk
dc.subjectrelapse
dc.subjectretina disease
dc.subjectretinal hypopigmentation
dc.subjectsecondary prevention
dc.subjectSecondary Prevention
dc.subjectsingle drug dose
dc.subjectstatistical model
dc.subjecttafenoquine
dc.subjectThailand
dc.subjecttreatment duration
dc.titleSingle-dose tafenoquine to prevent relapse of plasmodium vivax malaria
dc.typeinfo:eu-repo/semantics/article


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