Bo. Samuelsson et al., GROWTH AND GROWTH-HORMONE SECRETION AFTER TREATMENT FOR CHILDHOOD NON-HODGKINS-LYMPHOMA, Medical and pediatric oncology, 28(1), 1997, pp. 27-34
The aim of this study was to evaluate the growth and growth hormone IC
H) secretion, as assessed by the rate and pattern of secretion, in pat
ients in remission from non-Hodgkin's lymphoma (NHL) who had been trea
ted with corticosteroids and intense chemotherapy. None of the patient
s had received cranial irradiation. Twelve children were investigated
yearly by taking 24-hour GH profiles starting 1 year from the time of
diagnosis. The mean age at onset of the disease was 7.5 years. Another
12 young adults were studied in a cross-sectional manner 4.1-21.3 yea
rs (mean, 9.0 years) after diagnosis of NHL. The mean age at onset of
the disease was 10.7 years. The median height velocity was significant
ly decreased during the 1 st year following diagnosis (standard deviat
ion scores [SDS] -0.15, P<.001), especially during the first 3 months
(SDS -0.75, P<.001) when the most intense treatment was given. During
the 2nd year height velocity was still somewhat reduced (SDS -0.13, P<
.001). However, there was no reduction in final attained height. Spont
aneous CH secretion, in terms of both secretory rate and pulsatile pat
tern, was evaluated by measuring integrated GH concentrations in 20-mi
nute blood samples collected over a 24-hour period. The plasma GH conc
entrations were transformed into GH secretion rates by means of a deco
nvolution technique. Fourier time series analysis was applied to deter
mine possible disturbances of rhythmicity of the GH secretion. The GH
secretion rate and the pulsatile pattern of secretion in the NHL patie
nts were similar to those of the reference population of pubertal matc
hed healthy controls. There was no influence of the age at diagnosis o
r of the time from diagnosis of NHL on the CH secretion rate. Growth i
mpairment in children with a malignant disease treated only with stero
ids and chemotherapy is therefore probably not caused by disturbed GH
secretion, but rather by direct interference with bone growth of the c
ytotoxic drugs used. There was no significant influence on weight gain
during the treatment period so an indirect effect of che chemotherapy
on bone growth through interference with adequate nutrition seems unl
ikely. However, GH secretion was not evaluated during the period of gr
owth retardation, and therefore a transient deficiency was not exclude
d. (C) 1997 Wiley-Liss, Inc.