[Somatostatin analogs for the treatment of advanced, hormone-refractory prostate cancer: a possibility for secondary hormonal ablation?]

Urologe A. 2008 Oct;47(10):1334-8. doi: 10.1007/s00120-008-1781-7.
[Article in German]

Abstract

Almost all patients with hormone-refractory prostate cancer under primary androgen deprivation therapy will develop progression, frequently initially marked by an asymptomatic increase of prostate-specific antigen (PSA). Recent data showed that taxane-based chemotherapy offers significant survival benefit to patients with advanced prostate cancer; however, the toxic side effects frequently exert a significant negative impact on the quality of life. At the androgen-independent stage of the cancer, before becoming hormone refractory, progression might still be delayed by secondary manipulation of either androgen or confounding receptors and their signaling pathways. Secondary hormonal manipulations traditionally included antiandrogen withdrawal, second-line antiandrogens, direct adrenal androgen inhibitors, estrogens, and progestins.We discuss the mode of action and application of somatostatin analogs as an emerging secondary hormonal treatment concept in patients with advanced prostate cancer on the basis of the current literature.

Publication types

  • English Abstract

MeSH terms

  • Androgen Antagonists / administration & dosage
  • Antineoplastic Agents / administration & dosage*
  • Apoptosis / drug effects
  • Bone Neoplasms / drug therapy
  • Bone Neoplasms / secondary
  • Cell Proliferation / drug effects
  • Disease Progression
  • Drug Delivery Systems*
  • Humans
  • Male
  • Neoplasm Staging
  • Neoplasms, Hormone-Dependent / drug therapy*
  • Neoplasms, Hormone-Dependent / mortality
  • Neoplasms, Hormone-Dependent / pathology
  • Prostate-Specific Antigen / drug effects
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / mortality
  • Prostatic Neoplasms / pathology
  • Somatostatin / analogs & derivatives*
  • Somatostatin / therapeutic use
  • Survival Rate

Substances

  • Androgen Antagonists
  • Antineoplastic Agents
  • Somatostatin
  • Prostate-Specific Antigen