Mm. Mustafa et al., IMMUNE RECOVERY IN CHILDREN WITH MALIGNANCY AFTER CESSATION OF CHEMOTHERAPY, Journal of pediatric hematology/oncology, 20(5), 1998, pp. 451-457
Purpose: To study longitudinally the extent and recovery of cellular a
nd humoral immune alterations in children with cancer after completion
of their therapy. Patients and Methods: Using standard immune assays,
cellular and humoral immunity was measured in 43 infants and children
with cancer at completion of therapy and every 3 months thereafter fo
r 1 year. There were 17 patients with acute lymphoblastic leukemia, 9
with Hodgkin disease, and 17 with solid nonhematopoietic tumors. All c
hildren had received standard childhood immunizations before diagnosis
of cancer. Immune assays performed included circulating lymphocyte su
bpopulations, in vitro antigen-induced responses, and total concentrat
ions of serum immunoglobulin G (IgG), IgM, IgA, and IgG subclasses, an
d specific antibodies against diphtheria, tetanus, pertussis, and poli
ovirus types I, II, and III. Results: At completion of therapy, the ma
jority of patients had low circulating lymphocyte subpopulations and a
ntigen-induced responses. Serum antibody concentrations were low in up
to 89% of patients regardless of the underlying malignancy. Although
improvement occurred during the year of follow-up, 35 of 43 (81%) pati
ents continued to exhibit one or more immune abnormalities 9 to 12 mon
ths after cessation of chemotherapy. Younger patients had more persist
ent alterations. Other risk factors studied (including gender, duratio
n of therapy, and underlying malignancy) did not correlate with the se
verity of the immune defects. With the exception of poliovirus antibod
ies, specific antibody titers against common childhood vaccine antigen
s were deficient at completion of therapy and 9 to 12 months later in
a substantial proportion of patients. Conclusion: Children with malign
ancy have persistent specific and nonspecific immune alterations 9 to
12 months after cessation of chemotherapy. The clinical implications o
f these in vitro observations are unclear and require further evaluati
on.