S. Polychronopoulouandroulakaki et al., IMMUNE-RESPONSE OF IMMUNOCOMPROMISED CHILDREN WITH MALIGNANCIES TO A RECOMBINANT HEPATITIS-B VACCINE, Pediatric hematology and oncology, 13(5), 1996, pp. 425-431
The aim of this study was to interpret the antibody response to hepati
tis B vaccination following an intensified four-dose schedule in 140 c
ancer patients who presented at our clinic between January 1, 1993 and
December 31, 1994. According to therapy status, the patients were div
ided into two groups: group A consisted of 76 patients undergoing chem
otherapy and group B of 64 patients in complete remission and off trea
tment. The eligibility requirements were negative hepatitis B virus (H
BV), HCV and human immunodeficiency virus serologic markers. A total o
f four doses (20 mu g per dose) of recombinant HB vaccine was administ
ered intramuscularly in the deltoid region at 0, 1, 2, and 6 months. B
lood from the vaccinated subjects was obtained at months 1, 2, 3, and
7 in order to measure anti-HBs titer levels. Protective anti-HBs titer
s were considered to be those greater than or equal to 10 mI/mL. The o
verall seroconversion rate I month after the fourth dose was 57% (80/1
40 patients), and the seroconversion rates for groups A and B were 31.
5% (24/76 patients) and 87.5% (56/64 patients), respectively. Our resu
lts indicated that immunocompromised children undergoing chemotherapy
(although less responsive than children in complete remission and off
treatment) still preserved their potential to produce protective titer
s of anti-HBs. On this basis we recommend (1) HB vaccination after dia
gnosis of malignancy in pediatric patients whenever a high prevalence
of HB infection exists and (2) vaccination of patients off therapy and
in complete remission.