Cluster-randomized trial of monthly malaria prophylaxis versus focused screening and treatment: a study protocol to define malaria elimination strategies in Cambodia

Jessica Manning, Chanthap Lon, Michele Spring, Mariusz Wojnarski, Sok Somethy, Soklyda Chann, Panita Gosi, Kin Soveasna, Sabaithip Sriwichai, Worachet Kuntawunginn, Mark M Fukuda, Philip L Smith, Huy Rekol, Muth Sinoun, Mary So, Jessica Lin, Prom Satharath, David Saunders, Jessica Manning, Chanthap Lon, Michele Spring, Mariusz Wojnarski, Sok Somethy, Soklyda Chann, Panita Gosi, Kin Soveasna, Sabaithip Sriwichai, Worachet Kuntawunginn, Mark M Fukuda, Philip L Smith, Huy Rekol, Muth Sinoun, Mary So, Jessica Lin, Prom Satharath, David Saunders

Abstract

Background: Malaria remains a critical public health problem in Southeast Asia despite intensive containment efforts. The continued spread of multi-drug-resistant Plasmodium falciparum has led to calls for malaria elimination on the Thai-Cambodian border. However, the optimal approach to elimination in difficult-to-reach border populations, such as the Military, remains unclear.

Methods/design: A two-arm, cluster-randomized controlled, open-label pilot study is being conducted in military personnel and their families at focal endemic areas on the Thai-Cambodian border. The primary objective is to compare the effectiveness of monthly malaria prophylaxis (MMP) with dihydroartemisinin-piperaquine and weekly primaquine for 12 weeks compared with focused screening and treating (FSAT) following current Cambodian national treatment guidelines. Eight separate military encampments, making up approximately 1000 military personnel and their families, undergo randomization to the MMP or FSAT intervention for 3 months, with an additional 3 months' follow-up. In addition, each treatment cluster of military personnel and civilians is also randomly assigned to receive either permethrin- or sham (water)-treated clothing in single-blind fashion. The primary endpoint is risk reduction for malaria infection in geographically distinct military encampments based on their treatment strategy. Monthly malaria screening in both arms is done via microscopy, PCR, and rapid diagnostic testing to compare both the accuracy and cost-effectiveness of diagnostic modalities to detect asymptomatic infection. Universal glucose-6-phosphate dehydrogenase (G6PD) deficiency screening is done at entry, comparing the results from a commercially available rapid diagnostic test, the fluorescence spot test, and quantitative testing for accuracy and cost-effectiveness. The comparative safety of the interventions chosen is also being evaluated.

Discussion: Despite the apparent urgency, the key operational elements of proposed malaria elimination strategies in Southeast Asian mobile and migrant populations, including the Military, have yet to be rigorously tested in a well-controlled clinical study. Here, we present a protocol for the primary evaluation of two treatment paradigms - monthly malaria prophylaxis and focused screening and treatment - to achieve malaria elimination in a Cambodian military population. We will also assess the feasibility and incremental benefit of outdoor-biting vector intervention - permethrin-treated clothing. In the process, we aim to define the cost-effectiveness of the inputs required for success including a responsive information system, skilled human resource and laboratory infrastructure requirements, and quality management. Despite being a relatively low transmission area, the complexities of multi-drug-resistant malaria and the movement of vulnerable populations require an approach that is not only technically sound, but simple enough to be achievable.

Trial registration: ClinicalTrials.gov, ID: NCT02653898 . Registered on 13 January 2016.

Keywords: Cambodia; Dihydroartemisinin-piperaquine; Elimination; Malaria; Mass drug administration; Permethrin; Primaquine.

Conflict of interest statement

Authors’ information

JM was formerly with AFRIMS, but she is now supported by the Intramural Research Program of the NIH, NIAID.

Ethics approval and consent to participate

This study was approved by the Institutional Review Board at the Walter Reed Army Institute of Research and the Cambodian National Ethics Committee on Human Research. All study participants will undergo written study consent to participate.

Consent for publication

All authors consent for publication.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Study flow diagram
Fig. 2.
Fig. 2.
Study timeline for monthly malaria prophylaxis (MMP) intervention clusters. *Treat with artesunate and mefloquine. DHA-PIP dihydroartemisinin-piperaquine, GC gametocyte, RDT rapid diagnostic test, PCR polymerase chain reaction, G6PD glucose-6-phosphatase dehydrogenase, CBC complete blood count

References

    1. World Health Organization Global Malaria Programme . World Malaria Report 2013. Geneva: World Health Organization; 2013.
    1. Lon C, et al. Efficacy of two versus three-day regimens of dihydroartemisinin-piperaquine for uncomplicated malaria in military personnel in northern Cambodia: an open-label randomized trial. PLoS One. 2014;9(3):e93138. doi: 10.1371/journal.pone.0093138.
    1. Spring Michele D, Lin Jessica T, Manning Jessica E, Vanachayangkul Pattaraporn, Somethy Sok, Bun Rathvicheth, Se Youry, Chann Soklyda, Ittiverakul Mali, Sia-ngam Piyaporn, Kuntawunginn Worachet, Arsanok Montri, Buathong Nillawan, Chaorattanakawee Suwanna, Gosi Panita, Ta-aksorn Winita, Chanarat Nitima, Sundrakes Siratchana, Kong Nareth, Heng Thay Kheang, Nou Samon, Teja-isavadharm Paktiya, Pichyangkul Sathit, Phann Sut Thang, Balasubramanian Sujata, Juliano Jonathan J, Meshnick Steven R, Chour Char Meng, Prom Satharath, Lanteri Charlotte A, Lon Chanthap, Saunders David L. Dihydroartemisinin-piperaquine failure associated with a triple mutant including kelch13 C580Y in Cambodia: an observational cohort study. The Lancet Infectious Diseases. 2015;15(6):683–691. doi: 10.1016/S1473-3099(15)70049-6.
    1. Noedl H, Se Y, Schaecher K, Smith BL, Socheat D, Fukuda MM. Evidence of artemisinin-resistant malaria in western Cambodia. N Engl J Med. 2008;359(24):2619–2620. doi: 10.1056/NEJMc0805011.
    1. Wongsrichanalai C, Meshnick SR. Declining artesunate-mefloquine efficacy against falciparum malaria on the Cambodia-Thailand border. Emerg Infect Dis. 2008;14(5):716–719. doi: 10.3201/eid1405.071601.
    1. Ashley EA, et al. Spread of artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med. 2014;371(5):411–423. doi: 10.1056/NEJMoa1314981.
    1. Smith C, Whittaker M. Beyond mobile populations: a critical review of the literature on malaria and population mobility and suggestions for future directions. Malar J. 2014;13(1):307. doi: 10.1186/1475-2875-13-307.
    1. Bhumiratana A, Intarapuk A, Sorosjinda-Nunthawarasilp P, Maneekan P, Koyadun S. Border malaria associated with multidrug resistance on Thailand-Myanmar and Thailand-Cambodia borders: transmission dynamic, vulnerability, and surveillance. Biomed Res Int. 2013;2013:e363417. doi: 10.1155/2013/363417.
    1. Wangroongsarb P, Sudathip P, Satimai W. Characteristics and malaria prevalence of migrant populations in malaria-endemic areas along the Thai-Cambodian border. Southeast Asian J Trop Med Public Health. 2012;43(2):261–269.
    1. Lee VJ, et al. Elimination of malaria risk through integrated combination strategies in a tropical military training island. Am J Trop Med Hyg. 2010;82(6):1024–1029. doi: 10.4269/ajtmh.2010.09-0562.
    1. Manning JE, Satharath P, Gaywee J, Lopez MN, Lon C, Saunders DL. Fighting the good fight: the role of militaries in malaria elimination in Southeast Asia. Trends Parasitol. 2014;30(12):571–581. doi: 10.1016/j.pt.2014.10.002.
    1. Martin TCS, Vinetz JM. Asymptomatic Plasmodium vivax parasitaemia in the low-transmission setting: the role for a population-based transmission-blocking vaccine for malaria elimination. Malar J. 2018;17(1):89.
    1. Lin JT, Saunders DL, Meshnick SR. The role of submicroscopic parasitemia in malaria transmission: what is the evidence? Trends Parasitol. 2014;30(4):183–190. doi: 10.1016/j.pt.2014.02.004.
    1. Lindblade KA, Steinhardt L, Samuels A, Kachur SP, Slutsker L. The silent threat: asymptomatic parasitemia and malaria transmission. Expert Rev Anti-Infect Ther. 2013;11(6):623–639. doi: 10.1586/eri.13.45.
    1. Vantaux A, et al. Contribution to malaria transmission of symptomatic and asymptomatic parasite carriers in Cambodia. J Infect Dis. 2018;217(10):1561–1568. doi: 10.1093/infdis/jiy060.
    1. Lin JT, et al. Microscopic Plasmodium falciparum gametocytemia and infectivity to mosquitoes in Cambodia. J Infect Dis. 2016;213(9):1491–1494. doi: 10.1093/infdis/jiv599.
    1. Bousema T, Okell L, Felger I, Drakeley C. Asymptomatic malaria infections: detectability, transmissibility and public health relevance. Nat Rev Microbiol. 2014;12(12):833–840. doi: 10.1038/nrmicro3364.
    1. Okell LC, Bousema T, Griffin JT, Ouédraogo AL, Ghani AC, Drakeley CJ. Factors determining the occurrence of submicroscopic malaria infections and their relevance for control. Nat Commun. 2012;3:1237. doi: 10.1038/ncomms2241.
    1. Hoyer S, et al. Focused Screening and Treatment (FSAT): a PCR-based strategy to detect malaria parasite carriers and contain drug resistant P. falciparum, Pailin, Cambodia. PLoS One. 2012;7(10):e45797. doi: 10.1371/journal.pone.0045797.
    1. Rossi G, et al. Adapting reactive case detection strategies for falciparum malaria in a low-transmission area in Cambodia. Clin Infect Dis. 2018;66(2):296–298. doi: 10.1093/cid/cix781.
    1. Hustedt J, et al. Reactive case-detection of malaria in Pailin Province, Western Cambodia: lessons from a year-long evaluation in a pre-elimination setting. Malar J. 2016;15:132. doi: 10.1186/s12936-016-1191-z.
    1. Snounou G, et al. Biased distribution of msp1 and msp2 allelic variants in Plasmodium falciparum populations in Thailand. Trans R Soc Trop Med Hyg. 1999;93(4):369–374. doi: 10.1016/S0035-9203(99)90120-7.
    1. Mlambo G, Vasquez Y, LeBlanc R, Sullivan D, Kumar N. A filter paper method for the detection of Plasmodium falciparum gametocytes by reverse transcription polymerase chain reaction. Am J Trop Med Hyg. 2008;78(1):114–116. doi: 10.4269/ajtmh.2008.78.114.
    1. Niederwieser I, Felger I, Beck HP. Plasmodium falciparum: expression of gametocyte-specific genes in monolayer cultures and malaria-positive blood samples. Exp Parasitol. 2000;95(3):163–169. doi: 10.1006/expr.2000.4536.
    1. Parobek CM, et al. Selective sweep suggests transcriptional regulation may underlie Plasmodium vivax resilience to malaria control measures in Cambodia. Proc Natl Acad Sci. 2016;113(50):E8096–E8105. doi: 10.1073/pnas.1608828113.
    1. Bharti AR, et al. Experimental infection of the neotropical malaria vector Anopheles darlingi by human patient-derived Plasmodium vivax in the Peruvian Amazon. Am J Trop Med Hyg. 2006;75(4):610–616. doi: 10.4269/ajtmh.2006.75.610.
    1. Okell LC, et al. The potential contribution of mass treatment to the control of Plasmodium falciparum malaria. PLoS One. 2011;6(5):e20179. doi: 10.1371/journal.pone.0020179.
    1. Campbell MK, Thomson S, Ramsay CR, MacLennan GS, Grimshaw JM. Sample size calculator for cluster randomized trials. Comput Biol Med. 2004;34(2):113–125. doi: 10.1016/S0010-4825(03)00039-8.
    1. Delacollette C, et al. Malaria trends and challenges in the Greater Mekong Subregion. Southeast Asian J Trop Med Public Health. 2009;40(4):674–691.
    1. Bustos MD, Wongsrichanalai C, Delacollette C, Burkholder B. Monitoring antimalarial drug efficacy in the Greater Mekong Subregion: an overview of in vivo results from 2008 to 2010. Southeast Asian J Trop Med Public Health. 2013;44 Suppl 1:201–230.
    1. WPRO | Mobile and migrant populations and malaria information systems, WPRO. [Online]. Available at: . Accessed 21 Mar 2018.
    1. White NJ. Does antimalarial mass drug administration increase or decrease the risk of resistance? Lancet Infect Dis. 2017;17(1):e15–e20. doi: 10.1016/S1473-3099(16)30269-9.
    1. Lin JT, Lon C, Spring MD, Sok S, Chann S, Ittiverakul M, Kuntawunginn W, My M, Thay K, Balasubramanian S, Rahman R, Char M, Lanteri CA, Gosi P, Ubalee R, Meshnick SR, Saunders DL. Single dose primaquine to reduce gametocyte carriage and Plasmodium falciparum transmission in Cambodia. PLoS One. 2017; In press, 2017.
    1. Lwin KM, et al. Randomized, double-blind, placebo-controlled trial of monthly versus bimonthly dihydroartemisinin-piperaquine chemoprevention in adults at high risk of malaria. Antimicrob Agents Chemother. 2012;56(3):1571–1577. doi: 10.1128/AAC.05877-11.
    1. Bojang K, et al. A randomised trial to compare the safety, tolerability and efficacy of three drug combinations for intermittent preventive treatment in children. PLoS One. 2010;5(6):e11225. doi: 10.1371/journal.pone.0011225.
    1. Cisse B, et al. Randomized trial of piperaquine with sulfadoxine-pyrimethamine or dihydroartemisinin for malaria intermittent preventive treatment in children. PLoS One. 2009;4(9):e7164. doi: 10.1371/journal.pone.0007164.
    1. Leang R, et al. Efficacy of dihydroartemisinin-piperaquine for treatment of uncomplicated Plasmodium falciparum and Plasmodium vivax in Cambodia, 2008 to 2010. Antimicrob Agents Chemother. 57(2):818–26.
    1. Zwang J, et al. Safety and efficacy of dihydroartemisinin-piperaquine in falciparum malaria: a prospective multi-centre individual patient data analysis. PLoS One. 2009;4(7):e6358. doi: 10.1371/journal.pone.0006358.
    1. Vanachayangkul P, et al. Piperaquine population pharmacokinetics and cardiac safety in Cambodia. Antimicrob Agents Chemother. 2017. 10.1128/AAC.02000-16.
    1. Maude RJ, Nguon C, Dondorp AM, White LJ, White NJ. The diminishing returns of atovaquone-proguanil for elimination of Plasmodium falciparum malaria: modelling mass drug administration and treatment. Malar J. 2014;13:380. doi: 10.1186/1475-2875-13-380.
    1. Tshefu AK, et al. Efficacy and safety of a fixed-dose oral combination of pyronaridine-artesunate compared with artemether-lumefantrine in children and adults with uncomplicated Plasmodium falciparum malaria: a randomised non-inferiority trial. Lancet. 2010;375(9724):1457–1467. doi: 10.1016/S0140-6736(10)60322-4.
    1. Duparc S, et al. Safety and efficacy of pyronaridine-artesunate in uncomplicated acute malaria: an integrated analysis of individual patient data from six randomized clinical trials. Malar J. 2013;12:70. doi: 10.1186/1475-2875-12-70.
    1. Annex I: Summary of Product Characteristics, Pyramax. EMA. . Accessed 11 Oct 2018.
    1. Saunders DL, Vanachayangkul P, Lon C. Dihydroartemisinin-piperaquine failure in Cambodia. N Engl J Med. 2014;371(5):484–485. doi: 10.1056/NEJMc1403007.
    1. Eziefula Alice C, Bousema Teun, Yeung Shunmay, Kamya Moses, Owaraganise Asiphas, Gabagaya Grace, Bradley John, Grignard Lynn, Lanke Kjerstin H W, Wanzira Humphrey, Mpimbaza Arthur, Nsobya Samuel, White Nicholas J, Webb Emily L, Staedke Sarah G, Drakeley Chris. Single dose primaquine for clearance of Plasmodium falciparum gametocytes in children with uncomplicated malaria in Uganda: a randomised, controlled, double-blind, dose-ranging trial. The Lancet Infectious Diseases. 2014;14(2):130–139. doi: 10.1016/S1473-3099(13)70268-8.
    1. Kondrashin A, Baranova AM, Ashley EA, Recht J, White NJ, Sergiev VP. Mass primaquine treatment to eliminate vivax malaria: lessons from the past. Malar J. 2014;13(1):51. doi: 10.1186/1475-2875-13-51.
    1. White NJ. Primaquine to prevent transmission of falciparum malaria. Lancet Infect Dis. 2013;13(2):175–181. doi: 10.1016/S1473-3099(12)70198-6.
    1. Poirot E, Skarbinski J, Sinclair D, Kachur SP, Slutsker L, Hwang J. Mass drug administration for malaria. Cochrane Database Syst Rev. 2013;12:CD008846.
    1. Grimmond TR, Cameron AS. Primaquine-chloroquine prophylaxis against malaria in Southeast-Asian refugees entering South Australia. Med J Aust. 1984;140(6):322–325.
    1. Soto J, Medina F, Dember N, Berman J. Efficacy of permethrin-impregnated uniforms in the prevention of malaria and leishmaniasis in Colombian soldiers. Clin Infect Dis Off Publ Infect Dis Soc Am. 1995;21(3):599–602. doi: 10.1093/clinids/21.3.599.
    1. Durnez L, Mao S, Denis L, Roelants P, Sochantha T, Coosemans M. Outdoor malaria transmission in forested villages of Cambodia. Malar J. 2013;12:329. doi: 10.1186/1475-2875-12-329.
    1. Gryseels C, et al. Re-imagining malaria: heterogeneity of human and mosquito behaviour in relation to residual malaria transmission in Cambodia. Malar J. 2015;14:165. doi: 10.1186/s12936-015-0689-0.
    1. Kimani EW, Vulule JM, Kuria IW, Mugisha F. Use of insecticide-treated clothes for personal protection against malaria: a community trial. Malar J. 2006;5:63. doi: 10.1186/1475-2875-5-63.
    1. Banks SD, Murray N, Wilder-Smith A, Logan JG. Insecticide-treated clothes for the control of vector-borne diseases: a review on effectiveness and safety. Med Vet Entomol. 2014;28 Suppl 1:14–25. doi: 10.1111/mve.12068.
    1. Pinder M, et al. Efficacy of indoor residual spraying with dichlorodiphenyltrichloroethane against malaria in Gambian communities with high usage of long-lasting insecticidal mosquito nets: a cluster-randomised controlled trial. Lancet. 2015;385(9976):1436–1446. doi: 10.1016/S0140-6736(14)61007-2.
    1. Sangoro O, Turner E, Simfukwe E, Miller JE, Moore SJ. A cluster-randomized controlled trial to assess the effectiveness of using 15% DEET topical repellent with long-lasting insecticidal nets (LLINs) compared to a placebo lotion on malaria transmission. Malar J. 2014;13:324. doi: 10.1186/1475-2875-13-324.

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