Randomized Study of Early versus Late Immunization with Pneumococcal Conjugate Vaccine after Allogeneic Stem Cell Transplantation

被引:93
作者
Cordonnier, Catherine [1 ,2 ]
Labopin, Myriam [3 ,4 ]
Chesnel, Virginie [3 ,4 ]
Ribaud, Patricia [5 ,6 ]
De la Camara, Rafael [8 ]
Martino, Rodrigo [9 ]
Ullmann, Andrew J. [10 ]
Parkkali, Terttu [13 ]
Locasciulli, Anna [14 ]
Yakouben, Karima [7 ]
Pauksens, Karlis [15 ]
Einsele, Hermann [11 ]
Niederwieser, Dietger [12 ]
Apperley, Jane [18 ]
Ljungman, Per [16 ,17 ]
机构
[1] Henri Mondor Teaching Hosp, Dept Hematol, AP HP, Creteil, France
[2] Univ Paris 12, Creteil, France
[3] Univ Paris 06, INSERM,Grp 14, St Antoine Teaching Hosp,Unite Mixte Rech Sante 8, AP HP,European Grp Blood & Marrow Transplantat Da, Paris, France
[4] Univ Paris 06, INSERM, St Antoine Teaching Hosp,Grp 14, AP HP,Study Off,Unite Mixte Rech Sante 893, Paris, France
[5] Univ Paris 07, Paris, France
[6] St Louis Teaching Hosp, AP HP, Dept Hematol & Bone Marrow Transplant, Paris, France
[7] Robert Debre Teaching Hosp, Dept Hematol, Paris, France
[8] Princesa Teaching Hosp, Dept Hematol, Madrid, Spain
[9] St Pau Teaching Hosp, Dept Hematol, Barcelona, Spain
[10] Johannes Gutenberg Univ Teaching Hosp, Mainz, Germany
[11] Univ Hosp, Dept Internal Med, Wurzburg, Germany
[12] Univ Hosp, Div Internal Med 2, Leipzig, Germany
[13] Univ Helsinki, Cent Hosp, Dept Med, Helsinki, Finland
[14] San Camillo Teaching Hosp, Rome, Italy
[15] Univ Uppsala Hosp, Dept Infect Dis, S-75185 Uppsala, Sweden
[16] Karolinska Univ Hosp, Dept Hematol, Stockholm, Sweden
[17] Karolinska Inst, Stockholm, Sweden
[18] Hammersmith Teaching Hosp, Dept Haematol, London, England
关键词
PROTECTIVE ANTIBODY-RESPONSES; POLYSACCHARIDE VACCINES; DONOR IMMUNIZATION; B CONJUGATE; MARROW; RECIPIENTS; IMMUNOGENICITY; DISEASE; INFECTIONS; CHILDREN;
D O I
10.1086/598324
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background. Invasive pneumococcal disease is a life-threatening complication after allogeneic stem cell transplantation, and at least 20% of cases occur within 1 year after transplantation. The 23-valent pneumococcal polysaccharide vaccine (PPV23) has limited efficacy, especially during the first year after transplantation. The immune response to the conjugated vaccines is expected to be better than that to the polysaccharide vaccine, but the optimal timing of vaccination is not defined. Our objective was to show that a 7-valent pneumococcal conjugate vaccine (PCV7; Prevnar) was not inferior when first given 3 months after transplantation, compared with when first given 9 months after transplantation. Methods. We performed a multicenter, randomized, noninferiority study involving 158 patients from 13 European Group for Blood and Marrow Transplantation centers who were randomly allocated at similar to 100 days after myeloablative stem cell transplantation to receive a series of vaccinations (3 doses of PCV7 given 1 month apart) that was started immediately (i.e., 3 months after transplantation) or 6 months later (i.e., 9 months after transplantation). The primary evaluation criterion was the rate of response (antibody level, similar to 0.15 mg/mL for each of the 7 serotypes) at 1 month after the third dose of PCV7. The noninferiority margin was 20%. All patients were followed up for 24 months after transplantation or until death, whichever occurred first. Results. We found that the response rate was not lower after early vaccination (79% [45 of 57 patients]) than after late vaccination (82% [47 of 57 patients]) (difference, -3.5%; 90% confidence interval, -15.6 to 8.6; not significant). Conclusions. We conclude that PCV7 vaccination at 3 months after stem cell transplantation is not inferior to PCV7 vaccination at 9 months after transplantation. Because invasive pneumococcal disease can occur early, we recommend starting the PCV7 vaccination series at 3 months after transplantation to ensure earlier protection against Streptococcus pneumoniae. However, the early vaccination may result in only short-lasting response and may not prime for a 23-valent pneumococcal polysaccharide vaccine boost as efficiently as the late vaccination.
引用
收藏
页码:1392 / 1401
页数:10
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