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口服减毒活轮状病毒疫苗对拉丁美洲婴儿出生后头两年轮状病毒肠胃炎的疗效和安全性:一项随机、双盲、安慰剂对照的III期研究。

Efficacy and safety of an oral live attenuated human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in Latin American infants: a randomised, double-blind, placebo-controlled phase III study.

作者信息

Linhares Alexandre C, Velázquez F Raúl, Pérez-Schael Irene, Sáez-Llorens Xavier, Abate Hector, Espinoza Felix, López Pío, Macías-Parra Mercedes, Ortega-Barría Eduardo, Rivera-Medina Doris Maribel, Rivera Luis, Pavía-Ruz Noris, Nuñez Ernesto, Damaso Silvia, Ruiz-Palacios Guillermo M, De Vos Béatrice, O'Ryan Miguel, Gillard Paul, Bouckenooghe Alain

机构信息

Instituto Evandro Chagas, Secretaria de Vigilância em Saúde, Ministry of Health, Belém, Pará, Brazil.

出版信息

Lancet. 2008 Apr 5;371(9619):1181-9. doi: 10.1016/S0140-6736(08)60524-3.

Abstract

BACKGROUND

Peak incidence of rotavirus gastroenteritis is seen in infants between 6 and 24 months of age. We therefore aimed to assess the 2-year efficacy and safety of an oral live attenuated human rotavirus vaccine for prevention of severe gastroenteritis in infants.

METHODS

15 183 healthy infants aged 6-13 weeks from ten Latin American countries randomly assigned in a 1 to 1 ratio to receive two oral doses of RIX4414 or placebo at about 2 and 4 months of age in a double-blind, placebo-controlled phase III study were followed up until about 2 years of age. Primary endpoint was vaccine efficacy from 2 weeks after dose two until 1 year of age. Treatment allocation was concealed from investigators and parents of participating infants. Efficacy follow-up for gastroenteritis episodes was undertaken from 2 weeks after dose two until about 2 years of age. Analysis was according to protocol. This study is registered with ClinicalTrials.gov, number NCT00140673 (eTrack444563-023).

FINDINGS

897 infants were excluded from the according-to-protocol analysis. Fewer cases (p<0.0001) of severe rotavirus gastroenteritis were recorded for the combined 2-year period in the RIX4414 group (32 [0.4%] of 7205; 95% CI 0.3-0.6) than in the placebo group (161 [2.3%] of 7081; 1.9-2.6), resulting in a vaccine efficacy of 80.5% (71.3-87.1) to 82.1% (64.6-91.9) against wild-type G1, 77.5% (64.7-86.2) against pooled non-G1 strains, and 80.5% (67.9-88.8) against pooled non-G1 P[8] strains. Vaccine efficacy for hospital admission for rotavirus gastroenteritis was 83.0% (73.1-89.7) and for admission for diarrhoea of any cause was 39.3% (29.1-48.1). No cases of intussusception were reported during the second year of follow-up.

INTERPRETATION

Two doses of RIX4414 were effective against severe rotavirus gastroenteritis during the first 2 years of life in a Latin American setting. Inclusion of RIX4414 in routine paediatric immunisations should reduce the burden of rotavirus gastroenteritis worldwide.

摘要

背景

轮状病毒肠胃炎的发病高峰出现在6至24个月大的婴儿中。因此,我们旨在评估一种口服减毒活人类轮状病毒疫苗预防婴儿严重肠胃炎的2年疗效和安全性。

方法

在一项双盲、安慰剂对照的III期研究中,来自十个拉丁美洲国家的15183名6至13周龄的健康婴儿按1:1的比例随机分配,在大约2个月和4个月大时接受两剂RIX4414或安慰剂,随访至大约2岁。主要终点是从第二剂接种后2周直至1岁的疫苗效力。参与研究的婴儿的研究者和家长均不知晓治疗分配情况。对肠胃炎发作的效力随访从第二剂接种后2周开始,直至大约2岁。分析按照方案进行。本研究已在ClinicalTrials.gov注册,编号为NCT00140673(eTrack444563-023)。

结果

897名婴儿被排除在符合方案分析之外。在RIX4414组中,2年合并期内记录的严重轮状病毒肠胃炎病例(7205例中的32例[0.4%];95%置信区间0.3 - 0.6)少于安慰剂组(7081例中的161例[2.3%];1.9 - 2.6)(p<0.0001),针对野生型G1的疫苗效力为80.5%(71.3 - 87.1)至82.1%(64.6 - 91.9),针对非G1毒株合并株的效力为77.5%(64.7 - 86.2),针对非G1 P[8]毒株合并株的效力为80.5%(67.9 - 88.8)。因轮状病毒肠胃炎住院的疫苗效力为83.0%(73.1 - 89.7),因任何原因腹泻住院的效力为39.3%(29.1 - 48.1)。随访的第二年未报告肠套叠病例。

解读

在拉丁美洲环境下,两剂RIX4414在生命的前2年对严重轮状病毒肠胃炎有效。将RIX4414纳入常规儿科免疫接种应可减轻全球轮状病毒肠胃炎的负担。

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