Literature DB >> 21599822

Increases in bone turnover marker levels at an early phase after starting zoledronic acid predicts skeletal-related events in patients with prostate cancer with bone metastasis.

Kouji Izumi1, Atsushi Mizokami, Shingo Itai, Takashi Shima, Kazuyoshi Shigehara, Sotaro Miwa, Yuji Maeda, Hiroyuki Konaka, Eitetsu Koh, Mikio Namiki.   

Abstract

OBJECTIVE: To examine whether bone turnover markers could be predictive markers of the probability of newly arising skeletal-related events (SRE) after the start of zoledronic acid treatment in patients with prostate cancer with bone metastasis. PATIENTS AND METHODS: In all, 30 patients with prostate cancer with bone metastasis were treated with zoledronic acid infusion every 4 weeks. Serum C-terminal crosslinking telopeptide of type 1 collagen (1CTP), bone alkaline phosphatase (BAP), and prostate-specific antigen (PSA) levels were measured at the start of zoledronic acid treatment to establish baseline values, and every 4 weeks thereafter. To judge in the early phase whether zoledronic acid is effective in these patients, we retrospectively compared 1CTP, BAP, and PSA levels at 1, 3, and 6 months after starting zoledronic acid treatment with those at baseline.
RESULTS: SRE-free survival of patients with increases of 1CTP levels at 1 and 3 months and BAP levels at 3 months were significantly poorer than those of patients with decreases in 1CTP or BAP levels (P = 0.001, P = 0.042, and P = 0.004, respectively). Overall survival of patients with increases of 1CTP levels at 1 and 3 months and of BAP levels at 6 months were significantly poorer than those of patients with decreases of 1CTP or BAP levels (P = 0.013, P = 0.027, and P = 0.035, respectively).
CONCLUSION: The measurement of 1CTP and BAP levels at an early phase after starting zoledronic acid treatment may be useful for physicians to inform patients of their prognosis and to determine the subsequent treatment plan.
© 2011 THE AUTHORS. BJU INTERNATIONAL © 2011 BJU INTERNATIONAL.

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Year:  2011        PMID: 21599822     DOI: 10.1111/j.1464-410X.2011.10192.x

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  7 in total

1.  Current approaches to bone-targeted therapy in genitourinary malignancies.

Authors:  Peter F Mulders
Journal:  Ther Adv Urol       Date:  2012-10

Review 2.  Zoledronic acid in genitourinary cancer.

Authors:  M A Climent; U Anido; M J Méndez-Vidal; J Puente
Journal:  Clin Transl Oncol       Date:  2013-04-25       Impact factor: 3.405

3.  Risk factors of skeletal-related events in patients with bone metastasis from non-small cell lung cancer undergoing treatment with zoledronate-a post hoc analysis of a randomized clinical trial.

Authors:  Hirotaka Miyashita; Christina Cruz; Cardinale Smith
Journal:  Support Care Cancer       Date:  2020-08-03       Impact factor: 3.603

4.  Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis.

Authors:  Dongyang Li; Hang Lv; Xuanyu Hao; Bin Hu; Yongsheng Song
Journal:  Cancer Manag Res       Date:  2018-08-30       Impact factor: 3.989

5.  Risk factors of skeletal-related events in patients with bone metastatic castration-resistant prostate cancer undergoing treatment with zoledronate.

Authors:  Hirotaka Miyashita; Christina Cruz; Vaibhav Patel
Journal:  Support Care Cancer       Date:  2021-08-10       Impact factor: 3.359

6.  Serum chemokine (CC motif) ligand 2 level as a diagnostic, predictive, and prognostic biomarker for prostate cancer.

Authors:  Kouji Izumi; Atsushi Mizokami; Hsiu-Ping Lin; Hui-Min Ho; Hiroaki Iwamoto; Aerken Maolake; Ariunbold Natsagdorj; Yasuhide Kitagawa; Yoshifumi Kadono; Hiroshi Miyamoto; Chiung-Kuei Huang; Mikio Namiki; Wen-Jye Lin
Journal:  Oncotarget       Date:  2016-02-16

7.  Enzalutamide versus abiraterone as a first-line endocrine therapy for castration-resistant prostate cancer (ENABLE study for PCa): a study protocol for a multicenter randomized phase III trial.

Authors:  Kouji Izumi; Atsushi Mizokami; Mikio Namiki; Shogo Inoue; Nobumichi Tanaka; Yuko Yoshio; Kei Ishibashi; Manabu Kamiyama; Noriyasu Kawai; Hideki Enokida; Takashi Shima; Shizuko Takahara
Journal:  BMC Cancer       Date:  2017-10-10       Impact factor: 4.430

  7 in total

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