J. Tacke et al., Long-term risk of gastrointestinal tumor recurrence after postoperative treatment with recombinant human growth hormone, J PARENT EN, 24(3), 2000, pp. 140-144
Background: Recombinant human growth hormone (rhGH) promotes protein synthe
sis, accelerates wound healing, and maintains immune function in the catabo
lic state. It has also been claimed that rhGH may promote the activation of
residual tumor cells, and therefore, increases the risk of tumor recurrenc
e. This study aimed to investigate whether postoperative administration of
rhGH increases the long-term risk of tumor recurrences in patients undergoi
ng major gastrointestinal surgery for malignancy. Methods. Patients (n = 10
4) received three different doses of rhGH (0.075 IU/kg, 0.150 IU/kg, and 0.
300 IU/kg) during 5 postoperative days in a placebo-controlled trial. Follo
w-up was per formed for 56-70 months after radical tumor resection. Mean su
rvival period and relapse-free survival were compared with the control grou
p. Results: Complete data were available for 75 patients. Thirty-five perce
nt (n = 20) of all patients treated with rhGH showed tumor recurrences in c
omparison to 44% (n = 8) of patients given placebo. Mean survival period fo
r rhGH-treated patients was 46 months (median 59 months): in controls, 42 m
onths (median 58 months). The length of relapse-free survival tended to be
longer in rhGH-treated patients (2-47 months; median, 21 months) compared w
ith the patients who were given placebo (2-18 months; median, 13 months). C
onclusions: The results demonstrate no evidence for an increased risk of tu
mor recurrence after rhGH treatment for a short period of time after remova
l of a gastrointestinal adenocarcinoma. Therefore, the positive metabolic e
ffects of rhGH application can be used safely in the treatment of the posto
perative catabolic state in the patient groups investigated.