Fosmidomycin-clindamycin for plasmodium falciparum infections in African children

被引:91
|
作者
Borrmann, S
Adegnika, AA
Matsiegui, PB
Issifou, S
Schindler, A
Mawili-Mboumba, DP
Baranek, T
Wiesner, J
Jomaa, H
Kremsner, PG
机构
[1] Univ Tubingen, Inst Trop Med, Dept Parasitol, Tubingen, Germany
[2] Albert Schweitzer Hosp, Med Res Unit, Lambarene, Gabon
[3] Univ Giessen, Inst Biochem, Giessen, Germany
来源
JOURNAL OF INFECTIOUS DISEASES | 2004年 / 189卷 / 05期
关键词
D O I
10.1086/381785
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-times-daily treatment regimens of greater than or equal to4 days were required to achieve radical cure, prompting further research to identify and validate a suitable combination partner to enhance its efficacy. Methods. We conducted a randomized, controlled, open-label study to evaluate the efficacy and safety of fosmidomycin combined with clindamycin (n = 12; 30 and 5 mg/kg body weight every 12 h for 5 days, respectively), compared with fosmidomycin alone (n = 12; 30 mg/kg body weight every 12 h for 5 days) and clindamycin alone (n = 12; 5 mg/kg body weight every 12 h for 5 days) for the clearance of asymptomatic Plasmodium falciparum infections in schoolchildren in Gabon aged 7-14 years. Results. Asexual parasites were rapidly cleared in children treated with fosmidomycin-clindamycin (median time, 18 h) and fosmidomycin alone (25 h) but slowly in children treated with clindamycin alone (71 h; P = .004). However, only treatment with fosmidomycin-clindamycin or clindamycin alone led to the radical elimination of asexual parasites as measured by day 14 and 28 cure rates of 100%. Asexual parasites reappeared by day 28 in 7 children who received fosmidomycin (day 14 cure rate, 92% [11/12; day 28 cure rate, 42% [5/12]). All regimens were well tolerated, and no serious adverse events occurred. Conclusion. The combination of fosmidomycin and clindamycin is well tolerated and superior to either agent on its own with respect to the rapid and radical clearance of P. falciparum infections in African children.
引用
收藏
页码:901 / 908
页数:8
相关论文
共 50 条
  • [1] Fosmidomycin-clindamycin for the treatment of Plasmodium falciparum malaria
    Borrmann, S
    Issifou, S
    Esser, G
    Adegnika, AA
    Ramharter, M
    Matsiegui, PB
    Oyakhirome, S
    Mawili-Mboumba, DP
    Missinou, MA
    Kun, JFJ
    Jomaa, H
    Kremsner, PG
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2004, 190 (09): : 1534 - 1540
  • [2] Randomized controlled trial of fosmidomycin-clindamycin versus sulfadoxine-pyrimethamine in the treatment of Plasmodium falciparum malaria
    Oyakhirome, Sunny
    Issifou, Saadou
    Pongratz, Peter
    Barondi, Fortune
    Rarnharter, Michael
    Kun, Juergen F.
    Missinou, Michel A.
    Lell, Bertrand
    Kremsner, Peter G.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (05) : 1869 - 1871
  • [3] Inadequate Efficacy of a New Formulation of Fosmidomycin-Clindamycin Combination in Mozambican Children Less than Three Years Old with Uncomplicated Plasmodium falciparum Malaria
    Lanaspa, Miguel
    Moraleda, Cinta
    Machevo, Sonia
    Gonzalez, Raquel
    Serrano, Beatriz
    Macete, Eusebio
    Cistero, Pau
    Mayor, Alfredo
    Hutchinson, David
    Kremsner, Peter G.
    Alonso, Pedro
    Menendez, Clara
    Bassat, Quique
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (06) : 2923 - 2928
  • [4] OPTIMIZING THE IN VIVO PHARMACODYNAMICS OF THE PLASMODIUM FALCIPARUM APICOPLAST INHIBITORS FOSMIDOMYCIN AND CLINDAMYCIN
    Walker, Leah A.
    Bagonza, Vision
    Sullivan, David J.
    [J]. AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2017, 97 (05): : 496 - 496
  • [5] Assessment of the pharmacokinetics and dynamics of two combination regimens of fosmidomycin-clindamycin in patients with acute uncomplicated falciparum malaria
    Ruangweerayut, Ronnatrai
    Looareesuwan, Sornchai
    Hutchinson, David
    Chauemung, Anurak
    Banmairuroi, Vick
    Na-Bangchang, Kesara
    [J]. MALARIA JOURNAL, 2008, 7 (1)
  • [6] Assessment of the pharmacokinetics and dynamics of two combination regimens of fosmidomycin-clindamycin in patients with acute uncomplicated falciparum malaria
    Ronnatrai Ruangweerayut
    Sornchai Looareesuwan
    David Hutchinson
    Anurak Chauemung
    Vick Banmairuroi
    Kesara Na-Bangchang
    [J]. Malaria Journal, 7
  • [7] Fosmidomycin plus clindamycin for treatment of pediatric patients aged 1 to 14 years with Plasmodium falciparum malaria
    Borrmann, Steffen
    Lundgren, Ingrid
    Oyakhirome, Sunny
    Impouma, Benido
    Matsiegui, Pierre-Blaise
    Adegnika, Ayola A.
    Issifou, Saadou
    Kun, Juergen F. J.
    Hutchinson, David
    Wiesner, Jochen
    Jomaa, Hassan
    Kremsner, Peter G.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (08) : 2713 - 2718
  • [8] Whole-Genome Sequencing to Evaluate the Resistance Landscape Following Antimalarial Treatment Failure With Fosmidomycin-Clindamycin
    Guggisberg, Ann M.
    Sundararaman, Sesh A.
    Lanaspa, Miguel
    Moraleda, Cinta
    Gonzalez, Raquel
    Mayor, Alfredo
    Cistero, Pau
    Hutchinson, David
    Kremsner, Peter G.
    Hahn, Beatrice H.
    Bassat, Quique
    Odom, Audrey R.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2016, 214 (07): : 1085 - 1091
  • [9] Structural basis of fosmidomycin's action on Plasmodium falciparum
    Tanaka, Nobutada
    Umeda, Tomonobu
    Kusakabe, Yoshio
    Nakanishi, Masayuki
    Kitade, Yukio
    Nakamura, Kazuo T.
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2011, 67 : C303 - +
  • [10] CLINDAMYCIN IS EFFECTIVE AGAINST PLASMODIUM-FALCIPARUM BUT NOT AGAINST PLASMODIUM-VIVAX IN MIXED INFECTIONS
    KREMSNER, PG
    ZOTTER, GM
    GRANINGER, W
    ROCHA, RM
    BIENZLE, U
    FELDMEIER, H
    [J]. TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1989, 83 (03) : 332 - 333