Preventing bone complications in patients with prostate cancer: The emerging role of zoledronic acid

被引:2
|
作者
Saad, F [1 ]
机构
[1] Notre Dame Hosp, Ctr Hosp, Montreal, PQ H2L 4M1, Canada
关键词
bisphosphonates; bone metastases; prostate cancer; quality of life;
D O I
10.1016/j.eursup.2004.08.009
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective: Advances in early detection of disease progression and treatment of advanced disease have prolonged the survival of patients with prostate cancer. However, these patients develop significant skeletal morbidity as a result of bone metastases, and treatment-related bone loss undermines skeletal integrity. This paper reviews the role of bisphosphonates in the treatment of prostate cancer during different stages of the disease. Methods: Published studies were identified through MEDLINE searches, review of bibliographies of relevant articles, and review of abstracts from Scientific meetings. Results: Skeletal complications arising from bone loss occur during several stages of prostate cancer. Zoledronic acid has been shown to increase bone mineral density in men receiving androgen deprivation therapy and is the only bisphosphonate that has demonstrated statistically significant reduction in skeletal morbidity in patients with bone metastases. Recently, an algorithm was developed recommending the use of zoledronic acid for the prevention of skeletal complications arising across the continuum of skeletal complications from treatment-induced bone loss and bone metastases. Conclusions: Zoledronic acid is the only bisphosphonate that has demonstrated effectiveness for increasing bone mass and preventing skeletal complications in patients with prostate cancer. Zoledronic acid should be considered for the treatment and prevention of skeletal morbidity related to prostate cancer. (C) 2004 Published by Elsevier B.V.
引用
下载
收藏
页码:25 / 33
页数:9
相关论文
共 50 条
  • [41] Bone Turnover Markers as Predictors of Mortality Risk in Prostate Cancer Patients with Bone Metastases Following Treatment with Zoledronic Acid
    Jung, Klaus
    Miller, Kurt
    Wirth, Manfred
    Albrecht, Michael
    Lein, Michael
    EUROPEAN UROLOGY, 2011, 59 (04) : 604 - 612
  • [43] Suppression of bone density loss and bone turnover in patients with hormone-sensitive prostate cancer and receiving zoledronic acid
    Ryan, Christopher W.
    Huo, Dezheng
    Bylow, Kathryn
    Demers, Laurence M.
    Stadler, Walter M.
    Henderson, Tara O.
    Vogelzang, Nicholas J.
    BJU INTERNATIONAL, 2007, 100 (01) : 70 - 75
  • [45] The Zotect study: Effect of zoledronic acid (Zometa®) on Bone Metabolism in Patients with Nreast or Prostate cancer with Bone metastases.
    Gschwendt, J.
    Ziller, M.
    Kalder, M.
    Lux, C.
    Maurer, T.
    Muth, M.
    Schmidt, K.
    Hadji, P.
    ONKOLOGIE, 2010, 33 : 204 - 204
  • [46] Zoledronic acid significantly reduces fractures in patients with hormone-refractory prostate cancer metastatic to bone
    Fred, S
    Gleason, D
    Murray, R
    Venner, P
    Tchekmediyian, S
    Chin, J
    Goas, A
    Reitsma, D
    Seaman, J
    JOURNAL OF UROLOGY, 2002, 167 (04): : 175 - 175
  • [47] Zoledronic acid for hormone-naive prostate cancer with bone metastasis.
    Nozawa, Masahiro
    Hara, Isao
    Nagao, Kazuhiro
    Matsuyama, Hideyasu
    Uemura, Hirotsugu
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (15)
  • [48] Effect of zoledronic acid on bone loss associated with androgen blockade for prostate cancer
    Casey, R
    Love, W
    Pearson, D
    Reymond, D
    Zarenda, M
    BONE, 2004, 34 : S84 - S84
  • [49] Zoledronic acid and atrial fibrillation in cancer patients with bone metastases
    Aksoy, S.
    Dizdar, O.
    Turgut, D.
    Dede, D. Sener
    Arslan, C.
    Harputluoglu, H.
    Altundag, K.
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15)
  • [50] An Observational Study of Concomitant Use of Emerging Therapies and Denosumab or Zoledronic Acid in Prostate Cancer
    Liede, Alexander
    Wade, Sally
    Lethen, Jan
    Hernandez, Rohini K.
    Warner, Douglas
    Abernethy, Amy P.
    Finelli, Antonio
    CLINICAL THERAPEUTICS, 2018, 40 (04) : 536 - 549