This study has examined the effect of prostate cancer on bone matrix f
ormation and mineralisation by osteoblasts, with special reference to
osteomalacia. Sixty-seven patients with prostatic bone metastases unde
rwent transiliac bone biopsy after double tetracycline labelling. Hist
omorphometric analysis was then undertaken in areas distant from, loca
l to and infiltrated by prostate cancer. In bone free of tumour (n = 4
5) and bone surrounding metastases (n = 7) both matrix formation and c
orrected mineral apposition rate were low. By comparison osteoid surfa
ce, osteoid volume and mineral apposition rate were markedly increased
within metastases (tumor-free bone vs. metastatic bone, p < 0.0001),
a finding consistent with a high bone turnover state. Although osteobl
ast function was disturbed both within metastases and in tumour-free a
reas, classical osteomalacia was not associated with prostate cancer.