The effect of radiotherapy (RT) and chemotherapy (CT) on gonadal function w
as assessed in males treated for a childhood brain tumor not directly invol
ving the hypothalamus/pituitary (HP) axis in a population-based study with
a long follow-up time. All males <15 yr at the time of diagnosis (median: 9
.0 yr, range: 0.8 to 14.9 yr) and diagnosed from January 1970 through Febru
ary 1997 in the eastern part of Denmark and [gte]18 yr at the time of follo
w-up (median: 25.8 yr, range:18.5 to 39.3 yr) were included. Thirty males f
ulfilled the criteria. The median age at time of RT was 9.0 yr (range: 0.8
to 14.9 yr) and the median length of follow-up was 18 yr (range: 2.0 to 28.
0 yr). The biological effective dose of RT was determined to the HP region
and to the spine and expressed in gray because the biological effective dos
e gives a means of expressing the biological effect on normal tissue of dif
ferent dosage schedules in a uniform way. Levels of serum FSH, luteiniziug
hormone (LH), sexual hormone-binding globulin, testosterone, and inhibin B
were measured and compared with healthy age-matched male controls (n = 347)
, and the patients had a GnRH stimulation test performed with determination
of peak FSH and LH.
Patients treated with RT + CT (n = 13), compared with patients treated with
RT only (n = 17), had significantly higher median peak FSH (8.33 vs. 3.79
IU/L, P = 0.03) and median peak LH (20.0 vs. 12.8 IU/L, P = 0.03), and sign
ificantly lower median inhibin. B (86.0 vs. 270 pg/ml, P = 0.03), and media
n inhibin B/FSH ratio (12.8 vs. 107.9, P = 0.04), which indicates gonadal d
amage. Inhibin B and inhibin B/FSH ratio were also significantly lower in t
he RT + CT group, compared with controls (median: 86.0 vs. 215 pg/ml, P = 0
.02), (median:12.8 vs. 67; P = 0.01), respectively. We found a significantl
y inverse correlation between basal FSH and inhibin B and FSH and total tes
ticular volume (r(s) = -0.83; P < 0.0001), (r(s)= -0.67; P < 0.0001), respe
ctively, and a significant correlation between inhibin B and total testicul
ar volume (r(s) = 0.63; P < 0.0001). Stepwise backward multiple linear regr
ession analysis showed the best-fit model to predict inhibin B levels inclu
ded total testicular volume (P = 0.002) and GT (P = 0.09). Median basal LH
in the RT-only group was significantly lower, compared with controls (3.44
vs. 2.45 IU/L; P = 0.0001) indicating secondary hypogonadism, and in both t
he RT + CT group and the RT-only group, levels of testosterone were signifi
cantly lower, compared with our reference population (12.8 vs. 21.9 nmol/L;
P = 0.001, and 14.7 vs. 21.9 nmol/L; P = 0.0003), respectively.
In conclusion these data suggest that cranial irradiation for a childhood b
rain tumor may affect the HP axis, and adjuvant CT can reduce inhibin B ind
icating primary gonadal damage. Thus, such patients may have normal or even
low levels of FSH despite damage to the seminiferous epithelium, and becau
se the fertility status by a semen analysis for psychological reasons can b
e difficult to obtain in this group of patients, we suggest inhibin B as th
e most useful direct serum marker of spermatogenesis in the follow-up of in
dividuals who have received both cranial irradiation and gonadotoxic chemot
herapy. However, because the number of patients with RT + CT and RT only ar
e small, these data must be confirmed in further studies.