prostate cancer;
bone metastases;
bone markers;
bisphosponate treatment;
ANDROGEN DEPRIVATION THERAPY;
CARCINOMA;
EFFICACY;
DISEASE;
OSTEOPOROSIS;
RESORPTION;
SURVIVAL;
CARE;
D O I:
10.1002/pros.20917
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
BACKGROUND. Bone turnover markers are helpful to diagnose bone metastases. The aim of this study was to evaluate the usefulness of these markers in Prostate cancer patients with bone metastases before and during the treatment with zoledronic acid as predictive and monitoring tools of skeletal-related events (SRE). METHODS. One hundred seventeen prostate cancer patients with bone metastases and treated with zoledronic acid (4 mg every 4 weeks) were examined. Fifty-six patients were with and 61 patients without SRE during a 60-week study. Total and bone-specific alkaline phosphatase, and amino-terminal procollagen propeptides of type-I-collagen (PINP), crosslinked N-terminal (NTx), cross-linked C-terminal telopeptides of type-l-collagen (ICTP), and C-terminal telopeptides of type-I-collagen as well as prostate-specific antigen (PSA) were measured before and 12, 24, 36, 48, and 60 weeks after starting treatment. RESULTS. Higher baseline concentrations were observed in the SIZE group. The bone markers except for ICTP and tALP decreased to 20-80% of the baseline values at week 12 after the drug administration showing a generally higher decline in the non-SRE group except for NTx. At all time points during treatment higher and increasing concentrations of bone markers were observed in the SIZE group compared with non-SRE group. Cox regression models with clinical data and bone markers showed the baseline NTx concentration as predictor of SREs. During the study, percentage changes of PINP and ICTP were most indicative for SREs. CONCLUSIONS. Bone markers are useful tools to predict and diagnose SRE in prostate cancer patients with bone metastases under receiving zoledronic acid therapy. Prostate 69: 624-632, 2009. (C) 2009 Wiley-Liss, Inc.
机构:
Peter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, AustraliaPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Murray, Robin
Chin, Joseph L.
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机构:
London Hlth Sci Ctr, London, ON, CanadaPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Chin, Joseph L.
Saad, Fred
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机构:
Ctr Hosp Univ Montreal, Hop Notre Dame, Dept Surg Urol, Montreal, PQ, CanadaPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Saad, Fred
Gleason, Donald M.
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机构:Peter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Gleason, Donald M.
Tchekmedyian, N. Simon
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机构:
Pacific Shores Med Grp, Long Beach, CA USAPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Tchekmedyian, N. Simon
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机构:
Lacombe, Louis
Vinholes, Jeferson J.
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机构:
Irmandade Santa Casa Misericordia Porto Alegre, Rio Grande Do Sul, BrazilPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Vinholes, Jeferson J.
Zheng, Ming
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机构:
Novartis Pharmaceut, Novartis Oncol, E Hanover, NJ USAPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
Zheng, Ming
Hei, Yong-Jiang
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机构:
Novartis Pharmaceut, Novartis Oncol, E Hanover, NJ USAPeter MacCallum Canc Inst, Div Hematol & Med Oncol, Melbourne, Vic, Australia
机构:
Duke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USADuke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USA
Reed, SD
Radeva, JI
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机构:Duke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USA
Radeva, JI
Glendenning, GA
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机构:Duke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USA
Glendenning, GA
Saad, F
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机构:Duke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USA
Saad, F
Schulman, KA
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机构:Duke Univ, Med Ctr, Duke Clin Res Inst, Ctr Clin Genet Econ, Durham, NC 27710 USA