Premium
Serum concentration of type I collagen metabolites as a quantitative marker of bone metastases in patients with prostate carcinoma
Author(s) -
Yoshida Kenichiro,
Sumi Shuhei,
Arai Kyoko,
Koga Fumitaka,
Umeda Hiroshi,
Hosoya Yoshikatsu,
Honda Mikihiko,
Yano Masataka,
Moriguchi Hideo,
Kitahara Satoshi
Publication year - 1997
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/(sici)1097-0142(19971101)80:9<1760::aid-cncr10>3.0.co;2-3
Subject(s) - medicine , prostate carcinoma , pathology , carcinoma , prostate , type i collagen , oncology , cancer
BACKGROUND Bone scans, widely used for the detection of bone metastases from prostate carcinoma, can neither quantitate metastatic lesions nor detect osteolytic lesions. METHODS Serum concentrations of the carboxyterminal propeptide of Type I procollagen (PICP), the carboxyterminal pyridinoline cross‐linked telopeptide of Type I collagen (ICTP), and prostate specific antigen (PSA) were measured by radioimmunoassays in 48 patients with benign prostatic hyperplasia (BPH), 25 patients with prostate carcinoma (PCA) without bone metastases, and 36 patients with PCA and bone metastases. RESULTS Serum concentrations of PICP were significantly higher in patients with PCA with bone metastases than in patients with BPH or PCA without bone metastases. No significant differences were observed between patients with BPH and those with PCA without bone metastases. Serum ICTP concentrations were significantly higher in patients with PCA than in patients with BPH regardless of the presence or absence of bone metastases. Serum concentrations of PICP, ICTP, and PSA correlated significantly with Soloway's grading system for bone scans. The serum concentrations of PICP and ICTP in patients without bone metastases showed a significant downward trend in response to antiandrogen therapy. CONCLUSIONS These observations suggest that the serum concentrations of PICP and ICTP are quantitative markers of bone metastases from PCA when followed serially in individual patients. Cancer 1997; 80:1760‐7. © 1997 American Cancer Society.