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

被引:307
作者
Linhares, Alexandre C. [2 ]
Velazquez, F. Raul [3 ]
Perez-Schael, Irene [4 ]
Saez-Llorens, Xavier [5 ]
Abate, Hector [6 ]
Espinoza, Felix [7 ]
Lopez, Pio [8 ]
Macias-Parra, Mercedes [9 ]
Ortega-Barria, Eduardo [10 ]
Rivera-Medina, Doris Maribel [11 ]
Rivera, Luis [12 ]
Pavia-Ruz, Noris [13 ]
Nunez, Ernesto [14 ]
Damaso, Silvia [16 ]
Ruiz-Palacios, Guillermo M. [15 ]
De Vos, Beatrice [16 ]
O'Ryan, Miguel [1 ]
Gillard, Paul [16 ]
Bouckenooghe, Alain [16 ]
机构
[1] Univ Chile, Microbiol & Mycol Programme, Inst Biomed Sci, Fac Med, Santiago, Chile
[2] Minist Hlth, Inst Evandro Chagas, Secretaria Vigilancia Saude, Belem, Para, Brazil
[3] Inst Mexicano Seguro Social, Med Res Unit Infect Dis, Paediat Hosp, Natl Med Ctr SXXI, Mexico City, DF, Mexico
[4] Inst Biomed Fuvesin, Secc Enfermedades Entericas, Caracas, Venezuela
[5] Hosp Nino, Panama City, Panama
[6] Hosp Dr Humberto Notti, Mendoza, Argentina
[7] Univ Nacl Autonoma Leon, Leon, Nicaragua
[8] Clin Materno Infantil Farallones, Cali, Colombia
[9] Inst Nacl Pediat, Mexico City, DF, Mexico
[10] Inst Invest Cientificas Avanzadas & Serv Alta Tec, Panama City, Panama
[11] Hosp Especialidades Ctr Med La Raza, Inst Hondureno Seguridad Social, Tegucigalpa, Honduras
[12] Hosp Nuestra Senora Altagracia, Santo Domingo, Dominican Rep
[13] Univ Nacl Autonoma Mexico, Dept Expt Med, Mexico City 04510, DF, Mexico
[14] Univ Concepcion, Concepcion, Chile
[15] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Infect Dis, Mexico City, DF, Mexico
[16] GlaxoSmithKline Biol, Rixensart, Belgium
关键词
D O I
10.1016/S0140-6736(08)60524-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 15183 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[81 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.
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收藏
页码:1181 / 1189
页数:9
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