Randomized, Open-Label Trial of Primaquine against Vivax Malaria Relapse in Indonesia

Author:

Sutanto Inge1,Tjahjono Bagus2,Basri Hasan3,Taylor W. Robert3,Putri Fauziah A.3,Meilia Rizka A.3,Setiabudy Rianto1,Nurleila Siti3,Ekawati Lenny L.3,Elyazar Iqbal3,Farrar Jeremy45,Sudoyo Herawati6,Baird J. Kevin35

Affiliation:

1. Faculty of Medicine, University of Indonesia, Jakarta, Indonesia

2. Health Service, Army of the Republic of Indonesia, Jakarta, Indonesia

3. Eijkman-Oxford Clinical Research Unit, Jakarta, Indonesia

4. Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam

5. Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Churchill Hospital, Oxford, United Kingdom

6. Eijkman Institute for Molecular Biology, Jakarta, Indonesia

Abstract

ABSTRACT Radical cure of Plasmodium vivax infection applies blood schizontocidal therapy against the acute attack and hypnozoitocidal therapy against later relapse. Chloroquine and primaquine have been used for 60 years in this manner. Resistance to chloroquine by the parasite now requires partnering other blood schizontocides with primaquine. However, the safety and efficacy of primaquine against relapse when combined with other drugs have not been demonstrated. This randomized, open-label, and relapse-controlled trial estimated the efficacy of primaquine against relapse when administered with quinine or dihydroartemisinin-piperaquine for treatment of the acute infection. Among 650 soldiers who had returned to their malaria-free base in Java, Indonesia, after 12 months in malarious Papua, Indonesia, 143 with acute P. vivax malaria were eligible for study. One hundred sixteen enrolled subjects were randomized to these treatments: artesunate (200-mg dose followed by 100 mg/day for 6 days), quinine (1.8 g/day for 7 days) plus concurrent primaquine (30 mg/day for 14 days), or dihydroartemisinin (120 mg) plus piperaquine (960 mg) daily for 3 days followed 25 days later by primaquine (30 mg/day for 14 days). Follow-up was for 12 months. One hundred thirteen subjects were analyzable. Relapse occurred in 32 of 41 (78%) subjects administered artesunate alone (2.71 attacks/person-year), 7 of 36 (19%) administered quinine plus primaquine (0.23 attack/person-year), and 2 of 36 (6%) administered dihydroartemisinin-piperaquine plus primaquine (0.06 attack/person-year). The efficacy of primaquine against relapse was 92% (95% confidence interval [CI] = 81% to 96%) for quinine plus primaquine and 98% (95% CI = 91% to 99%) for dihydroartemisinin-piperaquine plus primaquine. Antirelapse therapy with primaquine begun a month after treatment of the acute attack with dihydroartemisinin-piperaquine proved safe and highly efficacious against relapse by P. vivax acquired in Papua, Indonesia.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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