Sj. Howell et al., Fatigue, sexual function and mood following treatment for haematological malignancy: the impact of mild Leydig cell dysfunction, BR J CANC, 82(4), 2000, pp. 789-793
Fatigue, sexual dysfunction, anxiety and depression are ail more common in
patients who have previously been treated with cytotoxic chemotherapy and r
adiotherapy (XRT) for haematological malignancies, Following therapy, a sig
nificant proportion of men have biochemical evidence of Leydig cell dysfunc
tion, defined by a raised luteinizing hormone level in the presence of a lo
w/normal testosterone level. We postulated that mild testosterone deficienc
y may account for some of the long-term side-effects of treatment, and we h
ave therefore assessed fatigue, mood and sexual function by questionnaire i
n 36 patients with Leydig cell dysfunction (group 1), and also in a group o
f 30 patients (group 2) with normal hormone levels who underwent the same t
reatment for cancer. There was no significant difference in anxiety and dep
ression scores between the two groups although anxiety scores were higher t
han those previously reported for normal men, Eighty seven per cent of grou
p 2 were sexually active compared with only 69% of group 1 (P = 0.1), and p
atients in group 1 engaged less in sexual activity than those in group 2 (m
ean of 1.8 limes per week compared with 3.2 times per week; P = 0.02) Fatig
ue scores were significantly higher in both groups compared with normal men
, but there were no significant differences in any of the fatigue subscales
between the two groups. We conclude that mild Leydig cell insufficiency fo
llowing treatment with cytotoxic chemotherapy +/- XRT is not associated wit
h higher levels of fatigue and anxiety but may result in reduced sexual fun
ction. These results do not provide a convincing argument that androgen rep
lacement therapy is mandatory to improve quality of life in the majority of
these patients, although ii may be beneficial in a minority. To establish
criteria for selection of patients for a trial of androgen therapy a random
ized placebo-controlled study will be necessary. (C) 2000 Cancer Research C
ampaign.