Efficacy and Safety of Nifurtimox in Pediatric Patients with Chagas Disease: Results at 4-Year Follow-Up in a Prospective, Historically Controlled Study (CHICO SECURE).
Chagas disease
Trypanosoma cruzi
follow-up
nifurtimox
pediatrics
seronegative conversion
treatment
Journal
Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061
Informations de publication
Date de publication:
18 04 2023
18 04 2023
Historique:
medline:
20
4
2023
pubmed:
29
3
2023
entrez:
28
3
2023
Statut:
ppublish
Résumé
Nifurtimox is recommended for the treatment of Chagas disease; however, long-term follow-up data are scarce. This prolonged follow-up phase of the prospective, historically controlled, CHICO clinical trial evaluated seronegative conversion in pediatric patients aged <18 years with Chagas disease who were followed for 4 years after nifurtimox treatment. Patients were randomly assigned 2:1 to nifurtimox 60-day or 30-day regimens comprising 10 to 20 mg/kg/day for patients aged <12 years and body weight <40 kg, and 8 to 10 mg/kg/day for those aged ≥12 years and body weight ≥40 kg. Anti-Trypanosoma cruzi antibodies decreased during the study period, achieving seronegative conversion in 16 (8.12%) and 8 (8.16%) patients in the 60-day and 30-day nifurtimox regimens, respectively, with corresponding incidence rates per 100 patients/year of seronegative conversion of 2.12 (95% confidence interval [CI]: 1.21 to 3.45) and 2.11 (95% CI: 0.91 to 4.16). Superiority of the 60-day nifurtimox regimen was confirmed by the lower limit of the 95% CI being higher than that (0%) in a historical placebo control group. Children aged <2 years at baseline were more likely to reach seronegative conversion during the 4-year follow-up than older children. At any annual follow-up visit, >90% of evaluable patients had persistently negative quantitative PCR results for T. cruzi DNA. No adverse events potentially related to treatment or caused by protocol-required procedures were documented for either treatment regimen. This study confirms the effectiveness and safety of a pediatric formulation of nifurtimox administered in an age- and weight-adjusted regimen for 60 days to treat children with Chagas disease.
Identifiants
pubmed: 36975790
doi: 10.1128/aac.01193-22
pmc: PMC10112190
doi:
Substances chimiques
Nifurtimox
M84I3K7C2O
Trypanocidal Agents
0
Nitroimidazoles
0
Banques de données
ClinicalTrials.gov
['NCT02625974']
Types de publication
Randomized Controlled Trial
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0119322Références
PLoS Negl Trop Dis. 2021 Oct 4;15(10):e0009801
pubmed: 34606501
N Engl J Med. 2015 Jul 30;373(5):456-66
pubmed: 26222561
Biomed Res Int. 2015;2015:652985
pubmed: 26583124
Lancet Infect Dis. 2018 Apr;18(4):419-430
pubmed: 29352704
Infect Immun. 2011 May;79(5):1855-62
pubmed: 21343357
J Antimicrob Chemother. 2010 Aug;65(8):1759-64
pubmed: 20542903
Lancet. 2019 Apr 13;393(10180):1486-1487
pubmed: 30983574
Am J Trop Med Hyg. 1998 Oct;59(4):526-9
pubmed: 9790423
Rev Inst Med Trop Sao Paulo. 2013;55(3):
pubmed: 23740013
PLoS Negl Trop Dis. 2016 Nov 7;10(11):e0005033
pubmed: 27820837
Pediatr Infect Dis J. 2014 May;33(5):458-62
pubmed: 24153010
PLoS Negl Trop Dis. 2016 Sep 20;10(9):e0004997
pubmed: 27648938
Rev Soc Bras Med Trop. 2007 Jan-Feb;40(1):1-10
pubmed: 17486245
Int J Infect Dis. 2018 Aug;73:93-101
pubmed: 29879524
PLoS Negl Trop Dis. 2021 Jan 7;15(1):e0008912
pubmed: 33412557
Antimicrob Agents Chemother. 2021 Jan 20;65(2):
pubmed: 33168612
Curr Treat Options Infect Dis. 2018;10(3):373-388
pubmed: 30220883
Antimicrob Agents Chemother. 2014;58(2):635-9
pubmed: 24247135
Sci Rep. 2018 Jan 9;8(1):151
pubmed: 29317702
Acta Trop. 2021 Oct;222:106050
pubmed: 34302770
Eur J Pharm Sci. 2021 Nov 1;166:105940
pubmed: 34265407
Lancet Infect Dis. 2021 Aug;21(8):1129-1140
pubmed: 33836161
Clin Infect Dis. 2016 Oct 15;63(8):1056-1062
pubmed: 27432838
Hum Exp Toxicol. 2006 Aug;25(8):471-9
pubmed: 16937919
Mem Inst Oswaldo Cruz. 1999;94 Suppl 1:331-5
pubmed: 10677750
PLoS Negl Trop Dis. 2019 Aug 29;13(8):e0007668
pubmed: 31465522
Lancet Infect Dis. 2015 Nov;15(11):1347-56
pubmed: 26231478
Adv Parasitol. 2017;97:1-45
pubmed: 28325368
J Trop Med. 2012;2012:292138
pubmed: 22523499
Autops Case Rep. 2015 Sep 30;5(3):7-9
pubmed: 26558241
PLoS One. 2019 Aug 21;14(8):e0221100
pubmed: 31433828
PLoS Negl Trop Dis. 2022 Nov 21;16(11):e0010828
pubmed: 36409773
PLoS Negl Trop Dis. 2013;7(1):e2000
pubmed: 23350002
N Engl J Med. 2014 May 15;370(20):1899-908
pubmed: 24827034
Front Public Health. 2019 Jul 02;7:166
pubmed: 31312626
J Am Coll Cardiol. 2017 Feb 28;69(8):939-947
pubmed: 28231946
Acta Trop. 2019 Nov;199:105120
pubmed: 31376368
J Cell Mol Med. 2010 Jun;14(6B):1373-84
pubmed: 20070438
PLoS Negl Trop Dis. 2021 Aug 16;15(8):e0009697
pubmed: 34398888
J Parasitol Res. 2009;2009:463575
pubmed: 20981287
Antimicrob Agents Chemother. 2022 May 17;66(5):e0202121
pubmed: 35416710
Eur Cardiol. 2019 Jul 11;14(2):82-88
pubmed: 31360228