Dosimetry of 188Re-hydroxyethylidene diphosphonate in human prostate cancer skeletal metastases

J Nucl Med. 2003 Jun;44(6):953-60.

Abstract

188Re-Hydroxyethylidene diphosphonate ((188)Re-HEDP) was used in previous studies for the palliative treatment of metastatic bone pain. However, the kinetic and radiation-absorbed doses have not been well documented. Therefore, the aim of this study was to gather dosimetric data for (188)Re-HEDP.

Methods: Thirteen prostate cancer patients with skeletal involvement were treated with 2,700-3,459 MBq (mean dose, 3,120 MBq) (188)Re-HEDP. Patients underwent whole-body scans 3, 20, and 28 h after therapy. The effective half-life, residence time, and radiation-absorbed dose values were calculated for the whole body, bone marrow, kidneys, and bladder as well as for 29 bone metastases. The urinary excretion rate was determined in 6 urine samples of each patient collected over 48 h at 8-h intervals beginning immediately after the administration of (188)Re-HEDP. After injection of (188)Re-HEDP, blood samples were taken weekly for 6 wk, and platelet and leukocyte counts were performed.

Results: The mean effective half-life was 15.9 +/- 3.5 h in bone metastases, 10.9 +/- 2.1 h in the bone marrow, 11.6 +/- 2.1 h in the whole body, 12.7 +/- 2.2 h in the kidneys, and 7.7 +/- 3.4 h in the bladder. The following radiation-absorbed doses were calculated: 3.83 +/- 2.01 mGy/MBq for bone metastases, 0.61 +/- 0.21 mGy/MBq for the bone marrow, 0.07 +/- 0.02 mGy/MBq for the whole body, 0.71 +/- 0.22 mGy/MBq for the kidneys, and 0.99 +/- 0.18 mGy/MBq for the bladder. (188)Re-HEDP showed a rapid urinary excretion within the first 8 h after therapy, with 41% of the (188)Re-HEDP administered being excreted. Forty-eight hours after therapy, the excretion rate was 60% +/- 12%. Only 1 patient showed a decrease of platelet count below 100 x 10(9) counts/L. None of the patients presented with a decrease of leukocyte count below 3.0 x 10(9) counts/L.

Conclusion: (188)Re-HEDP is an effective radiopharmaceutical used in the palliative treatment of metastatic bone pain. The radiation-absorbed dose is acceptable for bone pain palliation with low doses for the normal bone marrow and the whole body.

Publication types

  • Clinical Trial
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Body Burden
  • Bone Marrow / metabolism
  • Bone Neoplasms / metabolism*
  • Bone Neoplasms / secondary*
  • Etidronic Acid / administration & dosage
  • Etidronic Acid / blood
  • Etidronic Acid / pharmacokinetics*
  • Etidronic Acid / urine
  • Half-Life
  • Humans
  • Injections, Intravenous
  • Kidney / metabolism
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Organometallic Compounds
  • Prostatic Neoplasms / pathology*
  • Radiation Dosage
  • Radiometry / methods
  • Rhenium / administration & dosage
  • Rhenium / blood
  • Rhenium / pharmacokinetics*
  • Rhenium / urine
  • Tissue Distribution
  • Urinary Bladder / metabolism
  • Whole-Body Counting / methods*

Substances

  • Organometallic Compounds
  • rhenium-186 HEDP
  • Rhenium
  • Etidronic Acid