Dosimetry of 188Re-hydroxyethylidene diphosphonate in human prostate cancer skeletal metastases
- PMID: 12791825
Dosimetry of 188Re-hydroxyethylidene diphosphonate in human prostate cancer skeletal metastases
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.
Similar articles
-
Bone marrow absorbed dose of rhenium-186-HEDP and the relationship with decreased platelet counts.J Nucl Med. 1996 Jan;37(1):38-41. J Nucl Med. 1996. PMID: 8543998
-
A model-based method for the prediction of whole-body absorbed dose and bone marrow toxicity for 186Re-HEDP treatment of skeletal metastases from prostate cancer.Eur J Nucl Med Mol Imaging. 2003 Aug;30(8):1114-24. doi: 10.1007/s00259-003-1197-y. Epub 2003 May 22. Eur J Nucl Med Mol Imaging. 2003. PMID: 12761596 Clinical Trial.
-
Dosimetric analysis of radioimmunotherapy with 186Re-labeled bivatuzumab in patients with head and neck cancer.J Nucl Med. 2003 Oct;44(10):1690-9. J Nucl Med. 2003. PMID: 14530488 Clinical Trial.
-
Treatment of metastatic bone pain using the bone seeking radiopharmaceutical Re-186-HEDP.Anticancer Res. 1997 May-Jun;17(3B):1773-7. Anticancer Res. 1997. PMID: 9179233 Review.
-
186Re-HEDP for metastatic bone pain in breast cancer patients.Eur J Nucl Med Mol Imaging. 2004 Jun;31 Suppl 1:S162-70. doi: 10.1007/s00259-004-1539-4. Epub 2004 Apr 29. Eur J Nucl Med Mol Imaging. 2004. PMID: 15118846 Review.
Cited by
-
Dosimetry of bone metastases in targeted radionuclide therapy with alpha-emitting (223)Ra-dichloride.Eur J Nucl Med Mol Imaging. 2016 Jan;43(1):21-33. doi: 10.1007/s00259-015-3150-2. Epub 2015 Aug 13. Eur J Nucl Med Mol Imaging. 2016. PMID: 26266887
-
Usefulness of competitive inhibitors of protein binding for improving the pharmacokinetics of 186Re-MAG3-conjugated bisphosphonate (186Re-MAG3-HBP), an agent for treatment of painful bone metastases.Eur J Nucl Med Mol Imaging. 2009 Jan;36(1):115-21. doi: 10.1007/s00259-008-0925-8. Epub 2008 Aug 16. Eur J Nucl Med Mol Imaging. 2009. PMID: 18709369
-
Role of Radionuclide Therapy as Adjuvant to Palliative External Beam Radiotherapy for Painful Multiple Skeletal Metastasis.World J Oncol. 2010 Aug;1(4):158-166. doi: 10.4021/wjon235w. Epub 2010 Aug 29. World J Oncol. 2010. PMID: 29147199 Free PMC article.
-
The radiological response of patients with advanced bone metastases to lutetium-177-labeled DOTA-ibandronic acid assessed by metabolic tumor volume.J Cancer Res Clin Oncol. 2025 Jul 10;151(7):210. doi: 10.1007/s00432-025-06258-y. J Cancer Res Clin Oncol. 2025. PMID: 40634701 Free PMC article.
-
(188)Re-HEDP combined with capecitabine in hormone-refractory prostate cancer patients with bone metastases: a phase I safety and toxicity study.Eur J Nucl Med Mol Imaging. 2009 Sep;36(9):1425-33. doi: 10.1007/s00259-009-1119-8. Epub 2009 Mar 25. Eur J Nucl Med Mol Imaging. 2009. PMID: 19319526 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical