Thirteen-Valent Pneumococcal Conjugate Vaccine in Children With Acute Lymphoblastic Leukemia: Protective Immunity Can Be Achieved on Completion of Treatment. (5th October 2019)

• Record Type: Journal Article
• Authors: Bate, Jessica; Borrow, Ray; Chisholm, Julia; Clarke, Stuart C; Dixon, Elizabeth; Faust, Saul N; Galanopoulou, Angeliki; Goldblatt, David; Heath, Paul T; Maishman, Tom; Mapstone, Susan; Patel, Soonie R; Williams, Antony P; Gray, Juliet C
• Is Part Of: Clinical infectious diseases. Volume 71:Number 5(2020)
• Page Start: 1271
• Page End: 1280
• Publication Date: 2019-10-05
• Subjects: acute lymphoblastic leukemia -- pneumococcal conjugate vaccine -- immunization -- immunocompromised; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciz965
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract: Background: Children with acute lymphoblastic leukemia (ALL) are at increased risk of developing invasive pneumococcal disease. This study describes the immunogenicity of 13-valent pneumococcal conjugate vaccine (PCV13) during and after chemotherapy. Methods: Children with ALL were allocated to study groups and received a single dose of PCV13: group 1, maintenance chemotherapy; group 2, end of chemotherapy; group 3, 6 months after chemotherapy. A protective vaccine response was defined as at least 10 of 12 serotypes (or >83% of serotypes with data) achieving postvaccination serotype-specific immunoglobulin G ≥0.35 µg/mL and ≥4-fold rise, compared to prevaccination at 1 and 12 months. Results: One hundred eighteen children were recruited. Only 12.8% (5/39; 95% confidence interval [CI], 4.3%–27.4%) of patients vaccinated during maintenance (group 1) achieved a protective response at 1 month postvaccination and none had a protective response at 12 months. For group 2 patients, 59.5% (22/37; 95% CI, 42.1%–75.3%) achieved a response at 1 month and 37.9% (11/29; 95% CI, 20.7%–57.7%) maintained immunity at 12 months. For group 3 patients, 56.8% (21/37; 95% CI, 39.5%–72.9%) achieved a protective response at 1 month and 43.3% (13/30; 95% CI, 25.5%–62.6%) maintained immunity at 12 months. Conclusions: This study demonstrated that the earliest time point at which protective immunity can be achieved in children with ALL is on completion of chemotherapy. This is earlier than current recommendations and may improve protection during a period when children are most susceptible to infection. Clinical Trials Registration: EudraCT 2009-011587-11. Abstract : Children with acute lymphoblastic leukemia (ALL) can develop invasive pneumococcal disease. This study demonstrated that the immunogenicity of a 13-valent pneumococcal conjugate vaccine on completion of ALL treatment is equivalent to its immunogenicity when given 6 months later, thus providing a rationale for providing earlier protection.