Parasitología, Hospital de Niños Ricardo Gutiérrez and Instituto Multidisciplinario de Investigacion en Patologias Pediatricas (IMIPP), CONICET-GCBA, Buenos Aires, Argentina.
Centro de Atención e Investigación Médica S.A., Yopal, Colombia.
Antimicrob Agents Chemother. 2023 Apr 18;67(4):e0119322. doi: 10.1128/aac.01193-22. Epub 2023 Mar 28.
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.
硝呋替莫被推荐用于治疗恰加斯病;然而,长期随访数据稀缺。这项前瞻性、历史性对照 CHICO 临床试验的延长随访阶段评估了接受硝呋替莫治疗后 4 年的 <18 岁恰加斯病儿童患者的血清学阴性转换。患者按照 2:1 随机分配至硝呋替莫 60 天或 30 天方案治疗,<12 岁且体重 <40kg 的患者给予 10 至 20mg/kg/天,≥12 岁且体重 ≥40kg 的患者给予 8 至 10mg/kg/天。研究期间,抗 Trypanosoma cruzi 抗体减少,60 天和 30 天硝呋替莫方案组分别有 16(8.12%)和 8(8.16%)例患者血清学阴性转换,相应的每 100 例患者/年血清学阴性转换发生率分别为 2.12(95%置信区间 [CI]:1.21 至 3.45)和 2.11(95% CI:0.91 至 4.16)。60 天硝呋替莫方案的优越性通过 95%CI 的下限高于历史安慰剂对照组(0%)得到证实。基线时年龄 <2 岁的儿童在 4 年随访期间更有可能达到血清学阴性转换。在任何年度随访时,>90%的可评估患者的 T. cruzi DNA 定量 PCR 结果持续阴性。两种治疗方案均未记录到与治疗相关或由方案要求的程序引起的不良事件。本研究证实了一种儿童用硝呋替莫制剂的有效性和安全性,该制剂根据年龄和体重调整方案,使用 60 天治疗恰加斯病儿童。