GH is increasingly used for treatment of children and adults. It is mitogen
ic, however, and there is therefore concern about its safety, especially wh
en used to treat cancer patients who have become GH deficient after cranial
radiotherapy. We followed 180 children with brain tumors attending three l
arge hospitals in the United Kingdom and treated with GH during 1965-1996,
and 891 children with brain tumors at these hospitals who received radiothe
rapy but not GH. Thirty-five first recurrences occurred in the GH-treated c
hildren and 434 in the untreated children. The relative risk of first recur
rence in GH-treated compared with untreated patients, adjusted for potentia
lly confounding prognostic variables, was decreased (0.6; 95% confidence in
terval, 0.4-0.9) as was the relative risk of mortality (0.5; 95% confidence
interval, 0.3-0.8). There was no significant trend in relative risk of rec
urrence with cumulative time for which GH treatment had been given or with
time elapsed since this treatment started. The relative risk of mortality i
ncreased significantly with time since first GH treatment. The results, bas
ed on much larger numbers than previous studies, suggest that GH does not i
ncrease the risk of recurrence of childhood brain tumors, although the risi
ng trend in mortality relative risks with longer follow-up indicates the ne
ed for continued surveillance.