Concomitant i.v. and oral clodronate in the relief of bone pain--a double-blind placebo-controlled study in patients with prostate cancer

Br J Cancer. 1997;76(7):939-42. doi: 10.1038/bjc.1997.488.

Abstract

Fifty-seven patients with advanced prostate cancer resistant to first-line hormonal therapy were treated with estramustine and additionally randomized for treatment with clodronate or placebo. Clodronate treatment was started with 5 days intravenous administration (300 mg day[-1]) and followed by oral treatment (1.6 g day[-1]) for 12 months. Skeletal pain relief was only about 10% better in the clodronate than in the placebo group. The results do not support the superiority of combined intravenous and oral treatment with clodronate compared with oral administration only.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Analgesics, Non-Narcotic / administration & dosage*
  • Analgesics, Non-Narcotic / adverse effects
  • Analgesics, Non-Narcotic / therapeutic use
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / secondary*
  • Clodronic Acid / administration & dosage*
  • Clodronic Acid / adverse effects
  • Clodronic Acid / therapeutic use
  • Collagen / metabolism
  • Double-Blind Method
  • Humans
  • Injections, Intravenous
  • Male
  • Middle Aged
  • Pain / drug therapy*
  • Pain / metabolism
  • Peptide Fragments / blood
  • Procollagen / blood
  • Prospective Studies
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology*

Substances

  • Analgesics, Non-Narcotic
  • Peptide Fragments
  • Procollagen
  • procollagen type I carboxy terminal peptide
  • Clodronic Acid
  • Collagen