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Protection against vaccine preventable diseases in children treated for acute lymphoblastic leukemia
Author(s) -
de la Fuente Garcia Isabel,
Coïc Léna,
Leclerc JeanMarie,
Laverdière Caroline,
Rousseau Céline,
Ovetchkine Philippe,
Tapiéro Bruce
Publication year - 2017
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.26187
Subject(s) - medicine , measles , vaccination , rubella , poliomyelitis , vaccine preventable diseases , booster dose , pediatrics , chickenpox , diphtheria , vaccination schedule , vaccine failure , hib vaccine , immunization , immunology , antibody , virus , conjugate vaccine
Abstract Background The objective of this retrospective study was to assess protection against vaccine preventable diseases (VPDs) in children treated for acute lymphoblastic leukemia (ALL). Procedure Clinical characteristics and vaccination records were collected. Antibodies against VPDs were measured after completion of chemotherapy and after a booster dose of vaccine. Immunization status of household members was evaluated. Results Sixty children were included. Median interval between the end of chemotherapy and enrolment in the study was 13 months (range 1–145). At ALL diagnosis, 81.3% of the children were up to date with their vaccination schedule. This proportion decreased to 52.9% at enrolment. Among the parents, 21% were up to date with their immunization schedule and 42% had received seasonal influenza vaccination. After chemotherapy, less than 50% of the patients were seroprotected against tetanus, diphtheria, polio 3, Haemophilus influenzae type b (Hib), and mumps and no more than 80% were seroprotected against polio 1 and 2, measles, rubella, and varicella. After a booster dose of vaccine, the rate of protection increased to over 90% for each of the following antigens: TT, DT, polio 1, Hib, measles, and rubella. Nevertheless, polio 3, mumps, and varicella‐zoster virus antibodies titers/concentrations remained below seroprotective thresholds in over 20% of the patients. Conclusions After chemotherapy for ALL, most of the children were not protected against VPDs. As the majority mounted a robust response to booster vaccines, efforts need to be done to improve protection against VPDs by implementing a systematic vaccine booster schedule. This could also be helped by reinforcing household members’ immunization.